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<table width="100%"><col width="70%"/><col width="30%"/><tbody><tr><td valign="top"><paragraph>Warnings and Precautions (<linkHtml href="#S5.3">5.3</linkHtml>)</paragraph></td><td align="right" valign="top"><paragraph>10/2025</paragraph></td></tr></tbody></table>

1 INDICATIONS AND USAGE JARDIANCE is indicated: • to reduce the risk of cardiovascular death and hospitalization for heart failure in adults with heart failure. • to reduce the risk of sustained decline in eGFR, end-stage kidney disease, cardiovascular death, and hospitalization in adults with chronic kidney disease at risk of progression. • to reduce the risk of cardiovascular death in adults with type 2 diabetes mellitus and established cardiovascular disease. • as an adjunct to diet and exercise to improve glycemic control in adults and pediatric patients aged 10 years and older with type 2 diabetes mellitus. JARDIANCE is a sodium-glucose co-transporter 2 (SGLT2) inhibitor indicated: • To reduce the risk of cardiovascular death and hospitalization for heart failure in adults with heart failure. ( 1 ) • To reduce the risk of sustained decline in eGFR, end-stage kidney disease, cardiovascular death, and hospitalization in adults with chronic kidney disease at risk of progression. ( 1 ) • To reduce the risk of cardiovascular death in adults with type 2 diabetes mellitus and established cardiovascular disease. ( 1 ) • As an adjunct to diet and exercise to improve glycemic control in adults and pediatric patients aged 10 years and older with type 2 diabetes mellitus. ( 1 ) Limitations of Use: • Not recommended for use to improve glycemic control in patients with type 1 diabetes mellitus. It may increase the risk of diabetic ketoacidosis in these patients. ( 1 ) • Not recommended for use to improve glycemic control in patients with type 2 diabetes mellitus with an eGFR less than 30 mL/min/1.73 m 2 . ( 1 ) • Not recommended for the treatment of chronic kidney disease in patients with polycystic kidney disease or patients requiring or with a recent history of intravenous immunosuppressive therapy or greater than 45 mg of prednisone or equivalent for kidney disease. JARDIANCE is not expected to be effective in these populations. ( 1 ) Limitations of Use JARDIANCE is not recommended for use to improve glycemic control in patients with type 1 diabetes mellitus. It may increase the risk of diabetic ketoacidosis in these patients [see Warnings and Precautions (5.1) ] . JARDIANCE is not recommended for use to improve glycemic control in patients with type 2 diabetes mellitus with an eGFR less than 30 mL/min/1.73 m 2 . JARDIANCE is likely to be ineffective in this setting based upon its mechanism of action. JARDIANCE is not recommended for the treatment of chronic kidney disease in patients with polycystic kidney disease or patients requiring or with a recent history of intravenous immunosuppressive therapy or greater than 45 mg of prednisone or equivalent for kidney disease [see Clinical Studies (14.5) ] . JARDIANCE is not expected to be effective in these populations.

2 DOSAGE AND ADMINISTRATION • Assess renal function before initiating and as clinically indicated. Assess volume status and correct volume depletion before initiating. ( 2.1 ) • Recommended dosage is 10 mg orally once daily in the morning, taken with or without food. ( 2.2 ) • For additional glycemic control, dosage may be increased to 25 mg orally once daily in patients tolerating JARDIANCE. ( 2.2 ) • Withhold JARDIANCE for at least 3 days, if possible, prior to surgery or procedures associated with prolonged fasting. ( 2.3 ) 2.1 Testing Prior to Initiation of JARDIANCE • Assess renal function before initiating JARDIANCE and as clinically indicated [see Warnings and Precautions (5.2) ] . o Use for glycemic control is not recommended in patients with an eGFR less than 30 mL/min/1.73 m 2 [see Use in Specific Populations (8.6) ]. • Assess volume status. In patients with volume depletion, correct this condition before initiating JARDIANCE [see Warnings and Precautions (5.2) and Use in Specific Populations (8.5 , 8.6) ]. 2.2 Recommended Dosage Table 1 presents the recommended dosage of JARDIANCE in adult and pediatric patients aged 10 years and older. Table 1 Recommended Dosage of JARDIANCE Population Indication Recommended Dosage Adults Reduce the risk of cardiovascular death and hospitalization in patients with heart failure • 10 mg orally once daily in the morning, taken with or without food. Reduce the risk of sustained decline in eGFR, end-stage kidney disease, cardiovascular death, and hospitalization in adults with chronic kidney disease at risk of progression. Reduce the risk of cardiovascular death in patients with type 2 diabetes mellitus with established cardiovascular disease Glycemic control in type 2 diabetes mellitus • 10 mg orally once daily in the morning, taken with or without food. • For additional glycemic control, may increase to 25 mg orally once daily in patients tolerating 10 mg once daily. Pediatric patients aged 10 years and older Glycemic control in type 2 diabetes mellitus • 10 mg orally once daily in the morning, taken with or without food. • For additional glycemic control, may increase to 25 mg orally once daily in patients tolerating 10 mg once daily. 2.3 Temporary Interruption for Surgery Withhold JARDIANCE for at least 3 days, if possible, prior to surgery or procedures associated with prolonged fasting. Resume JARDIANCE when the patient is clinically stable and has resumed oral intake [see Warnings and Precautions (5.1) and Clinical Pharmacology (12.2) ]. 2.4 Recommendations Regarding Missed Dose • If a dose is missed, instruct patients to take the dose as soon as possible. • Advise patients not to double up the next dose.

3 DOSAGE FORMS AND STRENGTHS JARDIANCE tablets available as: • 10 mg pale yellow, round, biconvex and bevel-edged, film-coated tablets debossed with "S 10" on one side and the Boehringer Ingelheim company symbol on the other side. • 25 mg pale yellow, oval, biconvex, film-coated tablets debossed with "S 25" on one side and the Boehringer Ingelheim company symbol on the other side. Tablets: 10 mg, 25 mg ( 3 )

4 CONTRAINDICATIONS JARDIANCE is contraindicated in patients: • with a hypersensitivity to empagliflozin or any of the excipients in JARDIANCE, reactions such as angioedema have occurred [see Warnings and Precautions (5.6) ] . • Hypersensitivity to empagliflozin or any of the excipients in JARDIANCE. ( 4 )

5 WARNINGS AND PRECAUTIONS • Diabetic Ketoacidosis in Patients with Type 1 Diabetes Mellitus and Other Ketoacidosis: Consider ketone monitoring in patients with type 1 diabetes mellitus and consider ketone monitoring in others at risk for ketoacidosis, as indicated. Assess for ketoacidosis regardless of presenting blood glucose levels and discontinue JARDIANCE if ketoacidosis is suspected. Monitor patients for resolution of ketoacidosis before restarting. ( 5.1 ) • Volume Depletion: Before initiating JARDIANCE, assess volume status and renal function in patients with impaired renal function, elderly patients, or patients on loop diuretics. Monitor for signs and symptoms during therapy. ( 5.2 ) • Genitourinary Infections, including Urosepsis, Pyelonephritis, Necrotizing Fasciitis of the Perineum (Fournier's Gangrene), and Genital Mycotic Infections: Monitor patients for signs and symptoms of genitourinary infections and treat promptly, if indicated. Immediately evaluate patients presenting with pain or tenderness, erythema, or swelling in the genital or perineal area, along with fever or malaise, for necrotizing fasciitis and if suspected, discontinue JARDIANCE, and promptly institute appropriate medical and/or surgical intervention. ( 5.3 ) • Hypoglycemia: Adult patients taking an insulin secretagogue or insulin may have an increased risk of hypoglycemia. In pediatric patients 10 years of age and older, the risk of hypoglycemia was higher regardless of insulin use. Consider lowering the dosage of insulin secretagogue or insulin to reduce the risk of hypoglycemia when initiating JARDIANCE. ( 5.4 ) • Lower Limb Amputation: Monitor patients for infections or ulcers of lower limbs, and institute appropriate treatment ( 5.5 ) • Hypersensitivity Reactions: Serious hypersensitivity reactions (e.g., angioedema) have occurred with JARDIANCE. If hypersensitivity reactions occur, discontinue JARDIANCE, treat promptly, and monitor until signs and symptoms resolve. ( 5.6 ) 5.1 Diabetic Ketoacidosis in Patients with Type 1 Diabetes Mellitus and Other Ketoacidosis In patients with type 1 diabetes mellitus, JARDIANCE significantly increases the risk of diabetic ketoacidosis, a life-threatening event, beyond the background rate. In placebo-controlled trials of patients with type 1 diabetes mellitus, the risk of ketoacidosis was markedly increased in patients who received sodium glucose co-transporter 2 (SGLT2) inhibitors compared to patients who received placebo and fatal ketoacidosis has occurred with JARDIANCE. JARDIANCE is not indicated for glycemic control in patients with type 1 diabetes mellitus. Type 2 diabetes mellitus and pancreatic disorders (e.g., history of pancreatitis or pancreatic surgery) are also risk factors for ketoacidosis. There have been postmarketing reports of fatal events of ketoacidosis in patients with type 2 diabetes mellitus using SGLT2 inhibitors, including JARDIANCE. Precipitating conditions for diabetic ketoacidosis or other ketoacidosis include under-insulinization due to insulin dose reduction or missed insulin doses, acute febrile illness, reduced caloric intake, ketogenic diet, surgery, volume depletion, and alcohol abuse. Signs and symptoms are consistent with dehydration and severe metabolic acidosis and include nausea, vomiting, abdominal pain, generalized malaise, and shortness of breath.

ose reduction or missed insulin doses, acute febrile illness, reduced caloric intake, ketogenic diet, surgery, volume depletion, and alcohol abuse. Signs and symptoms are consistent with dehydration and severe metabolic acidosis and include nausea, vomiting, abdominal pain, generalized malaise, and shortness of breath. Blood glucose levels at presentation may be below those typically expected for diabetic ketoacidosis (e.g., less than 250 mg/dL). Ketoacidosis and glucosuria may persist longer than typically expected. Urinary glucose excretion persists for 3 days after discontinuing JARDIANCE [see Clinical Pharmacology (12.2) ] ; however, there have been postmarketing reports of ketoacidosis and/or glucosuria lasting greater than 6 days and some up to 2 weeks after discontinuation of SGLT2 inhibitors. Consider ketone monitoring in patients with type 1 diabetes mellitus and consider ketone monitoring in others at risk for ketoacidosis if indicated by the clinical situation. Assess for ketoacidosis regardless of presenting blood glucose levels in patients who present with signs and symptoms consistent with severe metabolic acidosis. If ketoacidosis is suspected, discontinue JARDIANCE, promptly evaluate, and treat ketoacidosis, if confirmed. Monitor patients for resolution of ketoacidosis before restarting JARDIANCE. Withhold JARDIANCE, if possible, in temporary clinical situations that could predispose patients to ketoacidosis. Resume JARDIANCE when the patient is clinically stable and has resumed oral intake [see Dosage and Administration (2.3) ] . Educate all patients on the signs and symptoms of ketoacidosis and instruct patients to discontinue JARDIANCE and seek medical attention immediately if signs and symptoms occur. 5.2 Volume Depletion JARDIANCE can cause intravascular volume depletion which may sometimes manifest as symptomatic hypotension or acute transient changes in creatinine [see Adverse Reactions (6.1) ] . There have been post-marketing reports of acute kidney injury, some requiring hospitalization and dialysis, in patients with type 2 diabetes mellitus receiving SGLT2 inhibitors, including JARDIANCE. Patients with impaired renal function (eGFR less than 60 mL/min/1.73 m 2 ), elderly patients, or patients on loop diuretics may be at increased risk for volume depletion or hypotension. Before initiating JARDIANCE in patients with one or more of these characteristics, assess volume status and renal function. In patients with volume depletion, correct this condition before initiating JARDIANCE. Monitor for signs and symptoms of volume depletion, and renal function after initiating therapy. 5.3 Genitourinary Infections, including Urosepsis, Pyelonephritis, Necrotizing Fasciitis of the Perineum (Fournier's Gangrene), and Genital Mycotic Infections JARDIANCE increases urinary glucose excretion [see Clinical Pharmacology (12.2) ] and increases the risk of genitourinary infections including urinary tract infections and genital mycotic infections in both male and female patients [see Adverse Reactions (6.1) ] . Serious genitourinary infections, including urosepsis, pyelonephritis, and necrotizing fasciitis of the perineum (Fournier's gangrene, a rare life-threatening infection requiring urgent surgical intervention), have occurred in patients with and without diabetes mellitus receiving SGLT2 inhibitors, including JARDIANCE [see Adverse Reactions (6.2) ]. Cases have required hospitalization. In patients with Fournier's gangrene, serious outcomes have included multiple surgeries and death. Patients with a history of chronic or recurrent genitourinary infections are more likely to develop genitourinary infections when using JARDIANCE. Monitor patients for signs and symptoms of genitourinary infections and treat promptly, if indicated.

gangrene, serious outcomes have included multiple surgeries and death. Patients with a history of chronic or recurrent genitourinary infections are more likely to develop genitourinary infections when using JARDIANCE. Monitor patients for signs and symptoms of genitourinary infections and treat promptly, if indicated. Immediately evaluate patients presenting with pain or tenderness, erythema, or swelling in the genital or perineal area, along with fever or malaise, for necrotizing fasciitis. If suspected, discontinue JARDIANCE and promptly institute appropriate medical and/or surgical intervention. 5.4 Hypoglycemia Insulin and insulin secretagogues are known to cause hypoglycemia. In adult patients, the risk of hypoglycemia may be increased when JARDIANCE is used in combination with insulin secretagogues (e.g., sulfonylurea) or insulin. In pediatric patients aged 10 years and older, the risk of hypoglycemia was higher with JARDIANCE regardless of insulin use [see Adverse Reactions (6.1) ] . The risk of hypoglycemia may be lowered by a reduction in the dose of sulfonylurea (or other concomitantly administered insulin secretagogues) or insulin. Inform patients using these concomitant medications and pediatric patients of the risk of hypoglycemia and educate them on the signs and symptoms of hypoglycemia. 5.5 Lower Limb Amputation In some clinical studies with SGLT2 inhibitors an imbalance in the incidence of lower limb amputation has been observed. Across four JARDIANCE outcome trials, lower limb amputation event rates were 4.3 and 5.0 events per 1,000 patient-years in the placebo group and the JARDIANCE 10 mg or 25 mg dose group, respectively, with a HR of 1.05 (95 % CI) (0.81, 1.36). In a long-term cardio-renal outcome trial [see Clinical Studies 14.5 ] , in patients with chronic kidney disease, the occurrence of lower limb amputations was reported with event rates of 2.9, and 4.3 events per 1,000 patient-years in the placebo, and JARDIANCE 10 mg treatment arms, respectively. Amputation of the toe and mid-foot were most frequent (21 out of 28 JARDIANCE 10 mg treated patients with lower limb amputations), and some involving above and below the knee. Some patients had multiple amputations. Peripheral artery disease, and diabetic foot infection (including osteomyelitis), were the most common precipitating medical events leading to the need for an amputation. The risk of amputation was highest in patients with a baseline history of diabetic foot, peripheral artery disease (including previous amputation) or diabetes. Counsel patients about the importance of routine preventative foot care. Monitor patients receiving JARDIANCE for signs and symptoms of diabetic foot infection (including osteomyelitis), new pain or tenderness, sores or ulcers involving the lower limbs, and institute appropriate treatment. 5.6 Hypersensitivity Reactions There have been postmarketing reports of serious hypersensitivity reactions (e.g., angioedema) in patients treated with JARDIANCE. If a hypersensitivity reaction occurs, discontinue JARDIANCE; treat promptly per standard of care, and monitor until signs and symptoms resolve. JARDIANCE is contraindicated in patients with hypersensitivity to empagliflozin or any of the excipients in JARDIANCE [see Contraindications (4) ] .

6 ADVERSE REACTIONS The following important adverse reactions are described below and elsewhere in the labeling: • Diabetic Ketoacidosis in Patients with Type 1 Diabetes Mellitus and Other Ketoacidosis [see Warnings and Precautions (5.1) ] • Volume Depletion [see Warnings and Precautions (5.2) ] • Genitourinary Infections, including Urosepsis, Pyelonephritis, Necrotizing Fasciitis of the Perineum (Fournier's Gangrene), and Genital Mycotic Infections [see Warnings and Precautions (5.3) ] • Hypoglycemia [see Warnings and Precautions (5.4) ] • Hypersensitivity Reactions [see Warnings and Precautions (5.6) ] Most common adverse reactions (5% or greater incidence) were urinary tract infections and female genital mycotic infections ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Boehringer Ingelheim Pharmaceuticals, Inc. at 1-800-542-6257 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. JARDIANCE has been evaluated in clinical trials in adult and pediatric patients aged 10 to 17 years with type 2 diabetes mellitus, in adults with heart failure, and in adults with chronic kidney disease. The overall safety profile of JARDIANCE was generally consistent across the studied indications. Clinical Trials in Adults with Type 2 Diabetes Mellitus The data in Table 2 are derived from a pool of four 24-week placebo-controlled trials and 18-week data from a placebo-controlled trial with insulin in adult patients with type 2 diabetes mellitus. JARDIANCE was used as monotherapy in one trial and as add-on therapy in four trials [see Clinical Studies (14.1) ] . These data reflect exposure of 1,976 adult patients to JARDIANCE with a mean exposure duration of approximately 23 weeks. Patients received placebo (N=995), JARDIANCE 10 mg (N=999), or JARDIANCE 25 mg (N=977) once daily. The mean age of the population was 56 years and 3% were older than 75 years of age. More than half (55%) of the population was male; 46% were White, 50% were Asian, and 3% were Black or African American. At baseline, 57% of the population had diabetes mellitus more than 5 years and had a mean hemoglobin A1c (HbA1c) of 8%. Established microvascular complications of diabetes mellitus at baseline included diabetic nephropathy (7%), retinopathy (8%), or neuropathy (16%). Baseline renal function was normal or mildly impaired in 91% of patients and moderately impaired in 9% of patients (mean eGFR 86.8 mL/min/1.73 m 2 ). Table 2 shows adverse reactions (excluding hypoglycemia) that were not present at baseline, occurred more commonly in JARDIANCE-treated patients than on placebo and occurred in greater than or equal to 2% JARDIANCE-treated patients.

f patients and moderately impaired in 9% of patients (mean eGFR 86.8 mL/min/1.73 m 2 ). Table 2 shows adverse reactions (excluding hypoglycemia) that were not present at baseline, occurred more commonly in JARDIANCE-treated patients than on placebo and occurred in greater than or equal to 2% JARDIANCE-treated patients. Table 2Adverse Reactions Reported in ≥2% of Adults with Type 2 Diabetes Mellitus Treated with JARDIANCE and Greater than Placebo in Pooled Placebo-Controlled Clinical Trials of JARDIANCE Monotherapy or Combination Therapy Adverse Reactions Placebo (%) N=995 JARDIANCE 10 mg (%) N=999 JARDIANCE 25 mg (%) N=977 a Predefined adverse event grouping, including, but not limited to, urinary tract infection, asymptomatic bacteriuria, cystitis b Female genital mycotic infections include the following adverse reactions: vulvovaginal mycotic infection, vaginal infection, vulvitis, vulvovaginal candidiasis, genital infection, genital candidiasis, genital infection fungal, genitourinary tract infection, vulvovaginitis, cervicitis, urogenital infection fungal, vaginitis bacterial. Percentages calculated with the number of female subjects in each group as denominator: placebo (N=481), JARDIANCE 10 mg (N=443), JARDIANCE 25 mg (N=420). c Predefined adverse event grouping, including, but not limited to, polyuria, pollakiuria, and nocturia d Male genital mycotic infections include the following adverse reactions: balanoposthitis, balanitis, genital infections fungal, genitourinary tract infection, balanitis candida, scrotal abscess, penile infection. Percentages calculated with the number of male subjects in each group as denominator: placebo (N=514), JARDIANCE 10 mg (N=556), JARDIANCE 25 mg (N=557). Urinary tract infection a 7.6 9.3 7.6 Female genital mycotic infections b 1.5 5.4 6.4 Upper respiratory tract infection 3.8 3.1 4.0 Increased urination c 1.0 3.4 3.2 Dyslipidemia 3.4 3.9 2.9 Arthralgia 2.2 2.4 2.3 Male genital mycotic infections d 0.4 3.1 1.6 Nausea 1.4 2.3 1.1 Thirst (including polydipsia) was reported in 0%, 1.7%, and 1.5% for placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Volume Depletion JARDIANCE causes an osmotic diuresis, which may lead to intravascular volume contraction and adverse reactions related to volume depletion. In the pool of five placebo-controlled clinical trials in adults, adverse reactions related to volume depletion (e.g., blood pressure (ambulatory) decreased, blood pressure systolic decreased, dehydration, hypotension, hypovolemia, orthostatic hypotension, and syncope) were reported by 0.3%, 0.5%, and 0.3% of patients treated with placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. JARDIANCE may increase the risk of hypotension in patients at risk for volume contraction [see Use in Specific Populations (8.5 , 8.6) ]. Increased Urination In the pool of five placebo-controlled clinical trials in adults, adverse reactions of increased urination (e.g., polyuria, pollakiuria, and nocturia) occurred more frequently on JARDIANCE than on placebo (see Table 2 ). Specifically, nocturia was reported by 0.4%, 0.3%, and 0.8% of patients treated with placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Hypoglycemia in Clinical Trials for Glycemic Control in Adults with Type 2 Diabetes Mellitus The incidence of hypoglycemia in adults by trial is shown in Table 3 . The incidence of hypoglycemia increased when JARDIANCE was administered with insulin or sulfonylurea.

o, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Hypoglycemia in Clinical Trials for Glycemic Control in Adults with Type 2 Diabetes Mellitus The incidence of hypoglycemia in adults by trial is shown in Table 3 . The incidence of hypoglycemia increased when JARDIANCE was administered with insulin or sulfonylurea. Table 3Incidence of Overall a and Severe b Hypoglycemic Events in Placebo-Controlled Clinical Trials for Glycemic Control in Adults with Type 2 Diabetes Mellitus c a Overall hypoglycemic events: plasma or capillary glucose of less than or equal to 70 mg/dL b Severe hypoglycemic events: requiring assistance regardless of blood glucose c Treated set (patients who had received at least one dosage of trial drug) d Insulin dosage could not be adjusted during the initial 18-week treatment period Monotherapy (24 weeks) Placebo (n=229) JARDIANCE 10 mg (n=224) JARDIANCE 25 mg (n=223) Overall (%) 0.4 0.4 0.4 Severe (%) 0 0 0 In Combination with Metformin (24 weeks) Placebo + Metformin (n=206) JARDIANCE 10 mg + Metformin (n=217) JARDIANCE 25 mg + Metformin (n=214) Overall (%) 0.5 1.8 1.4 Severe (%) 0 0 0 In Combination with Metformin + Sulfonylurea (24 weeks) Placebo (n=225) JARDIANCE 10 mg + Metformin + Sulfonylurea (n=224) JARDIANCE 25 mg + Metformin + Sulfonylurea (n=217) Overall (%) 8.4 16.1 11.5 Severe (%) 0 0 0 In Combination with Pioglitazone +/- Metformin (24 weeks) Placebo (n=165) JARDIANCE 10 mg + Pioglitazone +/- Metformin (n=165) JARDIANCE 25 mg + Pioglitazone +/- Metformin (n=168) Overall (%) 1.8 1.2 2.4 Severe (%) 0 0 0 In Combination with Basal Insulin +/- Metformin (18 weeks d ) Placebo (n=170) JARDIANCE 10 mg (n=169) JARDIANCE 25 mg (n=155) Overall (%) 20.6 19.5 28.4 Severe (%) 0 0 1.3 In Combination with MDI Insulin +/-Metformin (18 weeks d ) Placebo (n=188) JARDIANCE 10 mg (n=186) JARDIANCE 25 mg (n=189) Overall (%) 37.2 39.8 41.3 Severe (%) 0.5 0.5 0.5 Other Adverse Reactions in Clinical Trials for Glycemic Control in Adults with Type 2 Diabetes Mellitus • Genital Mycotic Infections : In the pool of five placebo-controlled clinical trials in adults, the incidence of genital mycotic infections (e.g., vaginal mycotic infection, vaginal infection, genital infection fungal, vulvovaginal candidiasis, and vulvitis) was increased in patients treated with JARDIANCE compared to placebo, occurring in 0.9%, 4.1%, and 3.7% of patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Discontinuation from trial due to genital infection occurred in 0% of placebo-treated patients and 0.2% of patients treated with either JARDIANCE 10 mg or 25 mg. Genital mycotic infections occurred more frequently in female than male patients (see Table 2 ). Phimosis occurred more frequently in male patients treated with JARDIANCE 10 mg (less than 0.1%) and JARDIANCE 25 mg (0.1%) than placebo (0%). • Urinary Tract Infections : In the pool of five placebo-controlled clinical trials in adults, the incidence of urinary tract infections (e.g., urinary tract infection, asymptomatic bacteriuria, and cystitis) was increased in patients treated with JARDIANCE compared to placebo (see Table 2 ). Patients with a history of chronic or recurrent urinary tract infections were more likely to experience a urinary tract infection. The rate of treatment discontinuation due to urinary tract infections was 0.1%, 0.2%, and 0.1% for placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Urinary tract infections occurred more frequently in female patients. The incidence of urinary tract infections in female patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg was 16.6%, 18.4%, and 17.0%, respectively.

0.1%, 0.2%, and 0.1% for placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Urinary tract infections occurred more frequently in female patients. The incidence of urinary tract infections in female patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg was 16.6%, 18.4%, and 17.0%, respectively. The incidence of urinary tract infections in male patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg was 3.2%, 3.6%, and 4.1%, respectively [see Use in Specific Populations (8.5) ] . Clinical Trial in Pediatric Patients Aged 10 to 17 Years with Type 2 Diabetes Mellitus JARDIANCE was administered to 52 patients in a trial of 157 pediatric patients aged 10 to 17 years with type 2 diabetes mellitus with a mean exposure to JARDIANCE of 23.8 weeks [see Clinical Studies (14.2) ] . Background therapies as adjunct to diet and exercise included metformin (51%), a combination of metformin and insulin (40.1%), insulin (3.2%), or none (5.7%). The mean HbA1c at baseline was 8.0% and the mean duration of type 2 diabetes mellitus was 2.1 years. The mean age was 14.5 years (range: 10-17 years) and 51.6% were aged 15 years and older. Approximately, 50% were White, 6% were Asian, 31% were Black or African American, and 38% were of Hispanic or Latino ethnicity. The mean BMI was 36.0 kg/m 2 and mean BMI Z-score was 3.0. Approximately 25% of the trial population had microalbuminuria or macroalbuminuria. The risk of hypoglycemia was higher in pediatric patients treated with JARDIANCE regardless of concomitant insulin use. Hypoglycemia, defined as a blood glucose <54 mg/dL, occurred in 10 (19.2%) patients and in 4 (7.5%) patients treated with JARDIANCE and placebo, respectively. No severe hypoglycemic events occurred (severe hypoglycemia was defined as an event requiring the assistance of another person to actively administer carbohydrates, glucagon or take other corrective actions). Clinical Trials in Adults with Heart Failure No new adverse reactions were identified in EMPEROR-Reduced or EMPEROR-Preserved heart failure trials. Clinical Trial in Adults with Chronic Kidney Disease The safety profile in patients with chronic kidney disease was generally consistent with that observed across the studied indications. In a long-term cardio-renal outcome trial [see Clinical Studies 14.5 ] , in patients with chronic kidney disease, the occurrence of lower limb amputations was reported with event rates of 2.9, and 4.3 events per 1,000 patient-years in the placebo, and JARDIANCE 10 mg treatment arms, respectively [see Warnings and Precautions (5.5) ]. Laboratory Test Abnormalities in Clinical Trials Increases in Serum Creatinine and Decreases in eGFR Initiation of JARDIANCE causes an increase in serum creatinine and decrease in eGFR within weeks of starting therapy and then these changes stabilize. In a trial of adults with moderate renal impairment, larger mean changes were observed. In a long-term cardiovascular outcomes trial, the increase in serum creatinine and decrease in eGFR generally did not exceed 0.1 mg/dL and -9.0 mL/min/1.73 m 2 , respectively, at Week 4, and reversed after treatment discontinuation, suggesting acute hemodynamic changes may play a role in the renal function changes observed with JARDIANCE. Increase in Low-Density Lipoprotein Cholesterol (LDL-C) Dose-related increases in low-density lipoprotein cholesterol (LDL-C) were observed in adults treated with JARDIANCE. LDL-C increased by 2.3%, 4.6%, and 6.5% in patients treated with placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. The range of mean baseline LDL-C levels was 90.3 to 90.6 mg/dL across treatment groups.

d increases in low-density lipoprotein cholesterol (LDL-C) were observed in adults treated with JARDIANCE. LDL-C increased by 2.3%, 4.6%, and 6.5% in patients treated with placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. The range of mean baseline LDL-C levels was 90.3 to 90.6 mg/dL across treatment groups. Increase in Hematocrit In a pool of four placebo-controlled trials in adults, median hematocrit decreased by 1.3% in placebo and increased by 2.8% in JARDIANCE 10 mg and 2.8% in JARDIANCE 25 mg treated patients. At the end of treatment, 0.6%, 2.7%, and 3.5% of patients with hematocrits initially within the reference range had values above the upper limit of the reference range with placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. 6.2 Postmarketing Experience Additional adverse reactions have been identified during postapproval use of JARDIANCE. Because these reactions are reported voluntarily from a population of uncertain size, it is generally not possible to reliably estimate their frequency or establish a causal relationship to drug exposure. Gastrointestinal Disorders: Constipation Infections: Necrotizing fasciitis of the perineum (Fournier's gangrene), urosepsis and pyelonephritis Metabolism and Nutrition Disorders: Ketoacidosis Renal and Urinary Disorders: Acute kidney injury Skin and Subcutaneous Tissue Disorders: Angioedema, skin reactions (e.g., rash, urticaria)

<table ID="_Reftable2" width="75%"><caption>Table 2Adverse Reactions Reported in &#x2265;2% of Adults with Type 2 Diabetes Mellitus Treated with JARDIANCE and Greater than Placebo in Pooled Placebo-Controlled Clinical Trials of JARDIANCE Monotherapy or Combination Therapy</caption><col width="28%"/><col width="18%"/><col width="20%"/><col width="20%"/><thead><tr><th align="center" styleCode="Rrule Botrule Lrule Toprule " valign="top"><content styleCode="bold">Adverse Reactions</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">Placebo (%)</content> <content styleCode="bold">N=995</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE 10 mg (%)</content> <content styleCode="bold">N=999</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE 25 mg (%)</content> <content styleCode="bold">N=977</content></th></tr></thead><tfoot><tr><td align="left" colspan="4" valign="top">^aPredefined adverse event grouping, including, but not limited to, urinary tract infection, asymptomatic bacteriuria, cystitis ^bFemale genital mycotic infections include the following adverse reactions: vulvovaginal mycotic infection, vaginal infection, vulvitis, vulvovaginal candidiasis, genital infection, genital candidiasis, genital infection fungal, genitourinary tract infection, vulvovaginitis, cervicitis, urogenital infection fungal, vaginitis bacterial. Percentages calculated with the number of female subjects in each group as denominator: placebo (N=481), JARDIANCE 10 mg (N=443), JARDIANCE 25 mg (N=420). ^cPredefined adverse event grouping, including, but not limited to, polyuria, pollakiuria, and nocturia ^dMale genital mycotic infections include the following adverse reactions: balanoposthitis, balanitis, genital infections fungal, genitourinary tract infection, balanitis candida, scrotal abscess, penile infection.

ined adverse event grouping, including, but not limited to, polyuria, pollakiuria, and nocturia ^dMale genital mycotic infections include the following adverse reactions: balanoposthitis, balanitis, genital infections fungal, genitourinary tract infection, balanitis candida, scrotal abscess, penile infection. Percentages calculated with the number of male subjects in each group as denominator: placebo (N=514), JARDIANCE 10 mg (N=556), JARDIANCE 25 mg (N=557).</td></tr></tfoot><tbody><tr><td styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph>Urinary tract infection^a</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="top"><paragraph>7.6</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="top"><paragraph>9.3</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="top"><paragraph>7.6</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Female genital mycotic infections^b</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.5</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>5.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>6.4</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Upper respiratory tract infection</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>3.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>3.1</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>4.0</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Increased urination^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>3.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>3.2</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Dyslipidemia</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>3.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>3.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>2.9</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Arthralgia</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>2.2</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>2.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>2.3</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Male genital mycotic infections^d</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>3.1</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.6</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph>Nausea</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>2.3</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.1</paragraph></td></tr></tbody></table>

graph>Nausea</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>2.3</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.1</paragraph></td></tr></tbody></table> <table ID="_Reftable3" width="75%"><caption>Table 3Incidence of Overall^a and Severe^b Hypoglycemic Events in Placebo-Controlled Clinical Trials for Glycemic Control in Adults with Type 2 Diabetes Mellitus^c</caption><col width="25%"/><col width="18%"/><col width="22%"/><col width="22%"/><tfoot><tr><td align="left" colspan="4" valign="top">^aOverall hypoglycemic events: plasma or capillary glucose of less than or equal to 70 mg/dL ^bSevere hypoglycemic events: requiring assistance regardless of blood glucose ^cTreated set (patients who had received at least one dosage of trial drug) ^dInsulin dosage could not be adjusted during the initial 18-week treatment period</td></tr></tfoot><tbody><tr><td styleCode="Rrule Botrule Lrule Toprule " valign="top"><paragraph><content styleCode="bold">Monotherapy (24 weeks)</content></paragraph></td><td align="center" styleCode="Rrule Botrule Toprule " valign="top"><paragraph><content styleCode="bold">Placebo </content> <content styleCode="bold">(n=229)</content></paragraph></td><td align="center" styleCode="Rrule Botrule Toprule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 10 mg (n=224)</content></paragraph></td><td align="center" styleCode="Rrule Botrule Toprule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 25 mg (n=223)</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Overall (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.4</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Severe (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">In Combination with Metformin (24 weeks)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">Placebo + Metformin </content> <content styleCode="bold">(n=206)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 10 mg + Metformin </content> <content styleCode="bold">(n=217)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 25 mg + Metformin </content> <content styleCode="bold">(n=214)</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Overall (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.5</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.4</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Severe (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0<

e="Rrule Botrule " valign="top"><paragraph>1.4</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Severe (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0< /paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">In Combination with Metformin + Sulfonylurea </content> <content styleCode="bold">(24 weeks)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">Placebo (n=225)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 10 mg + Metformin + Sulfonylurea (n=224)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 25 mg + Metformin + Sulfonylurea (n=217)</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Overall (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>16.1</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>11.5</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Severe (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">In Combination with Pioglitazone +/- Metformin </content> <content styleCode="bold">(24 weeks)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">Placebo (n=165)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 10 mg + Pioglitazone +/- Metformin </content> <content styleCode="bold">(n=165)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 25 mg + Pioglitazone +/- Metformin </content> <content styleCode="bold"> (n=168)</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Overall (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.2</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>2.4</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Severe (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">In Combination with Basal Insulin +/- Metformin </content> <content styleCode="bold">(18 weeks^d)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">Placebo (n=170)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode=

formin </content> <content styleCode="bold">(18 weeks^d)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">Placebo (n=170)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode= "bold">JARDIANCE 10 mg </content> <content styleCode="bold">(n=169)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 25 mg </content> <content styleCode="bold">(n=155)</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Overall (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>20.6</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>19.5</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>28.4</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Severe (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>1.3</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">In Combination with MDI Insulin +/-Metformin </content> <content styleCode="bold">(18 weeks^d)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">Placebo (n=188)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 10 mg </content> <content styleCode="bold">(n=186)</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph><content styleCode="bold">JARDIANCE 25 mg </content> <content styleCode="bold">(n=189)</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Overall (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>37.2</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>39.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>41.3</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph>Severe (%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.5</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.5</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.5</paragraph></td></tr></tbody></table>

7 DRUG INTERACTIONS See Table 4 for clinically relevant interactions with JARDIANCE. Table 4Clinically Relevant Interactions with JARDIANCE Diuretics Clinical Impact Coadministration of empagliflozin with diuretics resulted in increased urine volume and frequency of voids, which might enhance the potential for volume depletion. Intervention Before initiating JARDIANCE, assess volume status and renal function. In patients with volume depletion, correct this condition before initiating JARDIANCE. Monitor for signs and symptoms of volume depletion, and renal function after initiating therapy. Insulin or Insulin Secretagogues Clinical Impact The risk of hypoglycemia is increased when JARDIANCE is used in combination with insulin secretagogues (e.g., sulfonylurea) or insulin. Intervention Coadministration of JARDIANCE with an insulin secretagogue (e.g., sulfonylurea) or insulin may require lower dosages of the insulin secretagogue or insulin to reduce the risk of hypoglycemia. Lithium Clinical Impact Concomitant use of an SGLT2 inhibitor with lithium may decrease serum lithium concentrations. Intervention Monitor serum lithium concentration more frequently during JARDIANCE initiation and dosage changes. Positive Urine Glucose Test Clinical Impact SGLT2 inhibitors increase urinary glucose excretion and will lead to positive urine glucose tests. Intervention Monitoring glycemic control with urine glucose tests is not recommended in patients taking SGLT2 inhibitors. Use alternative methods to monitor glycemic control. Interference with 1,5-anhydroglucitol (1,5-AG) Assay Clinical Impact Measurements of 1,5-AG are unreliable in assessing glycemic control in patients taking SGLT2 inhibitors. Intervention Monitoring glycemic control with 1,5-AG assay is not recommended. Use alternative methods to monitor glycemic control. See full prescribing information for information on drug interactions and interference of JARDIANCE with laboratory tests. ( 7 )

<table ID="_Reftable4" width="75%"><caption>Table 4Clinically Relevant Interactions with JARDIANCE</caption><col width="23%"/><col width="64%"/><thead><tr><th align="left" colspan="2" styleCode="Rrule Botrule Lrule Toprule " valign="top"><content styleCode="bold">Diuretics</content></th></tr></thead><tbody><tr><td styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="italics">Clinical Impact</content></paragraph></td><td styleCode="Rrule Toprule Botrule " valign="top"><paragraph>Coadministration of empagliflozin with diuretics resulted in increased urine volume and frequency of voids, which might enhance the potential for volume depletion.</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="italics">Intervention</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>Before initiating JARDIANCE, assess volume status and renal function. In patients with volume depletion, correct this condition before initiating JARDIANCE.

Lrule Botrule " valign="top"><paragraph><content styleCode="italics">Intervention</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>Before initiating JARDIANCE, assess volume status and renal function. In patients with volume depletion, correct this condition before initiating JARDIANCE. Monitor for signs and symptoms of volume depletion, and renal function after initiating therapy.</paragraph></td></tr><tr><td colspan="2" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">Insulin or Insulin Secretagogues</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="italics">Clinical Impact</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>The risk of hypoglycemia is increased when JARDIANCE is used in combination with insulin secretagogues (e.g., sulfonylurea) or insulin.</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="italics">Intervention</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>Coadministration of JARDIANCE with an insulin secretagogue (e.g., sulfonylurea) or insulin may require lower dosages of the insulin secretagogue or insulin to reduce the risk of hypoglycemia.</paragraph></td></tr><tr><td colspan="2" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">Lithium</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="italics">Clinical Impact</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>Concomitant use of an SGLT2 inhibitor with lithium may decrease serum lithium concentrations.</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="italics">Intervention</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>Monitor serum lithium concentration more frequently during JARDIANCE initiation and dosage changes.</paragraph></td></tr><tr><td colspan="2" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">Positive Urine Glucose Test</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="italics">Clinical Impact</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>SGLT2 inhibitors increase urinary glucose excretion and will lead to positive urine glucose tests.</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="italics">Intervention</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>Monitoring glycemic control with urine glucose tests is not recommended in patients taking SGLT2 inhibitors. Use alternative methods to monitor glycemic control.</paragraph></td></tr><tr><td colspan="2" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">Interference with 1,5-anhydroglucitol (1,5-AG) Assay</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="italics">Clinical Impact</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>Measurements of 1,5-AG are unreliable in assessing glycemic control in patients taking SGLT2 inhibitors.</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph><content styleCode="italics">Intervention</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"><paragraph>Monitoring glycemic control with 1,5-AG assay is not recommended. Use alternative methods to monitor glycemic control.</paragraph></td></tr></tbody></table>

8 USE IN SPECIFIC POPULATIONS • Pregnancy: Advise females of the potential risk to a fetus especially during the second and third trimesters. ( 8.1 ) • Lactation: Not recommended when breastfeeding. ( 8.2 ) • Geriatric Patients: Higher incidence of adverse reactions related to volume depletion and reduced renal function. ( 8.5 ) • Renal Impairment: Higher incidence of adverse reactions related to reduced renal function. ( 8.6 ) 8.1 Pregnancy Risk Summary Based on animal data showing adverse renal effects, JARDIANCE is not recommended during the second and third trimesters of pregnancy. The limited available data with JARDIANCE in pregnant women are not sufficient to determine a drug-associated risk for major birth defects and miscarriage. There are risks to the mother and fetus associated with poorly controlled diabetes in pregnancy [see Clinical Considerations ] . In animal studies, adverse renal changes were observed in rats when empagliflozin was administered during a period of renal development corresponding to the late second and third trimesters of human pregnancy. Doses approximately 13-times the maximum clinical dose caused renal pelvic and tubule dilatations that were reversible [see Data ] . The estimated background risk of major birth defects is 6% to 10% in women with pre-gestational diabetes with a HbA1c >7 and has been reported to be as high as 20% to 25% in women with HbA1c >10. The estimated background risk of miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. Clinical Considerations Disease-associated maternal and/or embryo/fetal risk Poorly controlled diabetes in pregnancy increases the maternal risk for diabetic ketoacidosis, pre-eclampsia, spontaneous abortions, preterm delivery, and delivery complications. Poorly controlled diabetes increases the fetal risk for major birth defects, stillbirth, and macrosomia related morbidity. Data Animal Data Empagliflozin dosed directly to juvenile rats from postnatal day (PND) 21 until PND 90 at doses of 1, 10, 30, and 100 mg/kg/day caused increased kidney weights and renal tubular and pelvic dilatation at 100 mg/kg/day, which approximates 13-times the maximum clinical dose of 25 mg, based on AUC. These findings were not observed after a 13-week, drug-free recovery period. These outcomes occurred with drug exposure during periods of renal development in rats that correspond to the late second and third trimester of human renal development. In embryo-fetal development studies in rats and rabbits, empagliflozin was administered for intervals coinciding with the first trimester period of organogenesis in humans. Doses up to 300 mg/kg/day, which approximates 48-times (rats) and 128-times (rabbits) the maximum clinical dose of 25 mg (based on AUC), did not result in adverse developmental effects. In rats, at higher doses of empagliflozin causing maternal toxicity, malformations of limb bones increased in fetuses at 700 mg/kg/day or 154-times the 25 mg maximum clinical dose. Empagliflozin crosses the placenta and reaches fetal tissues in rats. In the rabbit, higher doses of empagliflozin resulted in maternal and fetal toxicity at 700 mg/kg/day, or 139-times the 25 mg maximum clinical dose.

ons of limb bones increased in fetuses at 700 mg/kg/day or 154-times the 25 mg maximum clinical dose. Empagliflozin crosses the placenta and reaches fetal tissues in rats. In the rabbit, higher doses of empagliflozin resulted in maternal and fetal toxicity at 700 mg/kg/day, or 139-times the 25 mg maximum clinical dose. In pre- and postnatal development studies in pregnant rats, empagliflozin was administered from gestation day 6 through to lactation day 20 (weaning) at up to 100 mg/kg/day (approximately 16-times the 25 mg maximum clinical dose) without maternal toxicity. Reduced body weight was observed in the offspring at greater than or equal to 30 mg/kg/day (approximately 4-times the 25 mg maximum clinical dose). 8.2 Lactation Risk Summary There is limited information regarding the presence of JARDIANCE in human milk, the effects of JARDIANCE on the breastfed infant or the effects on milk production. Empagliflozin is present in the milk of lactating rats [see Data ] . Since human kidney maturation occurs in utero and during the first 2 years of life when lactational exposure may occur, there may be risk to the developing human kidney. Because of the potential for serious adverse reactions in a breastfed infant, including the potential for empagliflozin to affect postnatal renal development, advise patients that use of JARDIANCE is not recommended while breastfeeding. Data Empagliflozin was present at a low level in rat fetal tissues after a single oral dose to the dams at gestation day 18. In rat milk, the mean milk to plasma ratio ranged from 0.634 to 5, and was greater than one from 2 to 24 hours post-dose. The mean maximal milk to plasma ratio of 5 occurred at 8 hours post-dose, suggesting accumulation of empagliflozin in the milk. Juvenile rats directly exposed to empagliflozin showed a risk to the developing kidney (renal pelvic and tubular dilatations) during maturation. 8.4 Pediatric Use The safety and effectiveness of JARDIANCE as an adjunct to diet and exercise to improve glycemic control in type 2 diabetes mellitus have been established in pediatric patients aged 10 years and older. Use of JARDIANCE for this indication is supported by evidence from a 26-week double-blind, placebo-controlled clinical trial, with a double-blind active treatment safety extension period of up to 52 weeks in 157 pediatric patients aged 10 to 17 years with type 2 diabetes mellitus and a pediatric pharmacokinetic study [see Clinical Pharmacology (12.3) and Clinical Studies (14.2) ] . The safety profile of pediatric patients treated with JARDIANCE was similar to that observed in adults with type 2 diabetes mellitus, with the exception of hypoglycemia risk which was higher in pediatric patients treated with JARDIANCE regardless of concomitant insulin use [see Warnings and Precautions (5.4) and Adverse Reactions (6.1) ]. The safety and effectiveness of JARDIANCE have not been established in pediatric patients less than 10 years of age as an adjunct to diet and exercise to improve glycemic control in type 2 diabetes mellitus. The safety and effectiveness of JARDIANCE have not been established in pediatric patients to reduce the risk of: • cardiovascular death and hospitalization for heart failure in patients with heart failure. • sustained decline in eGFR, end-stage kidney disease, cardiovascular death, and hospitalization in patients with chronic kidney disease at risk of progression. • cardiovascular death in patients with type 2 diabetes mellitus and established cardiovascular disease. 8.5 Geriatric Use In glycemic control trials in patients with type 2 diabetes mellitus, a total of 2,721 (32%) patients treated with JARDIANCE were 65 years of age and older, and 491 (6%) were 75 years of age and older.

rdiovascular death in patients with type 2 diabetes mellitus and established cardiovascular disease. 8.5 Geriatric Use In glycemic control trials in patients with type 2 diabetes mellitus, a total of 2,721 (32%) patients treated with JARDIANCE were 65 years of age and older, and 491 (6%) were 75 years of age and older. JARDIANCE is expected to have diminished glycemic efficacy in elderly patients with renal impairment [see Use in Specific Populations (8.6) ] . The risk of volume depletion-related adverse reactions increased in patients who were 75 years of age and older to 2.1%, 2.3%, and 4.4% for placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg. The risk of urinary tract infections increased in patients who were 75 years of age and older to 10.5%, 15.7%, and 15.1% in patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively [see Warnings and Precautions (5.2) and Adverse Reactions (6.1) ] . In the EMPEROR-Reduced, EMPEROR-Preserved, and EMPA-KIDNEY trials, no overall differences in safety and effectiveness have been observed between patients 65 years of age and older and younger adult patients. EMPEROR-Reduced included 1,188 (64%) patients treated with JARDIANCE 65 years of age and older, and 503 (27%) patients 75 years of age and older. EMPEROR-Preserved included 2,403 (80%) patients treated with JARDIANCE 65 years of age and older, and 1,281 (43%) patients 75 years of age and older. EMPA-KIDNEY included 1,803 (55%) patients treated with JARDIANCE 65 years of age and older, and 758 (23%) patients 75 years of age and older. 8.6 Renal Impairment The efficacy and safety of JARDIANCE for glycemic control were evaluated in a trial of adult patients with type 2 diabetes mellitus with mild and moderate renal impairment (eGFR 30 to less than 90 mL/min/1.73 m 2 ) [see Clinical Studies (14.1) ] . In this trial, 195 adult patients exposed to JARDIANCE had an eGFR between 60 and 90 mL/min/1.73 m 2 , 91 adult patients exposed to JARDIANCE had an eGFR between 45 and 60 mL/min/1.73 m 2 , and 97 patients exposed to JARDIANCE had an eGFR between 30 and 45 mL/min/1.73 m 2 . The glucose lowering benefit of JARDIANCE 25 mg decreased in adult patients with worsening renal function. The risks of renal impairment, volume depletion adverse reactions and urinary tract infection-related adverse reactions increased with worsening renal function [see Warnings and Precautions (5.2) ] . Use of JARDIANCE for glycemic control in patients without established cardiovascular disease or cardiovascular risk factors is not recommended when eGFR is less than 30 mL/min/1.73 m 2 . JARDIANCE was evaluated in 7,020 adult patients with type 2 diabetes and established cardiovascular disease (eGFR greater than or equal to 30 mL/min/1.73 m 2 ) in the EMPA-REG OUTCOME trial, in a total of 9,718 patients with heart failure (eGFR greater than or equal to 20 mL/min/1.73 m 2 ) in the EMPEROR-Reduced and EMPEROR-Preserved trials, and in 6,609 adult patients with chronic kidney disease (eGFR 20 to 90 mL/min/1.73 m 2 ) in the EMPA-KIDNEY study. The safety profile across eGFR subgroups in these trials was consistent with the known safety profile [see Adverse Reactions (6.1) and Clinical Studies (14.3 , 14.4 , 14.5) ]. Efficacy and safety trials with JARDIANCE did not enroll adult patients with an eGFR less than 20 mL/min/1.73 m 2 or on dialysis. Once enrolled, adult patients in the EMPA-REG OUTCOME, EMPEROR-Reduced, EMPEROR-Preserved, and EMPA-KIDNEY trials were not required to discontinue therapy for worsening of eGFR to less than 20 mL/min/1.73 m 2 or initiation of dialysis [see Clinical Studies (14.3 , 14.4 , 14.5) ]. 8.7 Hepatic Impairment JARDIANCE may be used in patients with hepatic impairment [see Clinical Pharmacology (12.3) ] .

8.1 Pregnancy Risk Summary Based on animal data showing adverse renal effects, JARDIANCE is not recommended during the second and third trimesters of pregnancy. The limited available data with JARDIANCE in pregnant women are not sufficient to determine a drug-associated risk for major birth defects and miscarriage. There are risks to the mother and fetus associated with poorly controlled diabetes in pregnancy [see Clinical Considerations ] . In animal studies, adverse renal changes were observed in rats when empagliflozin was administered during a period of renal development corresponding to the late second and third trimesters of human pregnancy. Doses approximately 13-times the maximum clinical dose caused renal pelvic and tubule dilatations that were reversible [see Data ] . The estimated background risk of major birth defects is 6% to 10% in women with pre-gestational diabetes with a HbA1c >7 and has been reported to be as high as 20% to 25% in women with HbA1c >10. The estimated background risk of miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. Clinical Considerations Disease-associated maternal and/or embryo/fetal risk Poorly controlled diabetes in pregnancy increases the maternal risk for diabetic ketoacidosis, pre-eclampsia, spontaneous abortions, preterm delivery, and delivery complications. Poorly controlled diabetes increases the fetal risk for major birth defects, stillbirth, and macrosomia related morbidity. Data Animal Data Empagliflozin dosed directly to juvenile rats from postnatal day (PND) 21 until PND 90 at doses of 1, 10, 30, and 100 mg/kg/day caused increased kidney weights and renal tubular and pelvic dilatation at 100 mg/kg/day, which approximates 13-times the maximum clinical dose of 25 mg, based on AUC. These findings were not observed after a 13-week, drug-free recovery period. These outcomes occurred with drug exposure during periods of renal development in rats that correspond to the late second and third trimester of human renal development. In embryo-fetal development studies in rats and rabbits, empagliflozin was administered for intervals coinciding with the first trimester period of organogenesis in humans. Doses up to 300 mg/kg/day, which approximates 48-times (rats) and 128-times (rabbits) the maximum clinical dose of 25 mg (based on AUC), did not result in adverse developmental effects. In rats, at higher doses of empagliflozin causing maternal toxicity, malformations of limb bones increased in fetuses at 700 mg/kg/day or 154-times the 25 mg maximum clinical dose. Empagliflozin crosses the placenta and reaches fetal tissues in rats. In the rabbit, higher doses of empagliflozin resulted in maternal and fetal toxicity at 700 mg/kg/day, or 139-times the 25 mg maximum clinical dose. In pre- and postnatal development studies in pregnant rats, empagliflozin was administered from gestation day 6 through to lactation day 20 (weaning) at up to 100 mg/kg/day (approximately 16-times the 25 mg maximum clinical dose) without maternal toxicity. Reduced body weight was observed in the offspring at greater than or equal to 30 mg/kg/day (approximately 4-times the 25 mg maximum clinical dose).

8.4 Pediatric Use The safety and effectiveness of JARDIANCE as an adjunct to diet and exercise to improve glycemic control in type 2 diabetes mellitus have been established in pediatric patients aged 10 years and older. Use of JARDIANCE for this indication is supported by evidence from a 26-week double-blind, placebo-controlled clinical trial, with a double-blind active treatment safety extension period of up to 52 weeks in 157 pediatric patients aged 10 to 17 years with type 2 diabetes mellitus and a pediatric pharmacokinetic study [see Clinical Pharmacology (12.3) and Clinical Studies (14.2) ] . The safety profile of pediatric patients treated with JARDIANCE was similar to that observed in adults with type 2 diabetes mellitus, with the exception of hypoglycemia risk which was higher in pediatric patients treated with JARDIANCE regardless of concomitant insulin use [see Warnings and Precautions (5.4) and Adverse Reactions (6.1) ]. The safety and effectiveness of JARDIANCE have not been established in pediatric patients less than 10 years of age as an adjunct to diet and exercise to improve glycemic control in type 2 diabetes mellitus. The safety and effectiveness of JARDIANCE have not been established in pediatric patients to reduce the risk of: • cardiovascular death and hospitalization for heart failure in patients with heart failure. • sustained decline in eGFR, end-stage kidney disease, cardiovascular death, and hospitalization in patients with chronic kidney disease at risk of progression. • cardiovascular death in patients with type 2 diabetes mellitus and established cardiovascular disease.

8.5 Geriatric Use In glycemic control trials in patients with type 2 diabetes mellitus, a total of 2,721 (32%) patients treated with JARDIANCE were 65 years of age and older, and 491 (6%) were 75 years of age and older. JARDIANCE is expected to have diminished glycemic efficacy in elderly patients with renal impairment [see Use in Specific Populations (8.6) ] . The risk of volume depletion-related adverse reactions increased in patients who were 75 years of age and older to 2.1%, 2.3%, and 4.4% for placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg. The risk of urinary tract infections increased in patients who were 75 years of age and older to 10.5%, 15.7%, and 15.1% in patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively [see Warnings and Precautions (5.2) and Adverse Reactions (6.1) ] . In the EMPEROR-Reduced, EMPEROR-Preserved, and EMPA-KIDNEY trials, no overall differences in safety and effectiveness have been observed between patients 65 years of age and older and younger adult patients. EMPEROR-Reduced included 1,188 (64%) patients treated with JARDIANCE 65 years of age and older, and 503 (27%) patients 75 years of age and older. EMPEROR-Preserved included 2,403 (80%) patients treated with JARDIANCE 65 years of age and older, and 1,281 (43%) patients 75 years of age and older. EMPA-KIDNEY included 1,803 (55%) patients treated with JARDIANCE 65 years of age and older, and 758 (23%) patients 75 years of age and older.

10 OVERDOSAGE In the event of an overdose with JARDIANCE, consider contacting the Poison Help line (1-800-222-1222) or a medical toxicologist for additional overdosage management recommendations. Removal of empagliflozin by hemodialysis has not been studied.

11 DESCRIPTION JARDIANCE tablets for oral use contain empagliflozin, an inhibitor of the SGLT2. The chemical name of empagliflozin is D-Glucitol,1,5-anhydro-1-C-[4-chloro-3-[[4-[[(3S)-tetrahydro-3-furanyl]oxy]phenyl]methyl]phenyl]-, (1S). Its molecular formula is C 23 H 27 ClO 7 and the molecular weight is 450.91. The structural formula is: Empagliflozin is a white to yellowish, non-hygroscopic powder. It is very slightly soluble in water, sparingly soluble in methanol, slightly soluble in ethanol and acetonitrile, soluble in 50% acetonitrile/water, and practically insoluble in toluene. Each film-coated tablet of JARDIANCE contains 10 mg or 25 mg of empagliflozin (free base) and the following inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, hydroxypropyl cellulose, lactose monohydrate, magnesium stearate, and microcrystalline cellulose. In addition, the film coating contains the following inactive ingredients: ferric oxide yellow, hypromellose, polyethylene glycol, talc, and titanium dioxide. Chemical Structure

12 CLINICAL PHARMACOLOGY 12.1 Mechanism of Action Empagliflozin is an inhibitor of SGLT2, the predominant transporter responsible for reabsorption of glucose from the glomerular filtrate back into the circulation. By inhibiting SGLT2, empagliflozin reduces renal reabsorption of filtered glucose and lowers the renal threshold for glucose, and thereby increases urinary glucose excretion. Empagliflozin also reduces sodium reabsorption and increases the delivery of sodium to the distal tubule. This may influence several physiological functions including, but not restricted to, increasing tubuloglomerular feedback and reducing intraglomerular pressure, lowering both pre- and afterload of the heart and downregulating sympathetic activity. 12.2 Pharmacodynamics Urinary Glucose Excretion In patients with type 2 diabetes mellitus, urinary glucose excretion increased immediately following a dose of empagliflozin and was maintained at the end of a 4-week treatment period averaging at approximately 64 grams per day with 10 mg empagliflozin and 78 grams per day with 25 mg empagliflozin once daily [see Clinical Studies (14) ]. Data from single oral doses of empagliflozin in healthy subjects indicate that, on average, the elevation in urinary glucose excretion approaches baseline by about 3 days for the 10 mg and 25 mg doses. Urinary Volume In a 5-day study, mean 24-hour urine volume increase from baseline was 341 mL on Day 1 and 135 mL on Day 5 of empagliflozin 25 mg once daily treatment. Cardiac Electrophysiology In a randomized, placebo-controlled, active-comparator, crossover study, 30 healthy subjects were administered a single oral dose of empagliflozin 25 mg, empagliflozin 200 mg (8 times the maximum dose), moxifloxacin, and placebo. No increase in QTc was observed with either 25 mg or 200 mg empagliflozin. 12.3 Pharmacokinetics The pharmacokinetics of empagliflozin has been characterized in healthy volunteers and patients with type 2 diabetes mellitus and no clinically relevant differences were noted between the two populations. The steady-state mean plasma AUC and C max were 1,870 nmol∙h/L and 259 nmol/L, respectively, with 10 mg empagliflozin once daily treatment, and 4,740 nmol∙h/L and 687 nmol/L, respectively, with 25 mg empagliflozin once daily treatment. Systemic exposure of empagliflozin increased in a dose-proportional manner in the therapeutic dose range. Empagliflozin does not appear to have time-dependent pharmacokinetic characteristics. Following once-daily dosing, up to 22% accumulation, with respect to plasma AUC, was observed at steady-state. Absorption After oral administration, peak plasma concentrations of empagliflozin were reached at 1.5 hours post-dose. Administration of 25 mg empagliflozin after intake of a high-fat and high-calorie meal resulted in slightly lower exposure; AUC decreased by approximately 16% and C max decreased by approximately 37%, compared to fasted condition. The observed effect of food on empagliflozin pharmacokinetics was not considered clinically relevant and empagliflozin may be administered with or without food. Distribution The apparent steady-state volume of distribution was estimated to be 73.8 L based on a population pharmacokinetic analysis. Following administration of an oral [ 14 C]-empagliflozin solution to healthy subjects, the red blood cell partitioning was approximately 36.8% and plasma protein binding was 86.2%.

. Distribution The apparent steady-state volume of distribution was estimated to be 73.8 L based on a population pharmacokinetic analysis. Following administration of an oral [ 14 C]-empagliflozin solution to healthy subjects, the red blood cell partitioning was approximately 36.8% and plasma protein binding was 86.2%. Elimination The apparent terminal elimination half-life of empagliflozin was estimated to be 12.4 h and apparent oral clearance was 10.6 L/h based on the population pharmacokinetic analysis. Metabolism No major metabolites of empagliflozin were detected in human plasma and the most abundant metabolites were three glucuronide conjugates (2-O-, 3-O-, and 6-O-glucuronide). Systemic exposure of each metabolite was less than 10% of total drug-related material. In vitro studies suggested that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT2B7, UGT1A3, UGT1A8, and UGT1A9. Excretion Following administration of an oral [ 14 C]-empagliflozin solution to healthy subjects, approximately 95.6% of the drug-related radioactivity was eliminated in feces (41.2%) or urine (54.4%). The majority of drug-related radioactivity recovered in feces was unchanged parent drug and approximately half of drug-related radioactivity excreted in urine was unchanged parent drug. Specific Populations Pediatric Patients The pharmacokinetics and pharmacodynamics of empagliflozin were investigated in pediatric patients aged 10 to 17 years with type 2 diabetes mellitus. Oral administration of empagliflozin at 10 mg and 25 mg resulted in exposure within the range observed in adult patients. Effects of Age, Body Mass Index, Gender, and Race Age, body mass index (BMI), gender and race (Asians versus primarily Whites) do not have a clinically meaningful effect on pharmacokinetics of empagliflozin. Patients with Hepatic Impairment In adult patients with mild, moderate, and severe hepatic impairment according to the Child-Pugh classification, AUC of empagliflozin increased by approximately 23%, 47%, and 75%, and C max increased by approximately 4%, 23%, and 48%, respectively, compared to subjects with normal hepatic function. Patients with Renal Impairment In adult patients with type 2 diabetes mellitus with mild (eGFR: 60 to less than 90 mL/min/1.73 m 2 ), moderate (eGFR: 30 to less than 60 mL/min/1.73 m 2 ), and severe (eGFR: less than 30 mL/min/1.73 m 2 ) renal impairment and patients on dialysis due to kidney failure, AUC of empagliflozin increased by approximately 18%, 20%, 66%, and 48%, respectively, compared to subjects with normal renal function. Peak plasma levels of empagliflozin were similar in patients with moderate renal impairment and patients on dialysis due to kidney failure compared to subjects with normal renal function. Peak plasma levels of empagliflozin were roughly 20% higher in patients with mild and severe renal impairment as compared to patients with normal renal function. Population pharmacokinetic analysis showed that the apparent oral clearance of empagliflozin decreased, with a decrease in eGFR leading to an increase in drug exposure. However, the fraction of empagliflozin that was excreted unchanged in urine, and urinary glucose excretion, declined with decrease in eGFR. Drug Interaction Studies In vitro Assessment of Drug Interactions Empagliflozin does not inhibit, inactivate, or induce CYP450 isoforms. In vitro data suggest that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT1A3, UGT1A8, UGT1A9, and UGT2B7. Empagliflozin does not inhibit UGT1A1, UGT1A3, UGT1A8, UGT1A9, or UGT2B7.

not inhibit, inactivate, or induce CYP450 isoforms. In vitro data suggest that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT1A3, UGT1A8, UGT1A9, and UGT2B7. Empagliflozin does not inhibit UGT1A1, UGT1A3, UGT1A8, UGT1A9, or UGT2B7. Therefore, no effect of empagliflozin is anticipated on concomitantly administered drugs that are substrates of the major CYP450 isoforms or UGT1A1, UGT1A3, UGT1A8, UGT1A9, or UGT2B7. The effect of UGT induction (e.g., induction by rifampicin or any other UGT enzyme inducer) on empagliflozin exposure has not been evaluated. Empagliflozin is a substrate for P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP), but it does not inhibit these efflux transporters at therapeutic doses. Based on in vitro studies, empagliflozin is considered unlikely to cause interactions with drugs that are P-gp substrates. Empagliflozin is a substrate of the human uptake transporters OAT3, OATP1B1, and OATP1B3, but not OAT1 and OCT2. Empagliflozin does not inhibit any of these human uptake transporters at clinically relevant plasma concentrations and, therefore, no effect of empagliflozin is anticipated on concomitantly administered drugs that are substrates of these uptake transporters. In vivo Assessment of Drug Interactions Empagliflozin pharmacokinetics were similar with and without coadministration of metformin, glimepiride, pioglitazone, sitagliptin, linagliptin, warfarin, verapamil, ramipril, and simvastatin in healthy volunteers and with or without coadministration of hydrochlorothiazide and torsemide in patients with type 2 diabetes mellitus (see Figure 1 ). In subjects with normal renal function, coadministration of empagliflozin with probenecid resulted in a 30% decrease in the fraction of empagliflozin excreted in urine without any effect on 24-hour urinary glucose excretion. The relevance of this observation to patients with renal impairment is unknown. Figure 1 Effect of Various Medications on the Pharmacokinetics of Empagliflozin as Displayed as 90% Confidence Interval of Geometric Mean AUC and C max Ratios [reference lines indicate 100% (80% - 125%)] a empagliflozin, 50 mg, once daily; b empagliflozin, 25 mg, single dose; c empagliflozin, 25 mg, once daily; d empagliflozin, 10 mg, single dose Empagliflozin had no clinically relevant effect on the pharmacokinetics of metformin, glimepiride, pioglitazone, sitagliptin, linagliptin, warfarin, digoxin, ramipril, simvastatin, hydrochlorothiazide, torsemide, and oral contraceptives when coadministered in healthy volunteers (see Figure 2 ). Figure 2 Effect of Empagliflozin on the Pharmacokinetics of Various Medications as Displayed as 90% Confidence Interval of Geometric Mean AUC and C max Ratios [reference lines indicate 100% (80% - 125%)] a empagliflozin, 50 mg, once daily; b empagliflozin, 25 mg, once daily; c empagliflozin, 25 mg, single dose; d administered as simvastatin; e administered as warfarin racemic mixture; f administered as Microgynon ® ; g administered as ramipril Figure 1 Figure 2

12.1 Mechanism of Action Empagliflozin is an inhibitor of SGLT2, the predominant transporter responsible for reabsorption of glucose from the glomerular filtrate back into the circulation. By inhibiting SGLT2, empagliflozin reduces renal reabsorption of filtered glucose and lowers the renal threshold for glucose, and thereby increases urinary glucose excretion. Empagliflozin also reduces sodium reabsorption and increases the delivery of sodium to the distal tubule. This may influence several physiological functions including, but not restricted to, increasing tubuloglomerular feedback and reducing intraglomerular pressure, lowering both pre- and afterload of the heart and downregulating sympathetic activity.

12.2 Pharmacodynamics Urinary Glucose Excretion In patients with type 2 diabetes mellitus, urinary glucose excretion increased immediately following a dose of empagliflozin and was maintained at the end of a 4-week treatment period averaging at approximately 64 grams per day with 10 mg empagliflozin and 78 grams per day with 25 mg empagliflozin once daily [see Clinical Studies (14) ]. Data from single oral doses of empagliflozin in healthy subjects indicate that, on average, the elevation in urinary glucose excretion approaches baseline by about 3 days for the 10 mg and 25 mg doses. Urinary Volume In a 5-day study, mean 24-hour urine volume increase from baseline was 341 mL on Day 1 and 135 mL on Day 5 of empagliflozin 25 mg once daily treatment. Cardiac Electrophysiology In a randomized, placebo-controlled, active-comparator, crossover study, 30 healthy subjects were administered a single oral dose of empagliflozin 25 mg, empagliflozin 200 mg (8 times the maximum dose), moxifloxacin, and placebo. No increase in QTc was observed with either 25 mg or 200 mg empagliflozin.

12.3 Pharmacokinetics The pharmacokinetics of empagliflozin has been characterized in healthy volunteers and patients with type 2 diabetes mellitus and no clinically relevant differences were noted between the two populations. The steady-state mean plasma AUC and C max were 1,870 nmol∙h/L and 259 nmol/L, respectively, with 10 mg empagliflozin once daily treatment, and 4,740 nmol∙h/L and 687 nmol/L, respectively, with 25 mg empagliflozin once daily treatment. Systemic exposure of empagliflozin increased in a dose-proportional manner in the therapeutic dose range. Empagliflozin does not appear to have time-dependent pharmacokinetic characteristics. Following once-daily dosing, up to 22% accumulation, with respect to plasma AUC, was observed at steady-state. Absorption After oral administration, peak plasma concentrations of empagliflozin were reached at 1.5 hours post-dose. Administration of 25 mg empagliflozin after intake of a high-fat and high-calorie meal resulted in slightly lower exposure; AUC decreased by approximately 16% and C max decreased by approximately 37%, compared to fasted condition. The observed effect of food on empagliflozin pharmacokinetics was not considered clinically relevant and empagliflozin may be administered with or without food. Distribution The apparent steady-state volume of distribution was estimated to be 73.8 L based on a population pharmacokinetic analysis. Following administration of an oral [ 14 C]-empagliflozin solution to healthy subjects, the red blood cell partitioning was approximately 36.8% and plasma protein binding was 86.2%. Elimination The apparent terminal elimination half-life of empagliflozin was estimated to be 12.4 h and apparent oral clearance was 10.6 L/h based on the population pharmacokinetic analysis. Metabolism No major metabolites of empagliflozin were detected in human plasma and the most abundant metabolites were three glucuronide conjugates (2-O-, 3-O-, and 6-O-glucuronide). Systemic exposure of each metabolite was less than 10% of total drug-related material. In vitro studies suggested that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT2B7, UGT1A3, UGT1A8, and UGT1A9. Excretion Following administration of an oral [ 14 C]-empagliflozin solution to healthy subjects, approximately 95.6% of the drug-related radioactivity was eliminated in feces (41.2%) or urine (54.4%). The majority of drug-related radioactivity recovered in feces was unchanged parent drug and approximately half of drug-related radioactivity excreted in urine was unchanged parent drug. Specific Populations Pediatric Patients The pharmacokinetics and pharmacodynamics of empagliflozin were investigated in pediatric patients aged 10 to 17 years with type 2 diabetes mellitus. Oral administration of empagliflozin at 10 mg and 25 mg resulted in exposure within the range observed in adult patients. Effects of Age, Body Mass Index, Gender, and Race Age, body mass index (BMI), gender and race (Asians versus primarily Whites) do not have a clinically meaningful effect on pharmacokinetics of empagliflozin. Patients with Hepatic Impairment In adult patients with mild, moderate, and severe hepatic impairment according to the Child-Pugh classification, AUC of empagliflozin increased by approximately 23%, 47%, and 75%, and C max increased by approximately 4%, 23%, and 48%, respectively, compared to subjects with normal hepatic function.

h Hepatic Impairment In adult patients with mild, moderate, and severe hepatic impairment according to the Child-Pugh classification, AUC of empagliflozin increased by approximately 23%, 47%, and 75%, and C max increased by approximately 4%, 23%, and 48%, respectively, compared to subjects with normal hepatic function. Patients with Renal Impairment In adult patients with type 2 diabetes mellitus with mild (eGFR: 60 to less than 90 mL/min/1.73 m 2 ), moderate (eGFR: 30 to less than 60 mL/min/1.73 m 2 ), and severe (eGFR: less than 30 mL/min/1.73 m 2 ) renal impairment and patients on dialysis due to kidney failure, AUC of empagliflozin increased by approximately 18%, 20%, 66%, and 48%, respectively, compared to subjects with normal renal function. Peak plasma levels of empagliflozin were similar in patients with moderate renal impairment and patients on dialysis due to kidney failure compared to subjects with normal renal function. Peak plasma levels of empagliflozin were roughly 20% higher in patients with mild and severe renal impairment as compared to patients with normal renal function. Population pharmacokinetic analysis showed that the apparent oral clearance of empagliflozin decreased, with a decrease in eGFR leading to an increase in drug exposure. However, the fraction of empagliflozin that was excreted unchanged in urine, and urinary glucose excretion, declined with decrease in eGFR. Drug Interaction Studies In vitro Assessment of Drug Interactions Empagliflozin does not inhibit, inactivate, or induce CYP450 isoforms. In vitro data suggest that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT1A3, UGT1A8, UGT1A9, and UGT2B7. Empagliflozin does not inhibit UGT1A1, UGT1A3, UGT1A8, UGT1A9, or UGT2B7. Therefore, no effect of empagliflozin is anticipated on concomitantly administered drugs that are substrates of the major CYP450 isoforms or UGT1A1, UGT1A3, UGT1A8, UGT1A9, or UGT2B7. The effect of UGT induction (e.g., induction by rifampicin or any other UGT enzyme inducer) on empagliflozin exposure has not been evaluated. Empagliflozin is a substrate for P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP), but it does not inhibit these efflux transporters at therapeutic doses. Based on in vitro studies, empagliflozin is considered unlikely to cause interactions with drugs that are P-gp substrates. Empagliflozin is a substrate of the human uptake transporters OAT3, OATP1B1, and OATP1B3, but not OAT1 and OCT2. Empagliflozin does not inhibit any of these human uptake transporters at clinically relevant plasma concentrations and, therefore, no effect of empagliflozin is anticipated on concomitantly administered drugs that are substrates of these uptake transporters. In vivo Assessment of Drug Interactions Empagliflozin pharmacokinetics were similar with and without coadministration of metformin, glimepiride, pioglitazone, sitagliptin, linagliptin, warfarin, verapamil, ramipril, and simvastatin in healthy volunteers and with or without coadministration of hydrochlorothiazide and torsemide in patients with type 2 diabetes mellitus (see Figure 1 ). In subjects with normal renal function, coadministration of empagliflozin with probenecid resulted in a 30% decrease in the fraction of empagliflozin excreted in urine without any effect on 24-hour urinary glucose excretion. The relevance of this observation to patients with renal impairment is unknown.

see Figure 1 ). In subjects with normal renal function, coadministration of empagliflozin with probenecid resulted in a 30% decrease in the fraction of empagliflozin excreted in urine without any effect on 24-hour urinary glucose excretion. The relevance of this observation to patients with renal impairment is unknown. Figure 1 Effect of Various Medications on the Pharmacokinetics of Empagliflozin as Displayed as 90% Confidence Interval of Geometric Mean AUC and C max Ratios [reference lines indicate 100% (80% - 125%)] a empagliflozin, 50 mg, once daily; b empagliflozin, 25 mg, single dose; c empagliflozin, 25 mg, once daily; d empagliflozin, 10 mg, single dose Empagliflozin had no clinically relevant effect on the pharmacokinetics of metformin, glimepiride, pioglitazone, sitagliptin, linagliptin, warfarin, digoxin, ramipril, simvastatin, hydrochlorothiazide, torsemide, and oral contraceptives when coadministered in healthy volunteers (see Figure 2 ). Figure 2 Effect of Empagliflozin on the Pharmacokinetics of Various Medications as Displayed as 90% Confidence Interval of Geometric Mean AUC and C max Ratios [reference lines indicate 100% (80% - 125%)] a empagliflozin, 50 mg, once daily; b empagliflozin, 25 mg, once daily; c empagliflozin, 25 mg, single dose; d administered as simvastatin; e administered as warfarin racemic mixture; f administered as Microgynon ® ; g administered as ramipril Figure 1 Figure 2

<table ID="_Reffigure1" styleCode="Noautorules" width="75%"><caption>Figure 1 Effect of Various Medications on the Pharmacokinetics of Empagliflozin as Displayed as 90% Confidence Interval of Geometric Mean AUC and C_max Ratios [reference lines indicate 100% (80% - 125%)]</caption><col width="87%"/><tfoot><tr><td align="left" colspan="1" valign="top">^aempagliflozin, 50 mg, once daily; ^bempagliflozin, 25 mg, single dose; ^cempagliflozin, 25 mg, once daily; ^dempagliflozin, 10 mg, single dose</td></tr></tfoot><tbody><tr><td valign="top"><renderMultiMedia ID="id1739" referencedObject="MM2"/></td></tr></tbody></table> <table ID="_Reffigure2" styleCode="Noautorules" width="75%"><caption>Figure 2 Effect of Empagliflozin on the Pharmacokinetics of Various Medications as Displayed as 90% Confidence Interval of Geometric Mean AUC and C_max Ratios [reference lines indicate 100% (80% - 125%)]</caption><col width="87%"/><tfoot><tr><td align="left" colspan="1" valign="top">^aempagliflozin, 50 mg, once daily; ^bempagliflozin, 25 mg, once daily; ^cempagliflozin, 25 mg, single dose; ^dadministered as simvastatin; ^eadministered as warfarin racemic mixture; ^fadministered as Microgynon^&#xAE;; ^gadministered as ramipril</td></tr></tfoot><tbody><tr><td valign="top"><renderMultiMedia ID="id1760" referencedObject="MM3"/></td></tr></tbody></table>

13 NONCLINICAL TOXICOLOGY 13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility Carcinogenesis Carcinogenesis was evaluated in 2-year studies conducted in CD-1 mice and Wistar rats. Empagliflozin did not increase the incidence of tumors in female rats dosed at 100, 300, or 700 mg/kg/day (up to 72 times the exposure from the maximum clinical dose of 25 mg). In male rats, hemangiomas of the mesenteric lymph node were increased significantly at 700 mg/kg/day or approximately 42 times the exposure from a 25 mg clinical dose. Empagliflozin did not increase the incidence of tumors in female mice dosed at 100, 300, or 1,000 mg/kg/day (up to 62 times the exposure from a 25 mg clinical dose). Renal tubule adenomas and carcinomas were observed in male mice at 1,000 mg/kg/day, which is approximately 45 times the exposure of the maximum clinical dose of 25 mg. These tumors may be associated with a metabolic pathway predominantly present in the male mouse kidney. Mutagenesis Empagliflozin was not mutagenic or clastogenic with or without metabolic activation in the in vitro Ames bacterial mutagenicity assay, the in vitro L5178Y tk +/- mouse lymphoma cell assay, and an in vivo micronucleus assay in rats. Impairment of Fertility Empagliflozin had no effects on mating, fertility or early embryonic development in treated male or female rats up to the high dose of 700 mg/kg/day (approximately 155 times the 25 mg clinical dose in males and females, respectively).

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility Carcinogenesis Carcinogenesis was evaluated in 2-year studies conducted in CD-1 mice and Wistar rats. Empagliflozin did not increase the incidence of tumors in female rats dosed at 100, 300, or 700 mg/kg/day (up to 72 times the exposure from the maximum clinical dose of 25 mg). In male rats, hemangiomas of the mesenteric lymph node were increased significantly at 700 mg/kg/day or approximately 42 times the exposure from a 25 mg clinical dose. Empagliflozin did not increase the incidence of tumors in female mice dosed at 100, 300, or 1,000 mg/kg/day (up to 62 times the exposure from a 25 mg clinical dose). Renal tubule adenomas and carcinomas were observed in male mice at 1,000 mg/kg/day, which is approximately 45 times the exposure of the maximum clinical dose of 25 mg. These tumors may be associated with a metabolic pathway predominantly present in the male mouse kidney. Mutagenesis Empagliflozin was not mutagenic or clastogenic with or without metabolic activation in the in vitro Ames bacterial mutagenicity assay, the in vitro L5178Y tk +/- mouse lymphoma cell assay, and an in vivo micronucleus assay in rats. Impairment of Fertility Empagliflozin had no effects on mating, fertility or early embryonic development in treated male or female rats up to the high dose of 700 mg/kg/day (approximately 155 times the 25 mg clinical dose in males and females, respectively).

14 CLINICAL STUDIES 14.1 Glycemic Control Trials in Adults with Type 2 Diabetes Mellitus JARDIANCE has been studied as monotherapy and in combination with metformin, sulfonylurea, pioglitazone, linagliptin, and insulin. JARDIANCE has also been studied in patients with type 2 diabetes mellitus with mild or moderate renal impairment. In adult patients with type 2 diabetes mellitus, treatment with JARDIANCE reduced hemoglobin A1c (HbA1c), compared to placebo. The reduction in HbA1c for JARDIANCE compared with placebo was observed across subgroups including sex, race, geographic region, baseline BMI and duration of disease. Monotherapy A total of 986 patients with type 2 diabetes mellitus participated in a double-blind, placebo-controlled trial to evaluate the efficacy of JARDIANCE monotherapy. Treatment-naïve patients with inadequately controlled type 2 diabetes mellitus entered an open-label placebo run-in for 2 weeks. At the end of the run-in period, patients who remained inadequately controlled and had an HbA1c between 7% and 10% were randomized to placebo, JARDIANCE 10 mg, JARDIANCE 25 mg, or a reference comparator. At Week 24, treatment with JARDIANCE 10 mg or 25 mg daily provided statistically significant reductions in HbA1c (p-value <0.0001), fasting plasma glucose (FPG), and body weight compared with placebo (see Table 5 and Figure 3 ). Table 5Results at Week 24 From a Placebo-Controlled Monotherapy Trial of JARDIANCE JARDIANCE 10 mg N=224 JARDIANCE 25 mg N=224 Placebo N=228 a Modified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 9.4%, 9.4%, and 30.7% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA derived p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) c FPG (mg/dL); for JARDIANCE 10 mg, n=223, for JARDIANCE 25 mg, n=223, and for placebo, n=226 HbA1c (%) a Baseline (mean) 7.9 7.9 7.9 Change from baseline (adjusted mean) -0.7 -0.8 0.1 Difference from placebo (adjusted mean) (97.5% CI) -0.7 b (-0.9, -0.6) -0.9 b (-1.0, -0.7) -- Patients [n (%)] achieving HbA1c <7% 72 (35%) 88 (44%) 25 (12%) FPG (mg/dL) c Baseline (mean) 153 153 155 Change from baseline (adjusted mean) -19 -25 12 Difference from placebo (adjusted mean) (95% CI) -31 (-37, -26) -36 (-42, -31) -- Body Weight Baseline (mean) in kg 78 78 78 % change from baseline (adjusted mean) -2.8 -3.2 -0.4 Difference from placebo (adjusted mean) (95% CI) -2.5 b (-3.1, -1.9) -2.8 b (-3.4, -2.2) -- Figure 3 Adjusted Mean HbA1c Change at Each Time Point (Completers) and at Week 24 (mITT Population) - LOCF At Week 24, the systolic blood pressure was statistically significantly reduced compared to placebo by -2.6 mmHg (placebo-adjusted, p-value=0.0231) in patients randomized to 10 mg of JARDIANCE and by -3.4 mmHg (placebo-corrected, p-value=0.0028) in patients randomized to 25 mg of JARDIANCE. Figure 3 Add-On Combination Therapy with Metformin A total of 637 patients with type 2 diabetes mellitus participated in a double-blind, placebo-controlled trial to evaluate the efficacy of JARDIANCE in combination with metformin. Patients with type 2 diabetes mellitus inadequately controlled on at least 1,500 mg of metformin per day entered an open-label 2-week placebo run-in.

f 637 patients with type 2 diabetes mellitus participated in a double-blind, placebo-controlled trial to evaluate the efficacy of JARDIANCE in combination with metformin. Patients with type 2 diabetes mellitus inadequately controlled on at least 1,500 mg of metformin per day entered an open-label 2-week placebo run-in. At the end of the run-in period, patients who remained inadequately controlled and had an HbA1c between 7% and 10% were randomized to placebo, JARDIANCE 10 mg, or JARDIANCE 25 mg. At Week 24, treatment with JARDIANCE 10 mg or 25 mg daily provided statistically significant reductions in HbA1c (p-value <0.0001), FPG, and body weight compared with placebo (see Table 6 ). Table 6Results at Week 24 From a Placebo-Controlled Trial for JARDIANCE used in Combination with Metformin JARDIANCE 10 mg N=217 JARDIANCE 25 mg N=213 Placebo N=207 a Modified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 9.7%, 14.1%, and 24.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) c FPG (mg/dL); for JARDIANCE 10 mg, n=216, for JARDIANCE 25 mg, n=213, and for placebo, n=207 HbA1c (%) a Baseline (mean) 7.9 7.9 7.9 Change from baseline (adjusted mean) -0.7 -0.8 -0.1 Difference from placebo + metformin (adjusted mean) (95% CI) -0.6 b (-0.7, -0.4) -0.6 b (-0.8, -0.5) -- Patients [n (%)] achieving HbA1c <7% 75 (38%) 74 (39%) 23 (13%) FPG (mg/dL) c Baseline (mean) 155 149 156 Change from baseline (adjusted mean) -20 -22 6 Difference from placebo + metformin (adjusted mean) -26 -29 -- Body Weight Baseline mean in kg 82 82 80 % change from baseline (adjusted mean) -2.5 -2.9 -0.5 Difference from placebo (adjusted mean) (95% CI) -2.0 b (-2.6, -1.4) -2.5 b (-3.1, -1.9) -- At Week 24, the systolic blood pressure was statistically significantly reduced compared to placebo by -4.1 mmHg (placebo-corrected, p-value <0.0001) for JARDIANCE 10 mg and -4.8 mmHg (placebo-corrected, p-value <0.0001) for JARDIANCE 25 mg. Initial Combination Therapy with Metformin A total of 1,364 patients with type 2 diabetes mellitus participated in a double-blind, randomized, active-controlled trial to evaluate the efficacy of JARDIANCE in combination with metformin as initial therapy compared to the corresponding individual components. Treatment-naïve patients with inadequately controlled type 2 diabetes mellitus entered an open-label placebo run-in for 2 weeks. At the end of the run-in period, patients who remained inadequately controlled and had an HbA1c between 7% and 10.5% were randomized to one of 8 active-treatment arms: JARDIANCE 10 mg or 25 mg; metformin 1,000 mg, or 2,000 mg; JARDIANCE 10 mg in combination with 1,000 mg or 2,000 mg metformin; or JARDIANCE 25 mg in combination with 1,000 mg or 2,000 mg metformin. At Week 24, initial therapy of JARDIANCE in combination with metformin provided statistically significant reductions in HbA1c (p-value <0.01) compared to the individual components (see Table 7 ). Table 7Glycemic Parameters at 24 Weeks in a Trial Comparing JARDIANCE and Metformin to the Individual Components as Initial Therapy JARDIANCE 10 mg + Metformin 1,000 mg a N=161 JARDIANCE 10 mg + Metformin 2,000 mg a N=167 JARDIANCE 25 mg + Metformin 1,000 mg a N=165 JARDIANCE 25 mg + Metformin 2,000 mg a N=169 JARDIANCE 10 mg N=169 JARDIANCE 25 mg N=163 Metformin 1,000 mg a N=167 Metformin 2,000 mg a N=162 a Metformin total daily dose, administered in two equally divided doses per day.

N=161 JARDIANCE 10 mg + Metformin 2,000 mg a N=167 JARDIANCE 25 mg + Metformin 1,000 mg a N=165 JARDIANCE 25 mg + Metformin 2,000 mg a N=169 JARDIANCE 10 mg N=169 JARDIANCE 25 mg N=163 Metformin 1,000 mg a N=167 Metformin 2,000 mg a N=162 a Metformin total daily dose, administered in two equally divided doses per day. b p-value ≤0.0062 (modified intent-to-treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c). c p-value ≤0.0056 (modified intent-to-treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c). HbA1c (%) Baseline (mean) 8.7 8.7 8.8 8.7 8.6 8.9 8.7 8.6 Change from baseline (adjusted mean) -2.0 -2.1 -1.9 -2.1 -1.4 -1.4 -1.2 -1.8 Comparison vs JARDIANCE (adjusted mean) (95% CI) -0.6 b (-0.9, -0.4) -0.7 b (-1.0, -0.5) -0.6 c (-0.8, -0.3) -0.7 c (-1.0, -0.5) -- -- -- -- Comparison vs metformin (adjusted mean) (95% CI) -0.8 b (-1.0, -0.6) -0.3 b (-0.6, -0.1) -0.8 c (-1.0, -0.5) -0.3 c (-0.6, -0.1) -- -- -- -- Add-On Combination Therapy with Metformin and Sulfonylurea A total of 666 patients with type 2 diabetes mellitus participated in a double-blind, placebo-controlled trial to evaluate the efficacy of JARDIANCE in combination with metformin plus a sulfonylurea. Patients with inadequately controlled type 2 diabetes mellitus on at least 1,500 mg per day of metformin and on a sulfonylurea, entered a 2-week open-label placebo run-in. At the end of the run-in, patients who remained inadequately controlled and had an HbA1c between 7% and 10% were randomized to placebo, JARDIANCE 10 mg, or JARDIANCE 25 mg. Treatment with JARDIANCE 10 mg or 25 mg daily provided statistically significant reductions in HbA1c (p-value <0.0001), FPG, and body weight compared with placebo (see Table 8 ). Table 8Results at Week 24 from a Placebo-Controlled Trial for JARDIANCE in Combination with Metformin and Sulfonylurea JARDIANCE 10 mg N=225 JARDIANCE 25 mg N=216 Placebo N=225 a Modified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 17.8%, 16.7%, and 25.3% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) c FPG (mg/dL); for JARDIANCE 10 mg, n=225, for JARDIANCE 25 mg, n=215, for placebo, n=224 HbA1c (%) a Baseline (mean) 8.1 8.1 8.2 Change from baseline (adjusted mean) -0.8 -0.8 -0.2 Difference from placebo (adjusted mean) (95% CI) -0.6 b (-0.8, -0.5) -0.6 b (-0.7, -0.4) -- Patients [n (%)] achieving HbA1c <7% 55 (26%) 65 (32%) 20 (9%) FPG (mg/dL) c Baseline (mean) 151 156 152 Change from baseline (adjusted mean) -23 -23 6 Difference from placebo (adjusted mean) -29 -29 -- Body Weight Baseline mean in kg 77 78 76 % change from baseline (adjusted mean) -2.9 -3.2 -0.5 Difference from placebo (adjusted mean) (95% CI) -2.4 b (-3.0, -1.8) -2.7 b (-3.3, -2.1) -- In Combination with Linagliptin as Add-On to Metformin Therapy A total of 686 patients with type 2 diabetes mellitus participated in a double-blind, active-controlled trial to evaluate the efficacy of JARDIANCE 10 mg or 25 mg in combination with linagliptin 5 mg compared to the individual components. Patients with type 2 diabetes mellitus inadequately controlled on at least 1,500 mg of metformin per day entered a single-blind placebo run-in period for 2 weeks.

ind, active-controlled trial to evaluate the efficacy of JARDIANCE 10 mg or 25 mg in combination with linagliptin 5 mg compared to the individual components. Patients with type 2 diabetes mellitus inadequately controlled on at least 1,500 mg of metformin per day entered a single-blind placebo run-in period for 2 weeks. At the end of the run-in period, patients who remained inadequately controlled and had an HbA1c between 7% and 10.5% were randomized 1:1:1:1:1 to one of 5 active-treatment arms of JARDIANCE 10 mg or 25 mg, linagliptin 5 mg, or linagliptin 5 mg in combination with 10 mg or 25 mg JARDIANCE as a fixed-dose combination tablet. At Week 24, JARDIANCE 10 mg or 25 mg used in combination with linagliptin 5 mg provided statistically significant improvement in HbA1c (p-value <0.0001) and FPG (p-value <0.001) compared to the individual components in patients who had been inadequately controlled on metformin. Treatment with JARDIANCE/linagliptin 25 mg/5 mg or JARDIANCE/linagliptin 10 mg/5 mg daily also resulted in a statistically significant reduction in body weight compared to linagliptin 5 mg (p-value <0.0001). There was no statistically significant difference in body weight compared to JARDIANCE alone. Active-Controlled Trial versus Glimepiride in Combination with Metformin The efficacy of JARDIANCE was evaluated in a double-blind, glimepiride-controlled, trial in 1,545 patients with type 2 diabetes mellitus with insufficient glycemic control despite metformin therapy. Patients with inadequate glycemic control and an HbA1c between 7% and 10% after a 2-week run-in period were randomized to glimepiride or JARDIANCE 25 mg. At Week 52, JARDIANCE 25 mg and glimepiride lowered HbA1c and FPG (see Table 9 , Figure 4 ). The difference in observed effect size between JARDIANCE 25 mg and glimepiride excluded the pre-specified non-inferiority margin of 0.3%. The mean daily dosage of glimepiride was 2.7 mg and the maximal approved dosage in the United States is 8 mg per day. Table 9Results at Week 52 from an Active-Controlled Trial Comparing JARDIANCE to Glimepiride as Add-On Therapy in Patients Inadequately Controlled on Metformin JARDIANCE 25 mg N=765 Glimepiride N=780 a Modified intent-to-treat population. Last observation on trial (LOCF) was used to impute data missing at Week 52. At Week 52, data was imputed for 15.3% and 21.9% of patients randomized to JARDIANCE 25 mg and glimepiride, respectively. b Non-inferior, ANCOVA model p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region) c ANCOVA p-value <0.0001 (Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) d FPG (mg/dL); for JARDIANCE 25 mg, n=764, for glimepiride, n=779 HbA1c (%) a Baseline (mean) 7.9 7.9 Change from baseline (adjusted mean) -0.7 -0.7 Difference from glimepiride (adjusted mean) (97.5% CI) -0.07 b (-0.15, 0.01) -- FPG (mg/dL) d Baseline (mean) 150 150 Change from baseline (adjusted mean) -19 -9 Difference from glimepiride (adjusted mean) -11 -- Body Weight Baseline mean in kg 82.5 83 % change from baseline (adjusted mean) -3.9 2.0 Difference from glimepiride (adjusted mean) (95% CI) -5.9 c (-6.3, -5.5) -- Figure 4 Adjusted mean HbA1c Change at Each Time Point (Completers) and at Week 52 (mITT Population) - LOCF At Week 52, the adjusted mean change from baseline in systolic blood pressure was -3.6 mmHg, compared to 2.2 mmHg for glimepiride. The differences between treatment groups for systolic blood pressure was statistically significant (p-value <0.0001). At Week 104, the adjusted mean change from baseline in HbA1c was -0.75% for JARDIANCE 25 mg and -0.66% for glimepiride.

ne in systolic blood pressure was -3.6 mmHg, compared to 2.2 mmHg for glimepiride. The differences between treatment groups for systolic blood pressure was statistically significant (p-value <0.0001). At Week 104, the adjusted mean change from baseline in HbA1c was -0.75% for JARDIANCE 25 mg and -0.66% for glimepiride. The adjusted mean treatment difference was -0.09% with a 97.5% confidence interval of (-0.32%, 0.15%), excluding the pre-specified non-inferiority margin of 0.3%. The mean daily dosage of glimepiride was 2.7 mg and the maximal approved dosage in the United States is 8 mg per day. The Week 104 analysis included data with and without concomitant glycemic rescue medication, as well as off-treatment data. Missing data for patients not providing any information at the visit were imputed based on the observed off-treatment data. In this multiple imputation analysis, 13.9% of the data were imputed for JARDIANCE 25 mg and 12.9% for glimepiride. At Week 104, JARDIANCE 25 mg daily resulted in a statistically significant difference in change from baseline for body weight compared to glimepiride (-3.1 kg for JARDIANCE 25 mg vs. +1.3 kg for glimepiride; ANCOVA-LOCF, p-value <0.0001). Figure 4 Add-On Combination Therapy with Pioglitazone with or without Metformin A total of 498 patients with type 2 diabetes mellitus participated in a double-blind, placebo-controlled trial to evaluate the efficacy of JARDIANCE in combination with pioglitazone, with or without metformin. Patients with inadequately controlled type 2 diabetes mellitus on metformin at a dose of at least 1,500 mg per day and pioglitazone at a dose of at least 30 mg per day were placed into an open-label placebo run-in for 2 weeks. Patients with inadequate glycemic control and an HbA1c between 7% and 10% after the run-in period were randomized to placebo, JARDIANCE 10 mg, or JARDIANCE 25 mg. Treatment with JARDIANCE 10 mg or 25 mg daily resulted in statistically significant reductions in HbA1c (p-value <0.0001), FPG, and body weight compared with placebo (see Table 10 ). Table 10Results of Placebo-Controlled Trial for JARDIANCE in Combination Therapy with Pioglitazone JARDIANCE 10 mg N=165 JARDIANCE 25 mg N=168 Placebo N=165 a Modified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 10.9%, 8.3%, and 20.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and background medication. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) c FPG (mg/dL); for JARDIANCE 10 mg, n=163 HbA1c (%) a Baseline (mean) 8.1 8.1 8.2 Change from baseline (adjusted mean) -0.6 -0.7 -0.1 Difference from placebo + pioglitazone (adjusted mean) (95% CI) -0.5 b (-0.7, -0.3) -0.6 b (-0.8, -0.4) -- Patients [n (%)] achieving HbA1c <7% 36 (24%) 48 (30%) 12 (8%) FPG (mg/dL) c Baseline (mean) 152 152 152 Change from baseline (adjusted mean) -17 -22 7 Difference from placebo + pioglitazone (adjusted mean) (97.5% CI) -23 b (-31.8, -15.2) -28 b (-36.7, -20.2) -- Body Weight Baseline mean in kg 78 79 78 % change from baseline (adjusted mean) -2.0 -1.8 0.6 Difference from placebo (adjusted mean) (95% CI) -2.6 b (-3.4, -1.8) -2.4 b (-3.2, -1.6) -- Add-On Combination with Insulin with or without Metformin and/or Sulfonylureas A total of 494 patients with type 2 diabetes mellitus inadequately controlled on insulin, or insulin in combination with oral drugs participated in a double-blind, placebo-controlled trial to evaluate the efficacy of JARDIANCE as add-on therapy to insulin over 78 weeks.

in with or without Metformin and/or Sulfonylureas A total of 494 patients with type 2 diabetes mellitus inadequately controlled on insulin, or insulin in combination with oral drugs participated in a double-blind, placebo-controlled trial to evaluate the efficacy of JARDIANCE as add-on therapy to insulin over 78 weeks. Patients entered a 2-week placebo run-in period on basal insulin (e.g., insulin glargine, insulin detemir, or NPH insulin) with or without metformin and/or sulfonylurea background therapy. Following the run-in period, patients with inadequate glycemic control were randomized to the addition of JARDIANCE 10 mg, JARDIANCE 25 mg, or placebo. Patients were maintained on a stable dose of insulin prior to enrollment, during the run-in period, and during the first 18 weeks of treatment. For the remaining 60 weeks, insulin could be adjusted. The mean total daily insulin dose at baseline for JARDIANCE 10 mg, 25 mg, and placebo was 45 IU, 48 IU, and 48 IU, respectively. JARDIANCE used in combination with insulin (with or without metformin and/or sulfonylurea) provided statistically significant reductions in HbA1c and FPG compared to placebo after both 18 and 78 weeks of treatment (see Table 11 ). JARDIANCE 10 mg or 25 mg daily also resulted in statistically significantly greater percent body weight reduction compared to placebo. Table 11Results at Week 18 and 78 for a Placebo-Controlled Trial for JARDIANCE in Combination with Insulin 18 weeks (no insulin adjustment) 78 weeks (adjustable insulin dose after 18 weeks) JARDIANCE 10 mg N=169 JARDIANCE 25 mg N=155 Placebo N=170 JARDIANCE 10 mg N=169 JARDIANCE 25 mg N=155 Placebo N=170 a Modified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 18 and 78. At Week 18, 21.3%, 30.3%, and 21.8% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. At Week 78, 32.5%, 38.1% and 42.4% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, and region; FPG: MMRM model includes baseline FPG, baseline HbA1c, treatment, region, visit and visit by treatment interaction. Body weight: MMRM model includes baseline body weight, baseline HbA1c, treatment, region, visit and visit by treatment interaction. c p-value=0.0049 d p-value=0.0052 e p-value=0.0463 HbA1c (%) a Baseline (mean) 8.3 8.3 8.2 8.3 8.3 8.2 Change from baseline (adjusted mean) -0.6 -0.7 0 -0.4 -0.6 0.1 Difference from placebo (adjusted mean) (97.5% CI) -0.6 b (-0.8, -0.4) -0.7 b (-0.9, -0.5) -- -0.5 b (-0.7, -0.3) -0.7 b (-0.9, -0.5) -- Patients (%) achieving HbA1c <7% 18.0 19.5 5.5 12.0 17.5 6.7 FPG (mg/dL) Baseline (mean) 138 146 142 138 146 142 Change from baseline (adjusted mean, SE) -17.9 (3.2) -19.1 (3.3) 10.4 (3.1) -10.1 (3.2) -15.2 (3.4) 2.8 (3.2) Difference from placebo (adjusted mean) (95% CI) -28.2 b (-37.0, -19.5) -29.5 b (-38.4, -20.6) -- -12.9 c (-21.9, 3.9) -17.9 b (-27.0, -8.8) -- Body Weight Baseline mean in kg 92 95 90 92 95 90 % change from baseline (adjusted mean) -1.8 -1.4 -0.1 -2.4 -2.4 0.7 Difference from placebo (adjusted mean) (95% CI) -1.7 d (-3.0, -0.5) -1.3 e (-2.5, -0.0) -- -3.0 b (-4.4, -1.7) -3.0 b (-4.4, -1.6) -- Add-on Combination with MDI Insulin with or without Metformin A total of 563 patients with type 2 diabetes mellitus inadequately controlled on multiple daily injections (MDI) of insulin (total daily dose >60 IU), alone or in combination with metformin, participated in a double-blind, placebo-controlled trial to evaluate the efficacy of JARDIANCE as add-on therapy to MDI insulin over 18 weeks.

3 patients with type 2 diabetes mellitus inadequately controlled on multiple daily injections (MDI) of insulin (total daily dose >60 IU), alone or in combination with metformin, participated in a double-blind, placebo-controlled trial to evaluate the efficacy of JARDIANCE as add-on therapy to MDI insulin over 18 weeks. Patients entered a 2-week placebo run-in period on MDI insulin with or without metformin background therapy. Following the run-in period, patients with inadequate glycemic control were randomized to the addition of JARDIANCE 10 mg, JARDIANCE 25 mg, or placebo. Patients were maintained on a stable dose of insulin prior to enrollment, during the run-in period, and during the first 18 weeks of treatment. The mean total daily insulin dose at baseline for JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo was 88.6 IU, 90.4 IU, and 89.9 IU, respectively. JARDIANCE 10 mg or 25 mg daily used in combination with MDI insulin (with or without metformin) provided statistically significant reductions in HbA1c compared to placebo after 18 weeks of treatment (see Table 12 ). Table 12Results at Week 18 for a Placebo-Controlled Trial for JARDIANCE in Combination with Insulin and with or without Metformin JARDIANCE 10 mg N=186 JARDIANCE 25 mg N=189 Placebo N=188 a Modified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 18. At Week 18, 23.7%, 22.8% and 23.4% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, geographical region, and background medication). HbA1c (%) a Baseline (mean) 8.4 8.3 8.3 Change from baseline (adjusted mean) -0.9 -1.0 -0.5 Difference from placebo (adjusted mean) (95% CI) -0.4 b (-0.6, -0.3) -0.5 b (-0.7, -0.4) -- During an extension period with treatment for up to 52 weeks, insulin could be adjusted to achieve defined glucose target levels. The change from baseline in HbA1c was maintained from 18 to 52 weeks with both JARDIANCE 10 mg and 25 mg. After 52 weeks, JARDIANCE 10 mg or 25 mg daily resulted in statistically greater percent body weight reduction compared to placebo (p-value <0.0001). The mean change in body weight from baseline was -1.95 kg for JARDIANCE 10 mg, and -2.04 kg for JARDIANCE 25 mg. Renal Impairment A total of 738 patients with type 2 diabetes mellitus and a baseline eGFR less than 90 mL/min/1.73 m 2 participated in a randomized, double-blind, placebo-controlled, parallel-group trial to evaluate the efficacy of JARDIANCE in patients with type 2 diabetes mellitus and renal impairment. The trial population comprised of 290 patients with mild renal impairment (eGFR 60 to less than 90 mL/min/1.73 m 2 ), 374 patients with moderate renal impairment (eGFR 30 to less than 60 mL/min/1.73 m 2 ), and 74 with severe renal impairment (eGFR less than 30 mL/min/1.73 m 2 ). A total of 194 patients with moderate renal impairment had a baseline eGFR of 30 to less than 45 mL/min/1.73 m 2 and 180 patients had a baseline eGFR of 45 to less than 60 mL/min/1.73 m 2 . At Week 24, JARDIANCE 25 mg provided statistically significant reduction in HbA1c relative to placebo in patients with mild to moderate renal impairment (see Table 13 ). A statistically significant reduction relative to placebo was also observed with JARDIANCE 25 mg in patients with either mild [-0.7 (95% CI: -0.9, -0.5)] or moderate [-0.4 (95% CI: -0.6, -0.3)] renal impairment and with JARDIANCE 10 mg in patients with mild [-0.5 (95% CI: -0.7, -0.3)] renal impairment. The glucose lowering efficacy of JARDIANCE 25 mg decreased with decreasing level of renal function in the mild to moderate range.

either mild [-0.7 (95% CI: -0.9, -0.5)] or moderate [-0.4 (95% CI: -0.6, -0.3)] renal impairment and with JARDIANCE 10 mg in patients with mild [-0.5 (95% CI: -0.7, -0.3)] renal impairment. The glucose lowering efficacy of JARDIANCE 25 mg decreased with decreasing level of renal function in the mild to moderate range. Least square mean HbA1c changes at 24 weeks were -0.6%, -0.5%, and -0.2% for those with a baseline eGFR of 60 to less than 90 mL/min/1.73 m 2 , 45 to less than 60 mL/min/1.73 m 2 , and 30 to less than 45 mL/min/1.73 m 2 , respectively [see Dosage and Administration (2) and Use in Specific Populations (8.6) ] . For placebo, least square mean HbA1c changes at 24 weeks were 0.1%, -0.1%, and 0.2% for patients with a baseline eGFR of 60 to less than 90 mL/min/1.73 m 2 , 45 to less than 60 mL/min/1.73 m 2 , and 30 to less than 45 mL/min/1.73 m 2 , respectively. Table 13Results at Week 24 (LOCF) of Placebo-Controlled Trial for JARDIANCE in Adults with Type 2 Diabetes Mellitus and Renal Impairment Mild and Moderate Impairment b JARDIANCE 25 mg a p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and background medication) b eGFR 30 to less than 90 mL/min/1.73 m 2 - Modified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 24.6% and 26.2% was imputed for patients randomized to JARDIANCE 25 mg and placebo, respectively. HbA1c Number of patients n=284 Comparison vs placebo (adjusted mean) (95% CI) -0.5 a (-0.6, -0.4) For patients with severe renal impairment, the analyses of changes in HbA1c and FPG showed no discernible treatment effect of JARDIANCE 25 mg compared to placebo [see Indications and Usage (1) , Dosage and Administration (2.1 , 2.2) and Use in Specific Populations (8.6) ] . 14.2 Glycemic Control Trial in Pediatric Patients Aged 10 to 17 Years with Type 2 Diabetes Mellitus DINAMO (NCT03429543) was a 26-week, double-blind, randomized, placebo-controlled, parallel group trial, with a double-blind active treatment safety extension period up to 52 weeks to assess the efficacy of JARDIANCE. The trial enrolled pediatric patients aged 10 to 17 years with inadequately controlled type 2 diabetes mellitus (HbA1c 6.5 to 10.5%). Patients treated with metformin (at least 1,000 mg daily or maximally tolerated dose), with or without insulin therapy, and those with a history of intolerance to metformin therapy were enrolled. Patients were randomized to 3 treatment arms (JARDIANCE 10 mg, a dipeptidyl peptidase-4 (DPP-4) inhibitor or placebo), over 26 weeks. Patients in the JARDIANCE 10 mg group who failed to achieve HbA1c <7.0% at Week 12 underwent a second randomization at Week 14 to remain on the 10 mg dose or increase to 25 mg. Patients on placebo were re-randomized at Week 26 to one of the JARDIANCE doses (10 mg or 25 mg) or a DPP-4 inhibitor. A total of 157 patients were treated with either JARDIANCE (10 mg or 25 mg; N=52), a DPP-4 inhibitor (N=52), or placebo (N=53). Background therapies as adjunct to diet and exercise included metformin (51%), a combination of metformin and insulin (40.1%), insulin (3.2%), or none (5.7%). The mean HbA1c at baseline was 8.0% and the mean duration of type 2 diabetes mellitus was 2.1 years. The mean age was 14.5 years (range: 10-17 years) and 51.6% were aged 15 years and older. Approximately, 50% were White, 6% were Asian, 31% were Black or African American, and 38% were of Hispanic or Latino ethnicity. The mean BMI was 36.0 kg/m 2 and mean BMI Z-score was 3.0. Patients with an eGFR less than 60 mL/min/1.73 m 2 were not enrolled in the trial. Approximately 25% of the study population had microalbuminuria or macroalbuminuria.

were Asian, 31% were Black or African American, and 38% were of Hispanic or Latino ethnicity. The mean BMI was 36.0 kg/m 2 and mean BMI Z-score was 3.0. Patients with an eGFR less than 60 mL/min/1.73 m 2 were not enrolled in the trial. Approximately 25% of the study population had microalbuminuria or macroalbuminuria. At Week 26, treatment with JARDIANCE was superior in reducing HbA1c from baseline versus placebo (see Table 14 ). Table 14Results at Week 26 for a Placebo-Controlled Trial for JARDIANCE in Combination with Metformin and/or Insulin or as Monotherapy in Pediatric Patients Aged 10 to 17 Years with Type 2 Diabetes Mellitus a JARDIANCE 10 mg and 25 mg Placebo a Modified intent-to-treat set (All randomized and treated patients with baseline measurement). b Multiple imputations using placebo wash-out approach with 500 iterations for missing data. Imputed for HbA1c (Jardiance N=5 (9.6 %), Placebo N=3 (5.7%)), for FPG (Jardiance N=4 (8.3%), Placebo N=2 (3.8%)). c Least-Square Mean from Analysis of Covariance (ANCOVA) adjusted for baseline value and baseline age stratum (< 15 years vs 15 to < 18 years). d Not evaluated for statistical significance, not part of sequential testing procedure. e p-value=0.0116 (two-sided) HbA1c (%) b Number of patients n=52 n=53 Baseline (mean) 8.0 8.1 Change from baseline c -0.2 0.7 Difference from placebo c (95% CI) -0.8 e (-1.5, -0.2) -- FPG (mg/dL) b,d Number of patients n=48 n=52 Baseline (mean) 154 159 Change from baseline c -19 17 Difference from placebo c (95% CI) -36 (-60.7, -10.7) -- 14.3 Cardiovascular Outcomes in Adults with Type 2 Diabetes Mellitus and Atherosclerotic Cardiovascular Disease The effect of JARDIANCE on cardiovascular (CV) risk in adult patients with type 2 diabetes mellitus and established, stable, atherosclerotic CV disease was evaluated in the EMPA-REG OUTCOME trial, a multicenter, multinational, randomized, double-blind parallel group trial. The trial compared the risk of experiencing a major adverse cardiovascular event (MACE) between JARDIANCE and placebo when these were added to and used concomitantly with standard of care treatments for diabetes mellitus and atherosclerotic CV disease. Concomitant antidiabetic medications were to be kept stable for the first 12 weeks of the trial. Thereafter, antidiabetic and atherosclerotic therapies could be adjusted, at the discretion of investigators, to ensure participants were treated according to the standard care for these diseases. A total of 7,020 patients were treated (JARDIANCE 10 mg = 2,345; JARDIANCE 25 mg = 2,342; placebo = 2,333) and followed for a median of 3.1 years. Approximately 72% of the trial population was White, 22% was Asian, and 5% was Black. The mean age was 63 years and approximately 72% were male. All patients in the trial had inadequately controlled type 2 diabetes mellitus at baseline (HbA1c greater than or equal to 7%). The mean HbA1c at baseline was 8.1% and 57% of participants had diabetes mellitus for more than 10 years. Approximately 31%, 22% and 20% reported a past history of neuropathy, retinopathy and nephropathy to investigators, respectively and the mean eGFR was 74 mL/min/1.73 m 2 . At baseline, patients were treated with one (~30%) or more (~70%) antidiabetic medications including metformin (74%), insulin (48%), and sulfonylurea (43%). All patients had established atherosclerotic CV disease at baseline including one (82%) or more (18%) of the following: a documented history of coronary artery disease (76%), stroke (23%) or peripheral artery disease (21%). At baseline, the mean systolic blood pressure was 136 mmHg, the mean diastolic blood pressure was 76 mmHg, the mean LDL was 86 mg/dL, the mean HDL was 44 mg/dL, and the mean urinary albumin to creatinine ratio (UACR) was 175 mg/g.

istory of coronary artery disease (76%), stroke (23%) or peripheral artery disease (21%). At baseline, the mean systolic blood pressure was 136 mmHg, the mean diastolic blood pressure was 76 mmHg, the mean LDL was 86 mg/dL, the mean HDL was 44 mg/dL, and the mean urinary albumin to creatinine ratio (UACR) was 175 mg/g. At baseline, approximately 81% of patients were treated with renin angiotensin system inhibitors, 65% with beta-blockers, 43% with diuretics, 77% with statins, and 86% with antiplatelet agents (mostly aspirin). The primary endpoint in EMPA-REG OUTCOME was the time to first occurrence of a Major Adverse Cardiac Event (MACE). A major adverse cardiac event was defined as occurrence of either a CV death or a non-fatal myocardial infarction (MI) or a non-fatal stroke. The statistical analysis plan had pre-specified that the 10 and 25 mg doses would be combined. A Cox proportional hazards model was used to test for non-inferiority against the pre-specified risk margin of 1.3 for the hazard ratio of MACE and superiority on MACE if non-inferiority was demonstrated. Type-1 error was controlled across multiples tests using a hierarchical testing strategy. JARDIANCE significantly reduced the risk of first occurrence of primary composite endpoint of CV death, non-fatal myocardial infarction, or non-fatal stroke (HR: 0.86; 95% CI: 0.74, 0.99). The treatment effect was due to a significant reduction in the risk of CV death in subjects randomized to empagliflozin (HR: 0.62; 95% CI: 0.49, 0.77), with no change in the risk of non-fatal myocardial infarction or non-fatal stroke (see Table 15 and Figures 5 and 6 ). Results for the 10 mg and 25 mg empagliflozin dosages were consistent with results for the combined dosage groups. Table 15Treatment Effect for the Primary Composite Endpoint and its Components a Placebo N=2,333 JARDIANCE N=4,687 Hazard ratio vs placebo (95% CI) a Treated set (patients who had received at least one dose of trial drug) b p-value for superiority (2-sided) 0.04 c Total number of events Composite of CV death, non-fatal myocardial infarction, non-fatal stroke (time to first occurrence) b 282 (12.1%) 490 (10.5%) 0.86 (0.74, 0.99) Non-fatal myocardial infarction c 121 (5.2%) 213 (4.5%) 0.87 (0.70, 1.09) Non-fatal stroke c 60 (2.6%) 150 (3.2%) 1.24 (0.92, 1.67) CV death c 137 (5.9%) 172 (3.7%) 0.62 (0.49, 0.77) Figure 5 Estimated Cumulative Incidence of First MACE Figure 6 Estimated Cumulative Incidence of CV Death The efficacy of JARDIANCE on CV death was generally consistent across major demographic and disease subgroups. Vital status was obtained for 99.2% of subjects in the trial. A total of 463 deaths were recorded during the EMPA-REG OUTCOME trial. Most of these deaths were categorized as CV deaths. The non-CV deaths were only a small proportion of deaths and were balanced between the treatment groups (2.1% in patients treated with JARDIANCE, and 2.4% of patients treated with placebo). Figure 5 Figure 6 14.4 Heart Failure Trials in Adults EMPEROR-Reduced (NCT03057977) was a double-blind trial conducted in adults with chronic heart failure (New York Heart Association [NYHA] functional class II-IV) with left ventricular ejection fraction (LVEF) ≤40% to evaluate the efficacy of JARDIANCE as adjunct to standard of care heart failure therapy. Of 3,730 patients, 1,863 were randomized to JARDIANCE 10 mg and 1,867 to placebo and were followed for a median of 16 months. The mean age of the trial population was 67 years (range: 25 to 94 years) and 76% were men, 24% were women, and 27% were 75 years of age or older. Approximately 71% of the trial population were White, 18% Asian, and 7% Black or African American. At baseline, 50% of the patients had type 2 diabetes mellitus.

16 months. The mean age of the trial population was 67 years (range: 25 to 94 years) and 76% were men, 24% were women, and 27% were 75 years of age or older. Approximately 71% of the trial population were White, 18% Asian, and 7% Black or African American. At baseline, 50% of the patients had type 2 diabetes mellitus. At randomization, 75% of patients were NYHA class II, 24% were class III, and 0.5% were class IV. The mean LVEF was 28%. At baseline, the mean eGFR was 62 mL/min/1.73 m 2 and the median urinary albumin to creatinine ratio (UACR) was 22 mg/g. Approximately half of the patients (52%) had eGFR equal to or above 60 mL/min/1.73 m 2 , 24% had eGFR 45 to less than 60 mL/min/1.73 m 2 , 19% had eGFR 30 to less than 45 mL/min/1.73 m 2 , and 5% had eGFR 20 to less than 30 mL/min/1.73 m 2 . At baseline, 88% of patients were treated with angiotensin-converting enzyme (ACE) inhibitors, angiotensin receptor blockers (ARB), or angiotensin receptor-neprilysin inhibitors (ARNI), 95% with beta-blockers, 71% with mineralocorticoid receptor antagonists (MRA), and 95% with diuretics. The primary endpoint was the time to first event of either cardiovascular (CV) death or hospitalization for heart failure (HHF). First and recurrent HHF was assessed as a key secondary endpoint. JARDIANCE was superior in reducing the risk of the primary composite endpoint of cardiovascular death or hospitalization for heart failure compared with placebo, mostly through a reduction in hospitalization for heart failure. JARDIANCE reduced the risk of first and recurrent HHF (see Table 16 and Figures 7 and 8 ). Table 16Treatment Effect for the Primary Composite Endpoint, its Components, and Key Secondary Endpoints Placebo N=1,867 JARDIANCE 10 mg N=1,863 Hazard ratio vs placebo (95% CI) p-value Number of Patients (%) a Time to first event b Includes deaths following hospitalization c Joint frailty model accounting for CV death CV death or HHF a 462 (24.7%) 361 (19.4%) 0.75 (0.65, 0.86) <0.0001 CV death a,b 202 (10.8%) 187 (10.0%) 0.92 (0.75, 1.12) HHF a 342 (18.3%) 246 (13.2%) 0.69 (0.59, 0.81) Number of Events First and recurrent HHF c 553 388 0.70 (0.58, 0.85) 0.0003 Figure 7 Time to First Occurrence of the Primary Composite Endpoint of CV Death or Hospitalization for Heart Failure Figure 8 Time to Event of Hospitalization for Heart Failure (First and Recurrent) The results of the primary composite were generally consistent across the pre-specified subgroups (see Figure 9 ). Figure 9 Treatment Effects for the Primary Composite Endpoint (CV Death and Hospitalization for Heart Failure) Subgroup Analysis (EMPEROR-Reduced) LVEF >30%: Includes both above and below the median NT-proBNP. To be eligible for inclusion, patients with an LVEF >30% were required to meet a higher NT-proBNP threshold than those with LVEF ≤30%, unless they additionally had a history of HHF within the past 12 months. EMPEROR-Preserved (NCT03057951) was a double-blind trial conducted in adults with chronic heart failure NYHA Class II-IV with LVEF >40% to evaluate the efficacy of JARDIANCE as adjunct to standard of care therapy. Of 5,988 patients, 2,997 were randomized to JARDIANCE 10 mg and 2,991 to placebo and were followed for a median of 26 months. The mean age of the trial population was 72 years (range: 22 to 100 years) and 55% were men, 45% were women, and 43% were 75 years of age or older. Approximately 76% of the trial population were White, 14% Asian, and 4% Black or African American. At randomization, 82% of patients were NYHA class II, 18% were class III, and 0.3% were class IV. The EMPEROR-Preserved trial population included patients with a LVEF <50% (33.1%), with a LVEF 50 to <60% (34.4%) and a LVEF ≥60% (32.5%).

6% of the trial population were White, 14% Asian, and 4% Black or African American. At randomization, 82% of patients were NYHA class II, 18% were class III, and 0.3% were class IV. The EMPEROR-Preserved trial population included patients with a LVEF <50% (33.1%), with a LVEF 50 to <60% (34.4%) and a LVEF ≥60% (32.5%). At baseline, the mean eGFR was 61 mL/min/1.73 m 2 and the median urinary albumin to creatinine ratio (UACR) was 21 mg/g. Approximately half of the patients (50%) had eGFR equal to or above 60 mL/min/1.73 m 2 , 26% had eGFR 45 to less than 60 mL/min/1.73 m 2 , 19% had eGFR 30 to less than 45 mL/min/1.73 m 2 , and 5% had eGFR 20 to less than 30 mL/min/1.73 m 2 . At baseline, 81% of patients were treated with ACE inhibitors, ARBs, or ARNI, 86% with beta-blockers, 38% with MRAs, and 86% with diuretics. The primary endpoint was the time to first event of either CV death or HHF. First and recurrent HHF was assessed as a key secondary endpoint. JARDIANCE was superior in reducing the risk of the primary composite endpoint compared with placebo, mostly through a reduction in hospitalization for heart failure. JARDIANCE reduced the risk of first and recurrent HHF (see Table 17 and Figures 10 and 11 ). Table 17Treatment Effect for the Primary Composite Endpoint, its Components, and Key Secondary Endpoints Placebo N=2,991 JARDIANCE 10 mg N=2,997 Hazard ratio vs placebo (95% CI) p-value Number of Patients (%) a Time to first event b Includes deaths following hospitalization c Joint frailty model accounting for CV death CV death or HHF a 511 (17.1%) 415 (13.8%) 0.79 (0.69, 0.90) 0.0003 CV death a,b 244 (8.2%) 219 (7.3%) 0.91 (0.76, 1.09) HHF a 352 (11.8%) 259 (8.6%) 0.71 (0.60, 0.83) Number of Events First and recurrent HHF c 541 407 0.73 (0.61, 0.88) 0.0009 Figure 10 Time to First Occurrence of the Primary Composite Endpoint of CV Death or Hospitalization for Heart Failure Figure 11 Time to Event of Hospitalization for Heart Failure (First and Recurrent) The results of the primary composite endpoint were consistent across the pre-specified subgroups (see Figure 12 ). Figure 12 Treatment Effects for the Primary Composite Endpoint (CV Death or Hospitalization for Heart Failure) Subgroup Analysis (EMPEROR-Preserved) Figure 7 Figure 8 Figure 9 Figure 10 Figure 11 Figure 12 14.5 Chronic Kidney Disease Trial in Adults EMPA-KIDNEY (NCT03594110) was a randomized, double-blind, placebo-controlled trial conducted in adults with chronic kidney disease (eGFR ≥20 to <45 mL/min/1.73 m 2 ; or eGFR ≥45 to <90 mL/min/1.73 m 2 with urine albumin to creatinine ratio [UACR] ≥200 mg/g). The trial excluded patients with polycystic kidney disease or patients requiring intravenous immunosuppressive therapy in the preceding three months or >45 mg of prednisone (or equivalent) at the time of screening. The primary objective of the trial was to assess the effects of empagliflozin as an adjunct to standard of care therapy, including RAS-inhibitor therapy when appropriate, on time to kidney disease progression or cardiovascular death. A total of 6,609 patients, were equally randomized to JARDIANCE 10 mg or placebo and were followed for a median of 24 months. The mean age of the study population was 63 years (range: 18 to 94 years) and 67% were male. Approximately 58% of the study population were White, 36% Asian, and 4% Black or African American. Approximately 44% of the patients had type 2 diabetes mellitus. At baseline, the mean eGFR was 37 mL/min/1.73 m 2 , 21% of patients had an eGFR equal to or above 45 mL/min/1.73 m 2 , 44% had an eGFR 30 to less than 45 mL/min/1.73 m 2 , and 35% had an eGFR less than 30 mL/min/1.73 m 2 . The median UACR was 329 mg/g, 20% of patients had a UACR <30 mg/g, 28% had a UACR 30 to ≤300mg/g, and 52% had a UACR >300 mg/g.

37 mL/min/1.73 m 2 , 21% of patients had an eGFR equal to or above 45 mL/min/1.73 m 2 , 44% had an eGFR 30 to less than 45 mL/min/1.73 m 2 , and 35% had an eGFR less than 30 mL/min/1.73 m 2 . The median UACR was 329 mg/g, 20% of patients had a UACR <30 mg/g, 28% had a UACR 30 to ≤300mg/g, and 52% had a UACR >300 mg/g. Approximately 1% of patients had type 1 diabetes at baseline. The most common etiologies of CKD were diabetic nephropathy/diabetic kidney disease (31%), glomerular disease (25%), hypertensive/renovascular disease (22%) and other/unknown (22%). At baseline, 85% of patients were treated with ACE inhibitor or ARB, 64% with statins, and 34% with antiplatelet agents. JARDIANCE was superior to placebo in reducing the risk of the primary composite endpoint of sustained ≥40% eGFR decline, sustained eGFR <10 mL/min/1.73 m 2 , progression to end-stage kidney disease, or CV or renal death. The treatment effect reflected a reduction in a sustained ≥40% eGFR decline, sustained eGFR <10 mL/min/1.73 m 2 , progression to end-stage kidney disease, and CV death. There were few renal deaths during the trial. JARDIANCE also reduced the risk of first and recurrent hospitalization (see Table 18 and Figure 13 ); information collected on the reason for hospitalization was insufficient to further characterize the benefit. Table 18Treatment Effect for the Primary Composite Endpoint, its Components and Key Secondary Endpoints Placebo N=3,305 JARDIANCE 10 mg N=3,304 Hazard ratio vs placebo (95% CI) p-value CV=Cardiovascular, eGFR=Estimated glomerular filtration rate, ESKD=End-stage kidney disease a ESKD is defined as the initiation of maintenance dialysis or receipt of a kidney transplant. b There were too few events of renal death to compute a reliable hazard ratio. c Information collected on the reason for hospitalization was insufficient to further characterize the benefit. Number of Patients (%) Composite of sustained ≥40% eGFR decline, sustained eGFR <10 mL/min/1.73 m 2 , ESKD a , or CV or renal death (time to first occurrence) 558 (16.9) 432 (13.1) 0.72 (0.64, 0.82) <0.0001 Sustained ≥40% eGFR decline 474 (14.3) 359 (10.9) 0.70 (0.61, 0.81) ESKD a or sustained eGFR <10 mL/min/1.73 m 2 221 (6.7) 157 (4.8) 0.69 (0.56, 0.84) Renal death b 4 (0.1) 4 (0.1) CV death 69 (2.1) 59 (1.8) 0.84 (0.60, 1.19) Number of Events First and recurrent hospitalization c 1,895 1,611 0.86 (0.78, 0.95) 0.0025 Figure 13 Time to First Occurrence of the Primary Composite Endpoint, Sustained ≥40% eGFR Decline, Sustained eGFR <10 mL/min/1.73 m 2 , ESKD or Renal Death, or CV Death The results of the primary composite endpoint were generally consistent across the pre-specified subgroups examined, including eGFR categories, underlying cause of kidney disease, diabetes status, or background use of RAS inhibitors (see Figure 14 ). The treatment benefit with JARDIANCE on the primary composite endpoint was not evident in patients with very low levels of albuminuria, however there were few events in these patients. Figure 14 Treatment Effects for the Primary Composite Endpoint (Sustained ≥40% eGFR Decline, Sustained eGFR <10 mL/min/1.73 m 2 , ESKD or Renal Death, or CV Death) Subgroup Analysis (EMPA-KIDNEY) *=Trend test Figure 13 Figure 14

<table ID="_Reftable5" width="75%"><caption>Table 5Results at Week 24 From a Placebo-Controlled Monotherapy Trial of JARDIANCE</caption><col width="36%"/><col width="19%"/><col width="19%"/><col width="14%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE</content> <content styleCode="bold">10 mg</content> <content styleCode="bold">N=224</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE</content> <content styleCode="bold">25 mg</content> <content styleCode="bold">N=224</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=228</content></th></tr></thead><tfoot><tr><td align="left" colspan="4" valign="top">^aModified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 9.4%, 9.4%, and 30.7% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA derived p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region.

rial (LOCF) was used to impute missing data at Week 24. At Week 24, 9.4%, 9.4%, and 30.7% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA derived p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) ^cFPG (mg/dL); for JARDIANCE 10 mg, n=223, for JARDIANCE 25 mg, n=223, and for placebo, n=226</td></tr></tfoot><tbody><tr><td colspan="4" styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="bold">HbA1c (%)^a</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>7.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>7.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>7.9</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.7</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.1</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (97.5% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.7^b (-0.9, -0.6)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.9^b (-1.0, -0.7)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Patients [n (%)] achieving HbA1c &lt;7%</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>72 (35%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>88 (44%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>25 (12%)</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">FPG (mg/dL)^c</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>153</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>153</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>155</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-19</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-25</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>12</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-31 (-37, -26)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-36 (-42, -31)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styl

aph>-31 (-37, -26)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-36 (-42, -31)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styl eCode="bold">Body Weight</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean) in kg</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>78</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>78</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>78</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> % change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-3.2</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.4</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.5^b (-3.1, -1.9)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.8^b (-3.4, -2.2)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr></tbody></table> <table ID="_Reffigure3" styleCode="Noautorules" width="75%"><caption>Figure 3 Adjusted Mean HbA1c Change at Each Time Point (Completers) and at Week 24 (mITT Population) - LOCF</caption><col width="87%"/><tbody><tr><td valign="top"><renderMultiMedia ID="id1946" referencedObject="MM4"/></td></tr></tbody></table>

eCode="bold">Body Weight</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean) in kg</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>78</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>78</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>78</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> % change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-3.2</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.4</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.5^b (-3.1, -1.9)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.8^b (-3.4, -2.2)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr></tbody></table> <table ID="_Reffigure3" styleCode="Noautorules" width="75%"><caption>Figure 3 Adjusted Mean HbA1c Change at Each Time Point (Completers) and at Week 24 (mITT Population) - LOCF</caption><col width="87%"/><tbody><tr><td valign="top"><renderMultiMedia ID="id1946" referencedObject="MM4"/></td></tr></tbody></table> <table ID="_Reftable6" width="75%"><caption>Table 6Results at Week 24 From a Placebo-Controlled Trial for JARDIANCE used in Combination with Metformin</caption><col width="36%"/><col width="19%"/><col width="19%"/><col width="14%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE</content> <content styleCode="bold">10 mg</content> <content styleCode="bold">N=217</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE</content> <content styleCode="bold">25 mg</content> <content styleCode="bold">N=213</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=207</content></th></tr></thead><tfoot><tr><td align="left" colspan="4" valign="top">^aModified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 9.7%, 14.1%, and 24.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region.

on on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 9.7%, 14.1%, and 24.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) ^cFPG (mg/dL); for JARDIANCE 10 mg, n=216, for JARDIANCE 25 mg, n=213, and for placebo, n=207</td></tr></tfoot><tbody><tr><td colspan="4" styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="bold">HbA1c (%)^a</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>7.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>7.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>7.9</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.7</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.1</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo + metformin (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.6^b (-0.7, -0.4)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.6^b (-0.8, -0.5)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Patients [n (%)] achieving HbA1c &lt;7%</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>75 (38%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>74 (39%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>23 (13%)</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">FPG (mg/dL)^c</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>155</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>149</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>156</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-20</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-22</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>6</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo + metformin (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-26</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-29</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bo

"top"><paragraph>-26</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-29</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bo ld">Body Weight</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline mean in kg</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>82</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>82</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>80</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> % change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.5</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.5</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.0^b (-2.6, -1.4)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.5^b (-3.1, -1.9)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr></tbody></table>

leCode="Rrule Botrule " valign="top"><paragraph>-2.0^b (-2.6, -1.4)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.5^b (-3.1, -1.9)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr></tbody></table> <table ID="_Reftable7" width="90%"><caption>Table 7Glycemic Parameters at 24 Weeks in a Trial Comparing JARDIANCE and Metformin to the Individual Components as Initial Therapy</caption><col width="11%"/><col width="12%"/><col width="12%"/><col width="12%"/><col width="12%"/><col width="12%"/><col width="12%"/><col width="10%"/><col width="10%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">10 mg + </content> <content styleCode="bold">Metformin </content> <content styleCode="bold">1,000 mg^a</content> <content styleCode="bold">N=161</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">10 mg + </content> <content styleCode="bold">Metformin </content> <content styleCode="bold">2,000 mg^a</content> <content styleCode="bold">N=167</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">25 mg + </content> <content styleCode="bold">Metformin </content> <content styleCode="bold">1,000 mg^a</content> <content styleCode="bold">N=165</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">25 mg + </content> <content styleCode="bold">Metformin </content> <content styleCode="bold">2,000 mg^a</content> <content styleCode="bold">N=169</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">10 mg </content> <content styleCode="bold">N=169</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">25 mg </content> <content styleCode="bold">N=163</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">Metformin </content> <content styleCode="bold">1,000 mg^a</content> <content styleCode="bold">N=167</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">Metformin </content> <content styleCode="bold">2,000 mg^a</content> <content styleCode="bold">N=162</content></th></tr></thead><tfoot><tr><td align="left" colspan="9" valign="top">^aMetformin total daily dose, administered in two equally divided doses per day. ^bp-value &#x2264;0.0062 (modified intent-to-treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c).

" colspan="9" valign="top">^aMetformin total daily dose, administered in two equally divided doses per day. ^bp-value &#x2264;0.0062 (modified intent-to-treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c). ^cp-value &#x2264;0.0056 (modified intent-to-treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c).</td></tr></tfoot><tbody><tr><td styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="bold">HbA1c (%)</content></paragraph></td><td styleCode="Rrule Toprule Botrule " valign="top"/><td styleCode="Rrule Toprule Botrule " valign="top"/><td styleCode="Rrule Toprule Botrule " valign="top"/><td styleCode="Rrule Toprule Botrule " valign="top"/><td styleCode="Rrule Toprule Botrule " valign="top"/><td styleCode="Rrule Toprule Botrule " valign="top"/><td styleCode="Rrule Toprule Botrule " valign="top"/><td styleCode="Rrule Toprule Botrule " valign="top"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.7</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.7</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.7</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.6</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.7</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.6</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-2.0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-2.1</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-1.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-2.1</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-1.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-1.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-1.2</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-1.8</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Comparison vs JARDIANCE (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.6^b (-0.9, -0.4)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.7^b (-1.0, -0.5)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.6^c (-0.8, -0.3)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.7^c (-1.0, -0.5)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td><td align="center" sty

eCode="bold">--</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td><td align="center" sty leCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph>Comparison vs metformin (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.8^b (-1.0, -0.6)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.3^b (-0.6, -0.1)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.8^c (-1.0, -0.5)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.3^c (-0.6, -0.1)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td></tr></tbody></table>

leCode="bold">--</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">--</content></paragraph></td></tr></tbody></table> <table ID="_Reftable8" width="75%"><caption>Table 8Results at Week 24 from a Placebo-Controlled Trial for JARDIANCE in Combination with Metformin and Sulfonylurea</caption><col width="36%"/><col width="19%"/><col width="19%"/><col width="14%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">10 mg</content> <content styleCode="bold">N=225</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">25 mg</content> <content styleCode="bold">N=216</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=225</content></th></tr></thead><tfoot><tr><td align="left" colspan="4" valign="top">^aModified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 17.8%, 16.7%, and 25.3% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region.

n on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 17.8%, 16.7%, and 25.3% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) ^cFPG (mg/dL); for JARDIANCE 10 mg, n=225, for JARDIANCE 25 mg, n=215, for placebo, n=224</td></tr></tfoot><tbody><tr><td colspan="4" styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="bold">HbA1c (%)^a</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.1</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.1</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.2</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.2</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.6^b (-0.8, -0.5)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.6^b (-0.7, -0.4)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Patients [n (%)] achieving HbA1c &lt;7%</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>55 (26%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>65 (32%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>20 (9%)</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">FPG (mg/dL)^c</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>151</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>156</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>152</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-23</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-23</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>6</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-29</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-29</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">Body Weight</content></pa

ph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-29</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">Body Weight</content></pa ragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline mean in kg</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>77</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>78</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>76</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> % change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-3.2</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.5</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.4^b (-3.0, -1.8)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.7^b (-3.3, -2.1)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr></tbody></table>

leCode="Rrule Botrule " valign="top"><paragraph>-2.4^b (-3.0, -1.8)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.7^b (-3.3, -2.1)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr></tbody></table> <table ID="_Reftable9" width="75%"><caption>Table 9Results at Week 52 from an Active-Controlled Trial Comparing JARDIANCE to Glimepiride as Add-On Therapy in Patients Inadequately Controlled on Metformin</caption><col width="49%"/><col width="19%"/><col width="19%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE 25 mg</content> <content styleCode="bold">N=765</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">Glimepiride</content> <content styleCode="bold">N=780</content></th></tr></thead><tfoot><tr><td align="left" colspan="3" valign="top">^aModified intent-to-treat population. Last observation on trial (LOCF) was used to impute data missing at Week 52. At Week 52, data was imputed for 15.3% and 21.9% of patients randomized to JARDIANCE 25 mg and glimepiride, respectively.

t></th></tr></thead><tfoot><tr><td align="left" colspan="3" valign="top">^aModified intent-to-treat population. Last observation on trial (LOCF) was used to impute data missing at Week 52. At Week 52, data was imputed for 15.3% and 21.9% of patients randomized to JARDIANCE 25 mg and glimepiride, respectively. ^bNon-inferior, ANCOVA model p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region) ^cANCOVA p-value &lt;0.0001 (Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) ^dFPG (mg/dL); for JARDIANCE 25 mg, n=764, for glimepiride, n=779</td></tr></tfoot><tbody><tr><td colspan="3" styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="bold">HbA1c (%)^a</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>7.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>7.9</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.7</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.7</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from glimepiride (adjusted mean) (97.5% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.07^b (-0.15, 0.01)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td colspan="3" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">FPG (mg/dL)^d</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>150</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>150</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-19</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-9</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from glimepiride (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-11</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td colspan="3" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">Body Weight</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline mean in kg</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>82.5</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>83</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> % change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-3.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>2.0</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from glimepiride (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><

aragraph>-3.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>2.0</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from glimepiride (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top">< paragraph>-5.9^c (-6.3, -5.5)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr></tbody></table> <table ID="_Reffigure4" styleCode="Noautorules" width="75%"><caption>Figure 4 Adjusted mean HbA1c Change at Each Time Point (Completers) and at Week 52 (mITT Population) - LOCF</caption><col width="87%"/><tbody><tr><td valign="top"><renderMultiMedia ID="id2415" referencedObject="MM5"/></td></tr></tbody></table> <table ID="_Reftable10" width="75%"><caption>Table 10Results of Placebo-Controlled Trial for JARDIANCE in Combination Therapy with Pioglitazone</caption><col width="32%"/><col width="19%"/><col width="19%"/><col width="17%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">10 mg</content> <content styleCode="bold">N=165</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">25 mg</content> <content styleCode="bold">N=168</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=165</content></th></tr></thead><tfoot><tr><td align="left" colspan="4" valign="top">^aModified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 10.9%, 8.3%, and 20.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and background medication.

CF) was used to impute missing data at Week 24. At Week 24, 10.9%, 8.3%, and 20.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and background medication. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) ^cFPG (mg/dL); for JARDIANCE 10 mg, n=163</td></tr></tfoot><tbody><tr><td colspan="4" styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="bold">HbA1c (%)^a</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.1</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.1</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.2</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.6</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.7</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.1</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo + pioglitazone (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.5^b (-0.7, -0.3)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.6^b (-0.8, -0.4)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Patients [n (%)] achieving HbA1c &lt;7%</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>36 (24%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>48 (30%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>12 (8%)</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">FPG (mg/dL)^c</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>152</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>152</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>152</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-17</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-22</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>7</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo + pioglitazone (adjusted mean) (97.5% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-23^b (-31.8, -15.2)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-28^b (-36.7, -20.2)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="to

>b</sup> (-31.8, -15.2)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-28^b (-36.7, -20.2)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr><tr><td colspan="4" styleCode="Rrule Lrule Botrule " valign="to p"><paragraph><content styleCode="bold">Body Weight</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline mean in kg</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>78</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>79</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>78</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> % change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-2.0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-1.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.6</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-2.6^b (-3.4, -1.8)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-2.4^b (-3.2, -1.6)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr></tbody></table>

rule Botrule " valign="middle"><paragraph>-2.6^b (-3.4, -1.8)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-2.4^b (-3.2, -1.6)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr></tbody></table> <table ID="_Reftable11" width="90%"><caption>Table 11Results at Week 18 and 78 for a Placebo-Controlled Trial for JARDIANCE in Combination with Insulin</caption><col width="15%"/><col width="15%"/><col width="15%"/><col width="12%"/><col width="15%"/><col width="15%"/><col width="12%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" colspan="3" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">18 weeks</content> <content styleCode="bold">(no insulin adjustment)</content></th><th align="center" colspan="3" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">78 weeks</content> <content styleCode="bold">(adjustable insulin dose after 18 weeks)</content></th></tr><tr><th align="left" styleCode="Rrule Lrule Botrule " valign="top"/><th align="center" styleCode="Rrule Botrule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">10 mg</content> <content styleCode="bold">N=169</content></th><th align="center" styleCode="Rrule Botrule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">25 mg</content> <content styleCode="bold">N=155</content></th><th align="center" styleCode="Rrule Botrule " valign="top"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=170</content></th><th align="center" styleCode="Rrule Botrule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">10 mg</content> <content styleCode="bold">N=169</content></th><th align="center" styleCode="Rrule Botrule " valign="top"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">25 mg</content> <content styleCode="bold">N=155</content></th><th align="center" styleCode="Rrule Botrule " valign="top"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=170</content></th></tr></thead><tfoot><tr><td align="left" colspan="7" valign="top">^aModified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 18 and 78. At Week 18, 21.3%, 30.3%, and 21.8% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. At Week 78, 32.5%, 38.1% and 42.4% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, and region; FPG: MMRM model includes baseline FPG, baseline HbA1c, treatment, region, visit and visit by treatment interaction. Body weight: MMRM model includes baseline body weight, baseline HbA1c, treatment, region, visit and visit by treatment interaction.

001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, and region; FPG: MMRM model includes baseline FPG, baseline HbA1c, treatment, region, visit and visit by treatment interaction. Body weight: MMRM model includes baseline body weight, baseline HbA1c, treatment, region, visit and visit by treatment interaction. ^cp-value=0.0049 ^dp-value=0.0052 ^ep-value=0.0463</td></tr></tfoot><tbody><tr><td colspan="7" styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="bold">HbA1c (%)^a</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.3</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.3</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.2</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.3</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.3</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.2</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.6</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.7</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.6</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.1</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (97.5% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.6^b (-0.8, -0.4)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.7^b (-0.9, -0.5)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.5^b (-0.7, -0.3)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.7^b (-0.9, -0.5)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Patients (%) achieving HbA1c &lt;7%</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>18.0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>19.5</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>5.5</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>12.0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>17.5</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>6.7</paragraph></td></tr><tr><td colspan="7" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">FPG (mg/dL)</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>138</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>146</paragraph></

">FPG (mg/dL)</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>138</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>146</paragraph></ td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>142</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>138</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>146</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>142</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean, SE)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-17.9 (3.2)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-19.1 (3.3)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>10.4 (3.1)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-10.1 (3.2)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-15.2 (3.4)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>2.8 (3.2)</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-28.2^b (-37.0, -19.5)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-29.5^b (-38.4, -20.6)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-12.9^c (-21.9, 3.9)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-17.9^b (-27.0, -8.8)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr><tr><td colspan="7" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">Body Weight</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline mean in kg</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>92</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>95</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>90</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>92</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>95</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>90</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> % change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-1.8</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-1.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.1</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-2.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-2.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.7</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</para

ph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-2.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.7</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</para graph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-1.7^d (-3.0, -0.5)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-1.3^e (-2.5, -0.0)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-3.0^b (-4.4, -1.7)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-3.0^b (-4.4, -1.6)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr></tbody></table>

rule Botrule " valign="middle"><paragraph>-3.0^b (-4.4, -1.7)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-3.0^b (-4.4, -1.6)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr></tbody></table> <table ID="_Reftable12" width="75%"><caption>Table 12Results at Week 18 for a Placebo-Controlled Trial for JARDIANCE in Combination with Insulin and with or without Metformin</caption><col width="32%"/><col width="19%"/><col width="19%"/><col width="17%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE 10 mg</content> <content styleCode="bold">N=186</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE 25 mg</content> <content styleCode="bold">N=189</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=188</content></th></tr></thead><tfoot><tr><td align="left" colspan="4" valign="top">^aModified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 18. At Week 18, 23.7%, 22.8% and 23.4% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, geographical region, and background medication).</td></tr></tfoot><tbody><tr><td colspan="4" styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="bold">HbA1c (%)^a</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.4</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.3</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.3</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline (adjusted mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.9</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-1.0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.5</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.4^b (-0.6, -0.3)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.5^b (-0.7, -0.4)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr></tbody></table>

rule Botrule " valign="middle"><paragraph>-0.4^b (-0.6, -0.3)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>-0.5^b (-0.7, -0.4)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>--</paragraph></td></tr></tbody></table> <table ID="_Reftable13" width="75%"><caption>Table 13Results at Week 24 (LOCF) of Placebo-Controlled Trial for JARDIANCE in Adults with Type 2 Diabetes Mellitus and Renal Impairment</caption><col width="43%"/><col width="43%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">Mild and Moderate Impairment^b</content></th></tr><tr><th align="left" styleCode="Rrule Lrule Botrule " valign="top"/><th align="center" styleCode="Rrule Botrule " valign="top"><content styleCode="bold">JARDIANCE 25 mg</content></th></tr></thead><tfoot><tr><td align="left" colspan="2" valign="top">^ap-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and background medication) ^beGFR 30 to less than 90 mL/min/1.73 m² - Modified intent-to-treat population. Last observation on trial (LOCF) was used to impute missing data at Week 24. At Week 24, 24.6% and 26.2% was imputed for patients randomized to JARDIANCE 25 mg and placebo, respectively.</td></tr></tfoot><tbody><tr><td styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="bold">HbA1c</content></paragraph></td><td styleCode="Rrule Toprule Botrule " valign="top"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Number of patients</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>n=284</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Comparison vs placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.5^a (-0.6, -0.4)</paragraph></td></tr></tbody></table>

" valign="top"><paragraph>n=284</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Comparison vs placebo (adjusted mean) (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.5^a (-0.6, -0.4)</paragraph></td></tr></tbody></table> <table ID="_Reftable14" width="90%"><caption>Table 14Results at Week 26 for a Placebo-Controlled Trial for JARDIANCE in Combination with Metformin and/or Insulin or as Monotherapy in Pediatric Patients Aged 10 to 17 Years with Type 2 Diabetes Mellitus^a</caption><col width="60%"/><col width="20%"/><col width="20%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE</content> <content styleCode="bold">10 mg and 25 mg</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">Placebo</content></th></tr></thead><tfoot><tr><td align="left" colspan="3" valign="top">^aModified intent-to-treat set (All randomized and treated patients with baseline measurement). ^bMultiple imputations using placebo wash-out approach with 500 iterations for missing data. Imputed for HbA1c (Jardiance N=5 (9.6 %), Placebo N=3 (5.7%)), for FPG (Jardiance N=4 (8.3%), Placebo N=2 (3.8%)). ^cLeast-Square Mean from Analysis of Covariance (ANCOVA) adjusted for baseline value and baseline age stratum (&lt; 15 years vs 15 to &lt; 18 years). ^dNot evaluated for statistical significance, not part of sequential testing procedure.

3 (5.7%)), for FPG (Jardiance N=4 (8.3%), Placebo N=2 (3.8%)). ^cLeast-Square Mean from Analysis of Covariance (ANCOVA) adjusted for baseline value and baseline age stratum (&lt; 15 years vs 15 to &lt; 18 years). ^dNot evaluated for statistical significance, not part of sequential testing procedure. ^ep-value=0.0116 (two-sided)</td></tr></tfoot><tbody><tr><td colspan="3" styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph><content styleCode="bold">HbA1c (%)^b</content></paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Number of patients</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>n=52</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>n=53</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.0</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>8.1</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.2</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>0.7</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Difference from placebo^c (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-0.8^e (-1.5, -0.2)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">FPG (mg/dL)^b,d</content></paragraph></td><td styleCode="Rrule Botrule " valign="top"/><td styleCode="Rrule Botrule " valign="top"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Number of patients</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>n=48</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>n=52</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Baseline (mean)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>154</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>159</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph> Change from baseline^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-19</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>17</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph> Difference from placebo^c (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-36 (-60.7, -10.7)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr></tbody></table>

le Botrule Lrule " valign="top"><paragraph> Difference from placebo^c (95% CI)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>-36 (-60.7, -10.7)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="top"><paragraph>--</paragraph></td></tr></tbody></table> <table ID="_Reftable15" width="75%"><caption>Table 15Treatment Effect for the Primary Composite Endpoint and its Components^a</caption><col width="33%"/><col width="17%"/><col width="19%"/><col width="17%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">Placebo </content> <content styleCode="bold">N=2,333</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">JARDIANCE </content> <content styleCode="bold">N=4,687</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">Hazard ratio vs placebo </content> <content styleCode="bold">(95% CI)</content></th></tr></thead><tfoot><tr><td align="left" colspan="4" valign="top">^aTreated set (patients who had received at least one dose of trial drug) ^bp-value for superiority (2-sided) 0.04 ^cTotal number of events</td></tr></tfoot><tbody><tr><td styleCode="Rrule Lrule Toprule Botrule " valign="top"><paragraph>Composite of CV death, non-fatal myocardial infarction, non-fatal stroke (time to first occurrence)^b</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>282 (12.1%)</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>490 (10.5%)</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>0.86 (0.74, 0.99)</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Non-fatal myocardial infarction^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>121 (5.2%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>213 (4.5%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.87 (0.70, 1.09)</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="top"><paragraph>Non-fatal stroke^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>60 (2.6%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>150 (3.2%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>1.24 (0.92, 1.67)</paragraph></td></tr><tr><td styleCode="Rrule Botrule Lrule " valign="top"><paragraph>CV death^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>137 (5.9%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>172 (3.7%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.62 (0.49, 0.77)</paragraph></td></tr></tbody></table>

n="center" styleCode="Rrule Botrule " valign="middle"><paragraph>137 (5.9%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>172 (3.7%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.62 (0.49, 0.77)</paragraph></td></tr></tbody></table> <table ID="_Reffigure5" styleCode="Noautorules" width="75%"><caption>Figure 5 Estimated Cumulative Incidence of First MACE</caption><col width="87%"/><tbody><tr><td valign="top"><renderMultiMedia ID="id2990" referencedObject="MM6"/></td></tr></tbody></table> <table ID="_Reffigure6" styleCode="Noautorules" width="75%"><caption>Figure 6 Estimated Cumulative Incidence of CV Death</caption><col width="87%"/><tbody><tr><td valign="top"><renderMultiMedia ID="id2997" referencedObject="MM7"/></td></tr></tbody></table>

<table ID="_Reffigure5" styleCode="Noautorules" width="75%"><caption>Figure 5 Estimated Cumulative Incidence of First MACE</caption><col width="87%"/><tbody><tr><td valign="top"><renderMultiMedia ID="id2990" referencedObject="MM6"/></td></tr></tbody></table> <table ID="_Reffigure6" styleCode="Noautorules" width="75%"><caption>Figure 6 Estimated Cumulative Incidence of CV Death</caption><col width="87%"/><tbody><tr><td valign="top"><renderMultiMedia ID="id2997" referencedObject="MM7"/></td></tr></tbody></table> <table ID="_RefTable16" width="85%"><caption>Table 16Treatment Effect for the Primary Composite Endpoint, its Components, and Key Secondary Endpoints</caption><col width="31%"/><col width="17%"/><col width="17%"/><col width="17%"/><col width="17%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="middle"/><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=1,867</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE 10 mg</content> <content styleCode="bold">N=1,863</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">Hazard ratio vs placebo</content> <content styleCode="bold">(95% CI)</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">p-value</content></th></tr><tr><th align="left" rowspan="1" styleCode="Rrule Lrule Botrule " valign="middle"/><th align="center" colspan="2" styleCode="Rrule Botrule " valign="middle"><content styleCode="bold">Number of Patients (%)</content></th><th align="left" colspan="2" styleCode="Rrule Botrule " valign="middle"/></tr></thead><tfoot><tr><td align="left" colspan="5" valign="top">^aTime to first event ^bIncludes deaths following hospitalization ^cJoint frailty model accounting for CV death</td></tr></tfoot><tbody><tr><td styleCode="Rrule Lrule Toprule Botrule " valign="middle"><paragraph>CV death or HHF^a</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>462 (24.7%)</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>361 (19.4%)</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>0.75 (0.65, 0.86)</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>&lt;0.0001</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"><paragraph>CV death^a,b</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>202 (10.8%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>187 (10.0%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.92 (0.75, 1.12)</paragraph></td><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"><paragraph>HHF^a</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>342 (18.3%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>246 (13.2%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.69 (0.59, 0.81)</paragraph></td><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"/><td align="center" colspan="2" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">Number of Events</content></paragraph></td><td styleCode="Rrule Botrule " valign="middle"/><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Botrule Lrule Toprule " valign="middle"><paragraph>First and recurrent HHF^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>553<

aragraph></td><td styleCode="Rrule Botrule " valign="middle"/><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Botrule Lrule Toprule " valign="middle"><paragraph>First and recurrent HHF^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>553< /paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>388</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.70 (0.58, 0.85)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.0003</paragraph></td></tr></tbody></table>

td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>388</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.70 (0.58, 0.85)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.0003</paragraph></td></tr></tbody></table> <table ID="_RefTable17" width="85%"><caption>Table 17Treatment Effect for the Primary Composite Endpoint, its Components, and Key Secondary Endpoints</caption><col width="31%"/><col width="17%"/><col width="17%"/><col width="17%"/><col width="17%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="middle"/><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=2,991</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">JARDIANCE 10 mg</content> <content styleCode="bold">N=2,997</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">Hazard ratio vs placebo</content> <content styleCode="bold">(95% CI)</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="top"><content styleCode="bold">p-value</content></th></tr><tr><th align="left" rowspan="1" styleCode="Rrule Lrule Botrule " valign="middle"/><th align="center" colspan="2" styleCode="Rrule Botrule " valign="middle"><content styleCode="bold">Number of Patients (%)</content></th><th align="left" colspan="2" styleCode="Rrule Botrule " valign="middle"/></tr></thead><tfoot><tr><td align="left" colspan="5" valign="top">^aTime to first event ^bIncludes deaths following hospitalization ^cJoint frailty model accounting for CV death</td></tr></tfoot><tbody><tr><td styleCode="Rrule Lrule Toprule Botrule " valign="middle"><paragraph>CV death or HHF^a</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>511 (17.1%)</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>415 (13.8%)</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>0.79 (0.69, 0.90)</paragraph></td><td align="center" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph>0.0003</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"><paragraph>CV death^a,b</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>244 (8.2%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>219 (7.3%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.91 (0.76, 1.09)</paragraph></td><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"><paragraph>HHF^a</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>352 (11.8%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>259 (8.6%)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.71 (0.60, 0.83)</paragraph></td><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"/><td align="center" colspan="2" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">Number of Events</content></paragraph></td><td styleCode="Rrule Botrule " valign="middle"/><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Botrule Lrule Toprule " valign="middle"><paragraph>First and recurrent HHF^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>541</paragr

h></td><td styleCode="Rrule Botrule " valign="middle"/><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Botrule Lrule Toprule " valign="middle"><paragraph>First and recurrent HHF^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>541</paragr aph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>407</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.73 (0.61, 0.88)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.0009</paragraph></td></tr></tbody></table>

td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>407</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.73 (0.61, 0.88)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.0009</paragraph></td></tr></tbody></table> <table ID="_RefTable18" width="85%"><caption>Table 18Treatment Effect for the Primary Composite Endpoint, its Components and Key Secondary Endpoints</caption><col width="30%"/><col width="17%"/><col width="18%"/><col width="17%"/><col width="17%"/><thead><tr><th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="middle"/><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">Placebo</content> <content styleCode="bold"> N=3,305</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">JARDIANCE 10 mg</content> <content styleCode="bold"> N=3,304</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">Hazard ratio vs placebo</content> <content styleCode="bold"> (95% CI)</content></th><th align="center" styleCode="Rrule Botrule Toprule " valign="middle"><content styleCode="bold">p-value</content></th></tr></thead><tfoot><tr><td align="left" colspan="5" valign="top">CV=Cardiovascular, eGFR=Estimated glomerular filtration rate, ESKD=End-stage kidney disease</td></tr><tr><td align="left" colspan="5" valign="top">^aESKD is defined as the initiation of maintenance dialysis or receipt of a kidney transplant.</td></tr><tr><td align="left" colspan="5" valign="top">^bThere were too few events of renal death to compute a reliable hazard ratio.</td></tr><tr><td align="left" colspan="5" valign="top">^cInformation collected on the reason for hospitalization was insufficient to further characterize the benefit.</td></tr></tfoot><tbody><tr><td styleCode="Rrule Lrule Toprule Botrule " valign="middle"/><td align="center" colspan="2" styleCode="Rrule Toprule Botrule " valign="middle"><paragraph><content styleCode="bold">Number of Patients (%)</content></paragraph></td><td styleCode="Rrule Toprule Botrule " valign="middle"/><td styleCode="Rrule Toprule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"><paragraph>Composite of sustained &#x2265;40% eGFR decline, sustained eGFR &lt;10 mL/min/1.73 m², ESKD^a, or CV or renal death (time to first occurrence)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>558 (16.9)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>432 (13.1)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.72 (0.64, 0.82)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>&lt;0.0001</paragraph></td></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"><paragraph> Sustained &#x2265;40% eGFR decline</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>474 (14.3)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>359 (10.9)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.70 (0.61, 0.81)</paragraph></td><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"><paragraph> ESKD^a or sustained eGFR &lt;10 mL/min/1.73 m²</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>221 (6.7)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>157 (4.8)</paragraph></td><td align="center" styleCode=

ragraph> ESKD^a or sustained eGFR &lt;10 mL/min/1.73 m²</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>221 (6.7)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>157 (4.8)</paragraph></td><td align="center" styleCode= "Rrule Botrule " valign="middle"><paragraph>0.69 (0.56, 0.84)</paragraph></td><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"><paragraph> Renal death^b</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>4 (0.1)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>4 (0.1)</paragraph></td><td styleCode="Rrule Botrule " valign="middle"/><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"><paragraph> CV death</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>69 (2.1)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>59 (1.8)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.84 (0.60, 1.19)</paragraph></td><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Lrule Botrule " valign="middle"/><td align="center" colspan="2" styleCode="Rrule Botrule " valign="middle"><paragraph><content styleCode="bold">Number of Events</content></paragraph></td><td styleCode="Rrule Botrule " valign="middle"/><td styleCode="Rrule Botrule " valign="middle"/></tr><tr><td styleCode="Rrule Botrule Lrule Toprule " valign="middle"><paragraph>First and recurrent hospitalization ^c</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>1,895</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>1,611</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.86 (0.78, 0.95)</paragraph></td><td align="center" styleCode="Rrule Botrule " valign="middle"><paragraph>0.0025</paragraph></td></tr></tbody></table>

16 HOW SUPPLIED/STORAGE AND HANDLING JARDIANCE tablets are available as follows: 10 mg tablets: pale yellow, round, biconvex, and bevel-edged film-coated tablets debossed with "S 10" on one side and the Boehringer Ingelheim company symbol on the other side. Bottles of approximately 720 film-coated tablets, NDC 55154-0411-8 25 mg tablets: pale yellow, oval, biconvex film-coated tablets, debossed with "S 25" on one side and the Boehringer Ingelheim company symbol on the other side. Bottles of approximately 990 film-coated tablets, NDC 55154-0412-8 Dispense in a well-closed container as defined in the USP. Storage Store at 20°C to 25°C (68°F to 77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [see USP Controlled Room Temperature].

17 PATIENT COUNSELING INFORMATION Advise the patient to read the FDA-approved patient labeling (Medication Guide). Diabetic Ketoacidosis in Patients with Type 1 Diabetes Mellitus and Other Ketoacidosis In patients with type 1 diabetes mellitus, inform them that using JARDIANCE can increase their risk of life-threatening diabetic ketoacidosis and that fatal ketoacidosis has occurred. For all other patients, inform them that JARDIANCE can cause potentially fatal ketoacidosis and that type 2 diabetes mellitus and pancreatic disorders (e.g., history of pancreatitis or pancreatic surgery) are risk factors. Educate all patients on precipitating factors (such as insulin dose reduction or missed insulin doses, infection, reduced caloric intake, ketogenic diet, surgery, dehydration, and alcohol abuse) and symptoms of ketoacidosis (including nausea, vomiting, abdominal pain, tiredness, and labored breathing). Inform patients that blood glucose may be normal even in the presence of ketoacidosis. Advise patients that they may be asked to monitor ketones. If symptoms of ketoacidosis occur, instruct patients to discontinue JARDIANCE and seek medical attention immediately [see Warnings and Precautions (5.1) ] . Volume Depletion Inform patients that symptomatic hypotension may occur with JARDIANCE and advise them to contact their healthcare provider if they experience such symptoms [see Warnings and Precautions (5.2) ] . Inform patients that dehydration may increase the risk for hypotension, and to maintain adequate fluid intake. Genitourinary Infections, including Urosepsis, Pyelonephritis, Necrotizing Fasciitis of the Perineum (Fournier's Gangrene), and Genital Mycotic Infections Counsel patients that genitourinary infections may occur when taking JARDIANCE and may become serious. Educate them on the symptoms and advise them to seek medical advice if symptoms occur. Specifically, advise patients to promptly seek medical attention if they develop pain or tenderness, redness, or swelling of the genitals or the area from the genitals back to the rectum, along with a fever above 100.4°F or malaise [see Warnings and Precautions (5.3) ] . Hypoglycemia Inform patients that hypoglycemia has been reported when JARDIANCE is used with insulin secretagogues or insulin. Hypoglycemia may occur in pediatric patients regardless of concomitant antidiabetic treatment. Educate patients or caregivers on the signs and symptoms of hypoglycemia [see Warnings and Precautions (5.4) ] . Lower Limb Amputation Counsel patients about the importance of routine preventative foot care. Instruct patients to monitor for new pain or tenderness, sores or ulcers, or infections involving the leg or foot and to seek medical advice immediately if such signs or symptoms develop [see Warnings and Precautions (5.5) ] . Hypersensitivity Reactions Inform patients that serious hypersensitivity reactions, such as urticaria and angioedema, have been reported with JARDIANCE. Advise patients to report immediately any skin reaction or angioedema, and to discontinue drug until they have consulted prescribing healthcare provider [see Warnings and Precautions (5.6) ] . Laboratory Tests Inform patients that elevated glucose in urinalysis is expected when taking JARDIANCE [see Drug Interactions (7) ] . Pregnancy Advise pregnant patients, and patients of reproductive potential, of the potential risk to a fetus with treatment with JARDIANCE [see Use in Specific Populations (8.1) ] .

] . Laboratory Tests Inform patients that elevated glucose in urinalysis is expected when taking JARDIANCE [see Drug Interactions (7) ] . Pregnancy Advise pregnant patients, and patients of reproductive potential, of the potential risk to a fetus with treatment with JARDIANCE [see Use in Specific Populations (8.1) ] . Instruct patients to report pregnancies to their healthcare provider as soon as possible. Lactation Advise patients that breastfeeding is not recommended during treatment with JARDIANCE [see Use in Specific Populations (8.2) ]. Missed Dose Instruct patients to take JARDIANCE only as prescribed. If a dose is missed, it should be taken as soon as the patient remembers. Advise patients not to double their next dose [see Dosage and Administration (2.4) ] .

Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877 USA Licensed from: Boehringer Ingelheim International GmbH, Ingelheim, Germany JARDIANCE is a registered trademark of and used under license from Boehringer Ingelheim International GmbH. Boehringer Ingelheim Pharmaceuticals, Inc. either owns or uses the EMPA-REG OUTCOME ® , EMPEROR-Reduced ® , EMPEROR-Preserved ® , and EMPA-KIDNEY ® trademarks under license. The other brands listed are trademarks of their respective owners and are not trademarks of Boehringer Ingelheim Pharmaceuticals, Inc. Copyright © 2026 Boehringer Ingelheim International GmbH ALL RIGHTS RESERVED Distributed By: Cardinal Health Dublin, OH 43017 ER7381I Rev. C ER7383 Rev. B COL8914QA062026 SPL14754C

MEDICATION GUIDE JARDIANCE ® (jar DEE ans) (empagliflozin tablets) for oral use What is the most important information I should know about JARDIANCE? JARDIANCE can cause serious side effects, including: • Diabetic ketoacidosis (increased ketones in your blood or urine) in people with type 1 and other ketoacidosis. JARDIANCE can cause ketoacidosis that can be life-threatening and may lead to death. Ketoacidosis is a serious condition which needs to be treated in a hospital. People with type 1 diabetes have a high risk of getting ketoacidosis. People with type 2 diabetes or pancreas problems also have an increased risk of getting ketoacidosis. Ketoacidosis can also happen in people who: are sick, cannot eat or drink as usual, skip meals, are on a diet high in fat and low in carbohydrates (ketogenic diet), take less than the usual amount of insulin or miss insulin doses, drink too much alcohol, have a loss of too much fluid from the body (volume depletion), or who have surgery. Ketoacidosis can happen even if your blood sugar is less than 250 mg/dL. Your healthcare provider may ask you to periodically check ketones in your urine or blood. Stop taking JARDIANCE and call your healthcare provider or get medical help right away if you get any of the following. If possible, check for ketones in your urine or blood, even if your blood sugar is less than 250 mg/dL: o nausea o vomiting o stomach-area (abdominal) pain o tiredness o trouble breathing o ketones in your urine or blood • Dehydration. JARDIANCE can cause some people to become dehydrated (the loss of body water and salt). Dehydration may cause you to feel dizzy, faint, light-headed, or weak, especially when you stand up (orthostatic hypotension). There have been reports of sudden worsening of kidney function in people who are taking JARDIANCE. You may be at higher risk of dehydration if you: o take medicines to lower your blood pressure, including diuretics (water pills) o are on low sodium (salt) diet o have kidney problems o are 65 years of age or older Talk to your healthcare provider about what you can do to prevent dehydration including how much fluid you should drink on a daily basis. Call your healthcare provider right away if you reduce the amount of food or liquid you drink, for example if you are sick or you cannot eat, or start to lose liquids from your body, for example from vomiting, diarrhea or being in the sun too long. What is JARDIANCE? JARDIANCE is a prescription medicine used to: o reduce the risk of cardiovascular death and hospitalization for heart failure in adults with heart failure, when the heart cannot pump enough blood to the rest of your body. o reduce the risk of further worsening of kidney disease, end-stage kidney disease (ESKD), death due to cardiovascular disease, and hospitalization in adults with chronic kidney disease. o reduce the risk of cardiovascular death in adults with type 2 diabetes and who also have known cardiovascular disease. o lower blood sugar (glucose) along with diet and exercise in adults and children who are 10 years of age and older with type 2 diabetes. JARDIANCE is not for use to lower blood sugar (glucose) in people with type 1 diabetes. It may increase their risk of diabetic ketoacidosis (increased ketones in blood or urine). JARDIANCE is not for use to lower blood sugar (glucose) in people with type 2 diabetes who have severe kidney problems, because it may not work.

DIANCE is not for use to lower blood sugar (glucose) in people with type 1 diabetes. It may increase their risk of diabetic ketoacidosis (increased ketones in blood or urine). JARDIANCE is not for use to lower blood sugar (glucose) in people with type 2 diabetes who have severe kidney problems, because it may not work. JARDIANCE is not for people with polycystic kidney disease, or who are taking or have recently received certain types of immunosuppressive therapy to treat kidney disease. JARDIANCE is not expected to work if you have these conditions. It is not known if JARDIANCE is safe and effective in children under 10 years of age. Who should not take JARDIANCE? Do not take JARDIANCE if you: • are allergic to empagliflozin or any of the ingredients in JARDIANCE. See the end of this Medication Guide for a complete list of ingredients in JARDIANCE. Symptoms of a serious allergic reaction to JARDIANCE may include: o rash o raised, red areas on your skin (hives) o swelling of your face, lips, mouth, and throat that may cause difficulty in breathing or swallowing If you have any of these symptoms, stop taking JARDIANCE and call your healthcare provider right away or go to the nearest hospital emergency room. What should I tell my healthcare provider before taking JARDIANCE? Before taking JARDIANCE, tell your healthcare provider about all of your medical conditions, including if you: • have type 1 diabetes or have had diabetic ketoacidosis. • have a decrease in your insulin dose. • have a serious infection. • have a history of infection of the vagina or penis. • have a history of amputation. • have kidney problems. • have liver problems. • have a history of urinary tract infections or problems with urination. • are on a low sodium (salt) diet. Your healthcare provider may change your diet or your dose. • are going to have surgery. Your healthcare provider may stop your JARDIANCE before you have surgery. Talk to your healthcare provider if you are having surgery about when to stop taking JARDIANCE and when to start it again. • are eating less, or there is a change in your diet. • are dehydrated. • have or have had problems with your pancreas, including pancreatitis or surgery on your pancreas. • drink alcohol very often or drink a lot of alcohol in the short term ("binge" drinking). • have ever had an allergic reaction to JARDIANCE. • are pregnant or plan to become pregnant. JARDIANCE may harm your unborn baby. If you become pregnant while taking JARDIANCE, tell your healthcare provider as soon as possible. Talk with your healthcare provider about the best way to control your blood sugar while you are pregnant. • are breastfeeding or plan to breastfeed. JARDIANCE may pass into your breast milk and may harm your baby. Talk with your healthcare provider about the best way to feed your baby if you are taking JARDIANCE. Do not breastfeed while taking JARDIANCE. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. JARDIANCE may affect the way other medicines work, and other medicines may affect how JARDIANCE works. Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine. How should I take JARDIANCE? • Take JARDIANCE exactly as your healthcare provider tells you to take it. • Take JARDIANCE by mouth 1 time in the morning each day, with or without food. • Your healthcare provider will tell you how much JARDIANCE to take and when to take it. Your healthcare provider may change your dose if needed. • Your healthcare provider may tell you to take JARDIANCE along with other diabetes medicines. Low blood sugar can happen more often when JARDIANCE is taken with certain other diabetes medicines.

vider will tell you how much JARDIANCE to take and when to take it. Your healthcare provider may change your dose if needed. • Your healthcare provider may tell you to take JARDIANCE along with other diabetes medicines. Low blood sugar can happen more often when JARDIANCE is taken with certain other diabetes medicines. See " What are the possible side effects of JARDIANCE? " • If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take two doses of JARDIANCE at the same time. Talk with your healthcare provider if you have questions about a missed dose. • If you take too much JARDIANCE, call your healthcare provider or Poison Help line at 1-800-222-1222, or go to the nearest hospital emergency room right away. • When taking JARDIANCE, you may have sugar in your urine, which will show up on a urine test. • When your body is under some types of stress, such as fever, trauma (such as a car accident), infection, or surgery, the amount of diabetes medicine you need may change. Tell your healthcare provider right away if you have any of these conditions and follow your healthcare provider's instructions. • Your healthcare provider may do certain blood tests before you start JARDIANCE and during treatment as needed. What are the possible side effects of JARDIANCE? JARDIANCE may cause serious side effects, including: • See " What is the most important information I should know about JARDIANCE? " • Genital and urinary tract infections. JARDIANCE can cause serious infections in your genital area or urinary tract that could require hospitalization. A rare but serious bacterial infection called necrotizing fasciitis can cause damage to the tissue under the skin in the area between and around the anus and genitals (perineum). This infection may require hospitalization, multiple surgeries, and could lead to death. Seek medical attention immediately if you have a fever or you are feeling very weak, tired or uncomfortable (malaise), and you develop any of the following symptoms in the area between and around your anus and genitals: o pain or tenderness o swelling o redness of skin (erythema) Also tell your healthcare provider if you have any of these signs or symptoms of urinary tract infections or yeast infections: o Urinary tract infection: You may also have a fever, back pain, nausea, or vomiting. ▪ burning feeling when you urinate ▪ need to urinate often or right away ▪ pain in the lower part of your stomach (pelvis) ▪ blood in your urine o Vaginal yeast infection : ▪ vaginal odor ▪ white or yellowish vaginal discharge (may be lumpy or look like cottage cheese) ▪ vaginal itching o Yeast infection of the skin around the penis (balanitis or balanoposthitis): If you are uncircumcised, swelling may make it difficult to pull back the skin around the tip of your penis. Other symptoms include: ▪ redness, itching, or swelling of the penis ▪ bad smelling discharge from the penis ▪ rash on the penis ▪ pain in the skin around the penis Talk to your healthcare provider about what to do if you get symptoms of a yeast infection. They may suggest you use an over-the-counter antifungal medicine. Contact your healthcare provider right away if your symptoms do not improve after using an over-the-counter antifungal medicine. • Low blood sugar (hypoglycemia). In adults, if you take JARDIANCE with another medicine that can cause low blood sugar, such as a sulfonylurea or insulin, your risk of getting low blood sugar is higher. In children 10 years of age and older, the risk for low blood sugar is higher with JARDIANCE even if you do not use another medicine that can also lower blood sugar.

ou take JARDIANCE with another medicine that can cause low blood sugar, such as a sulfonylurea or insulin, your risk of getting low blood sugar is higher. In children 10 years of age and older, the risk for low blood sugar is higher with JARDIANCE even if you do not use another medicine that can also lower blood sugar. The dose of your sulfonylurea medicine or insulin may need to be lowered while you take JARDIANCE. Signs and symptoms of low blood sugar may include: o headache o drowsiness o weakness o irritability o hunger o fast heartbeat o confusion o shaking or feeling jittery o dizziness o sweating • Amputations. SGLT2 inhibitors may increase your risk of lower limb amputations. You may be at a higher risk of lower limb amputation if you: o have a history of amputation o have had blocked or narrowed blood vessels, usually in your leg o have had diabetic foot infection, ulcers or sores Call your healthcare provider right away if you have new pain or tenderness, any sores, ulcers, or infections in your leg or foot. Talk to your healthcare provider about proper foot care. • Serious allergic reactions. If you have any symptoms of a serious allergic reaction, stop taking JARDIANCE and call your healthcare provider right away or go to the nearest hospital emergency room. See " Who should not take JARDIANCE? " . The most common side effects of JARDIANCE include: • urinary tract infections • yeast infections in females These are not all the possible side effects of JARDIANCE. For more information, ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. How should I store JARDIANCE? • Store JARDIANCE at room temperature between 68°F to 77°F (20°C to 25°C). • Keep JARDIANCE and all medicines out of the reach of children. General information about the safe and effective use of JARDIANCE. Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use JARDIANCE for a condition for which it is not prescribed. Do not give JARDIANCE to other people, even if they have the same symptoms you have. It may harm them. You can ask your pharmacist or healthcare provider for information about JARDIANCE that is written for health professionals. What are the ingredients in JARDIANCE? Active Ingredient: empagliflozin Inactive Ingredients: colloidal silicon dioxide, croscarmellose sodium, hydroxypropyl cellulose, lactose monohydrate, magnesium stearate, and microcrystalline cellulose. In addition, the film coating contains the following inactive ingredients: ferric oxide yellow, hypromellose, polyethylene glycol, talc, and titanium dioxide. Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA Licensed from: Boehringer Ingelheim International GmbH, Ingelheim, Germany JARDIANCE is a registered trademark of and used under license from Boehringer Ingelheim International GmbH. Boehringer Ingelheim Pharmaceuticals, Inc. either owns or uses the EMPA-REG OUTCOME ® , EMPEROR-Reduced ® , EMPEROR-Preserved ® , and EMPA-KIDNEY ® trademarks under license. The other brands listed are trademarks of their respective owners and are not trademarks of Boehringer Ingelheim Pharmaceuticals, Inc. Copyright © 2026 Boehringer Ingelheim International GmbH ALL RIGHTS RESERVED Distributed By: Cardinal Health Dublin, OH 43017 ER7381I Rev. C ER7383 Rev. B COL8914QA062026 For more information about JARDIANCE, including current prescribing information and Medication Guide, go to www.jardiance.com , scan the code, or call Boehringer Ingelheim Pharmaceuticals, Inc. at 1-800-542-6257. This Medication Guide has been approved by the U.S. Food and Drug Administration. Revised: January 2026 QR code

<table width="100%"><col width="2%"/><col width="24%"/><col width="23%"/><col width="25%"/><col width="25%"/><tbody><tr><td align="center" colspan="5" styleCode="Rrule Botrule Lrule Toprule " valign="top"><paragraph><content styleCode="bold">MEDICATION GUIDE </content> <content styleCode="bold">JARDIANCE^&#xAE; (jar DEE ans) </content> <content styleCode="bold">(empagliflozin tablets)</content> <content styleCode="bold">for oral use</content></paragraph></td></tr><tr><td colspan="5" styleCode="Rrule Lrule " valign="top"><paragraph><content styleCode="bold">What is the most important information I should know about JARDIANCE?</content> JARDIANCE can cause serious side effects, including:</paragraph><list listType="unordered"><item><caption>&#x2022;</caption><content styleCode="bold">Diabetic ketoacidosis (increased ketones in your blood or urine) in people with type 1 and other ketoacidosis.</content> JARDIANCE can cause ketoacidosis that can be life-threatening and may lead to death. Ketoacidosis is a serious condition which needs to be treated in a hospital. People with type 1 diabetes have a high risk of getting ketoacidosis. People with type 2 diabetes or pancreas problems also have an increased risk of getting ketoacidosis. Ketoacidosis can also happen in people who: are sick, cannot eat or drink as usual, skip meals, are on a diet high in fat and low in carbohydrates (ketogenic diet), take less than the usual amount of insulin or miss insulin doses, drink too much alcohol, have a loss of too much fluid from the body (volume depletion), or who have surgery. Ketoacidosis can happen even if your blood sugar is less than 250 mg/dL. Your healthcare provider may ask you to periodically check ketones in your urine or blood. <content styleCode="bold">Stop taking JARDIANCE and call your healthcare provider or get medical help right away if you get any of the following. If possible, check for ketones in your urine or blood, even if your blood sugar is less than 250 mg/dL:</content></item></list></td></tr><tr><td styleCode="Lrule " valign="top"/><td colspan="2" valign="top"><list listType="unordered"><item><caption>o</caption>nausea</item><item><caption>o</caption>vomiting</item><item><caption>o</caption>stomach-area (abdominal) pain</item></list></td><td valign="top"><list listType="unordered"><item><caption>o</caption>tiredness</item><item><caption>o</caption>trouble breathing</item><item><caption>o</caption>ketones in your urine or blood</item></list></td><td styleCode="Rrule " valign="top"/></tr><tr><td colspan="5" styleCode="Rrule Lrule Botrule " valign="top"><list listType="unordered"><item><caption>&#x2022;</caption><content styleCode="bold">Dehydration. JARDIANCE can cause some people to become dehydrated (the loss of body water and salt). Dehydration may cause you to feel dizzy, faint, light-headed, or weak, especially when you stand up (orthostatic hypotension).

="top"><list listType="unordered"><item><caption>&#x2022;</caption><content styleCode="bold">Dehydration. JARDIANCE can cause some people to become dehydrated (the loss of body water and salt). Dehydration may cause you to feel dizzy, faint, light-headed, or weak, especially when you stand up (orthostatic hypotension). There have been reports of sudden worsening of kidney function in people who are taking JARDIANCE.</content> You may be at higher risk of dehydration if you:<list listType="unordered"><item><caption>o</caption>take medicines to lower your blood pressure, including diuretics (water pills)</item><item><caption>o</caption>are on low sodium (salt) diet</item><item><caption>o</caption>have kidney problems</item><item><caption>o</caption>are 65 years of age or older<paragraph>Talk to your healthcare provider about what you can do to prevent dehydration including how much fluid you should drink on a daily basis. Call your healthcare provider right away if you reduce the amount of food or liquid you drink, for example if you are sick or you cannot eat, or start to lose liquids from your body, for example from vomiting, diarrhea or being in the sun too long.</paragraph></item></list></item></list></td></tr><tr><td colspan="5" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">What is JARDIANCE?</content> JARDIANCE is a prescription medicine used to:</paragraph><list listType="unordered"><item><caption>o</caption>reduce the risk of cardiovascular death and hospitalization for heart failure in adults with heart failure, when the heart cannot pump enough blood to the rest of your body.</item><item><caption>o</caption>reduce the risk of further worsening of kidney disease, end-stage kidney disease (ESKD), death due to cardiovascular disease, and hospitalization in adults with chronic kidney disease.</item><item><caption>o</caption>reduce the risk of cardiovascular death in adults with type 2 diabetes and who also have known cardiovascular disease.</item><item><caption>o</caption>lower blood sugar (glucose) along with diet and exercise in adults and children who are 10 years of age and older with type 2 diabetes.</item></list><paragraph>JARDIANCE is not for use to lower blood sugar (glucose) in people with type 1 diabetes. It may increase their risk of diabetic ketoacidosis (increased ketones in blood or urine). JARDIANCE is not for use to lower blood sugar (glucose) in people with type 2 diabetes who have severe kidney problems, because it may not work. JARDIANCE is not for people with polycystic kidney disease, or who are taking or have recently received certain types of immunosuppressive therapy to treat kidney disease. JARDIANCE is not expected to work if you have these conditions. It is not known if JARDIANCE is safe and effective in children under 10 years of age.</paragraph></td></tr><tr><td colspan="5" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">Who should not take JARDIANCE? </content> <content styleCode="bold">Do not take JARDIANCE if you:</content></paragraph><list listType="unordered"><item><caption>&#x2022;</caption>are allergic to empagliflozin or any of the ingredients in JARDIANCE. See the end of this Medication Guide for a complete list of ingredients in JARDIANCE.

take JARDIANCE? </content> <content styleCode="bold">Do not take JARDIANCE if you:</content></paragraph><list listType="unordered"><item><caption>&#x2022;</caption>are allergic to empagliflozin or any of the ingredients in JARDIANCE. See the end of this Medication Guide for a complete list of ingredients in JARDIANCE. Symptoms of a serious allergic reaction to JARDIANCE may include:<list listType="unordered"><item><caption>o</caption>rash</item><item><caption>o</caption>raised, red areas on your skin (hives)</item><item><caption>o</caption>swelling of your face, lips, mouth, and throat that may cause difficulty in breathing or swallowing<paragraph>If you have any of these symptoms, stop taking JARDIANCE and call your healthcare provider right away or go to the nearest hospital emergency room.</paragraph></item></list></item></list></td></tr><tr><td colspan="5" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">What should I tell my healthcare provider before taking JARDIANCE? </content> <content styleCode="bold">Before taking JARDIANCE, tell your healthcare provider about all of your medical conditions, including if you:</content></paragraph><list listType="unordered"><item><caption>&#x2022;</caption>have type 1 diabetes or have had diabetic ketoacidosis.</item><item><caption>&#x2022;</caption>have a decrease in your insulin dose.</item><item><caption>&#x2022;</caption>have a serious infection.</item><item><caption>&#x2022;</caption>have a history of infection of the vagina or penis.</item><item><caption>&#x2022;</caption>have a history of amputation.</item><item><caption>&#x2022;</caption>have kidney problems.</item><item><caption>&#x2022;</caption>have liver problems.</item><item><caption>&#x2022;</caption>have a history of urinary tract infections or problems with urination.</item><item><caption>&#x2022;</caption>are on a low sodium (salt) diet. Your healthcare provider may change your diet or your dose.</item><item><caption>&#x2022;</caption>are going to have surgery. Your healthcare provider may stop your JARDIANCE before you have surgery. Talk to your healthcare provider if you are having surgery about when to stop taking JARDIANCE and when to start it again.</item><item><caption>&#x2022;</caption>are eating less, or there is a change in your diet.</item><item><caption>&#x2022;</caption>are dehydrated.</item><item><caption>&#x2022;</caption>have or have had problems with your pancreas, including pancreatitis or surgery on your pancreas.</item><item><caption>&#x2022;</caption>drink alcohol very often or drink a lot of alcohol in the short term (&quot;binge&quot; drinking).</item><item><caption>&#x2022;</caption>have ever had an allergic reaction to JARDIANCE.</item><item><caption>&#x2022;</caption>are pregnant or plan to become pregnant. JARDIANCE may harm your unborn baby. If you become pregnant while taking JARDIANCE, tell your healthcare provider as soon as possible. Talk with your healthcare provider about the best way to control your blood sugar while you are pregnant.</item><item><caption>&#x2022;</caption>are breastfeeding or plan to breastfeed. JARDIANCE may pass into your breast milk and may harm your baby. Talk with your healthcare provider about the best way to feed your baby if you are taking JARDIANCE. Do not breastfeed while taking JARDIANCE.</item></list><paragraph><content styleCode="bold">Tell your healthcare provider about all the medicines you take,</content> including prescription and over-the-counter medicines, vitamins, and herbal supplements. JARDIANCE may affect the way other medicines work, and other medicines may affect how JARDIANCE works. Know the medicines you take.

<content styleCode="bold">Tell your healthcare provider about all the medicines you take,</content> including prescription and over-the-counter medicines, vitamins, and herbal supplements. JARDIANCE may affect the way other medicines work, and other medicines may affect how JARDIANCE works. Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine.</paragraph></td></tr><tr><td colspan="5" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">How should I take JARDIANCE?</content></paragraph><list listType="unordered"><item><caption>&#x2022;</caption>Take JARDIANCE exactly as your healthcare provider tells you to take it.</item><item><caption>&#x2022;</caption>Take JARDIANCE by mouth 1 time in the morning each day, with or without food.</item><item><caption>&#x2022;</caption>Your healthcare provider will tell you how much JARDIANCE to take and when to take it. Your healthcare provider may change your dose if needed.</item><item><caption>&#x2022;</caption>Your healthcare provider may tell you to take JARDIANCE along with other diabetes medicines. Low blood sugar can happen more often when JARDIANCE is taken with certain other diabetes medicines. See <content styleCode="bold">&quot;<linkHtml href="#_Refwhatare">What are the possible side effects of JARDIANCE?</linkHtml>&quot;</content></item><item><caption>&#x2022;</caption>If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take two doses of JARDIANCE at the same time. Talk with your healthcare provider if you have questions about a missed dose.</item><item><caption>&#x2022;</caption>If you take too much JARDIANCE, call your healthcare provider or Poison Help line at 1-800-222-1222, or go to the nearest hospital emergency room right away.</item><item><caption>&#x2022;</caption>When taking JARDIANCE, you may have sugar in your urine, which will show up on a urine test.</item><item><caption>&#x2022;</caption>When your body is under some types of stress, such as fever, trauma (such as a car accident), infection, or surgery, the amount of diabetes medicine you need may change. Tell your healthcare provider right away if you have any of these conditions and follow your healthcare provider&apos;s instructions.</item><item><caption>&#x2022;</caption>Your healthcare provider may do certain blood tests before you start JARDIANCE and during treatment as needed.</item></list></td></tr><tr><td colspan="5" styleCode="Rrule Lrule " valign="top"><paragraph><content styleCode="bold">What are the possible side effects of JARDIANCE?</content> <content styleCode="bold">JARDIANCE may cause serious side effects, including:</content></paragraph><list listType="unordered"><item><caption>&#x2022;</caption>See <content styleCode="bold">&quot;<linkHtml href="#_Refwhatis">What is the most important information I should know about JARDIANCE?</linkHtml>&quot;</content></item><item><caption>&#x2022;</caption><content styleCode="bold">Genital and urinary tract infections.</content> JARDIANCE can cause serious infections in your genital area or urinary tract that could require hospitalization. <content styleCode="bold">A rare but serious bacterial infection called necrotizing fasciitis can cause damage to the tissue under the skin in the area between and around the anus and genitals (perineum).</content> This infection may require hospitalization, multiple surgeries, and could lead to death.

hospitalization. <content styleCode="bold">A rare but serious bacterial infection called necrotizing fasciitis can cause damage to the tissue under the skin in the area between and around the anus and genitals (perineum).</content> This infection may require hospitalization, multiple surgeries, and could lead to death. <content styleCode="bold">Seek medical attention immediately if you have a fever or you are feeling very weak, tired or uncomfortable (malaise), and you develop any of the following symptoms in the area between and around your anus and genitals:</content></item></list></td></tr><tr><td styleCode="Lrule " valign="top"/><td valign="top"><list listType="unordered"><item><caption>o</caption>pain or tenderness</item></list></td><td valign="top"><list listType="unordered"><item><caption>o</caption>swelling</item></list></td><td colspan="2" styleCode="Rrule " valign="top"><list listType="unordered"><item><caption>o</caption>redness of skin (erythema)</item></list></td></tr><tr><td styleCode="Lrule " valign="top"/><td colspan="4" styleCode="Rrule " valign="top"><paragraph>Also tell your healthcare provider if you have any of these signs or symptoms of urinary tract infections or yeast infections:</paragraph></td></tr><tr><td styleCode="Lrule " valign="top"/><td colspan="4" styleCode="Rrule " valign="top"><list listType="unordered"><item><caption>o</caption><content styleCode="bold">Urinary tract infection:</content>You may also have a fever, back pain, nausea, or vomiting.<list listType="unordered"><item><caption>&#x25AA;</caption>burning feeling when you urinate</item><item><caption>&#x25AA;</caption>need to urinate often or right away</item><item><caption>&#x25AA;</caption>pain in the lower part of your stomach (pelvis)</item><item><caption>&#x25AA;</caption>blood in your urine</item></list></item><item><caption>o</caption><content styleCode="bold">Vaginal yeast infection</content>:<list listType="unordered"><item><caption>&#x25AA;</caption>vaginal odor</item><item><caption>&#x25AA;</caption>white or yellowish vaginal discharge (may be lumpy or look like cottage cheese)</item><item><caption>&#x25AA;</caption>vaginal itching</item></list></item><item><caption>o</caption><content styleCode="bold">Yeast infection of the skin around the penis (balanitis or balanoposthitis):</content> If you are uncircumcised, swelling may make it difficult to pull back the skin around the tip of your penis. Other symptoms include:</item></list></td></tr><tr><td styleCode="Lrule " valign="top"/><td valign="top"/><td valign="top"><list listType="unordered"><item><caption>&#x25AA;</caption>redness, itching, or swelling of the penis</item><item><caption>&#x25AA;</caption>bad smelling discharge from the penis</item></list></td><td colspan="2" styleCode="Rrule " valign="top"><list listType="unordered"><item><caption>&#x25AA;</caption>rash on the penis</item><item><caption>&#x25AA;</caption>pain in the skin around the penis</item></list></td></tr><tr><td styleCode="Lrule " valign="top"/><td valign="top"/><td colspan="3" styleCode="Rrule " valign="top"><paragraph>Talk to your healthcare provider about what to do if you get symptoms of a yeast infection. They may suggest you use an over-the-counter antifungal medicine. Contact your healthcare provider right away if your symptoms do not improve after using an over-the-counter antifungal medicine.</paragraph></td></tr><tr><td colspan="5" styleCode="Rrule Lrule " valign="top"><list listType="unordered"><item><caption>&#x2022;</caption><content styleCode="bold">Low blood sugar (hypoglycemia).</content> In adults, if you take JARDIANCE with another medicine that can cause low blood sugar, such as a sulfonylurea or insulin, your risk of getting low blood sugar is higher.

e Lrule " valign="top"><list listType="unordered"><item><caption>&#x2022;</caption><content styleCode="bold">Low blood sugar (hypoglycemia).</content> In adults, if you take JARDIANCE with another medicine that can cause low blood sugar, such as a sulfonylurea or insulin, your risk of getting low blood sugar is higher. In children 10 years of age and older, the risk for low blood sugar is higher with JARDIANCE even if you do not use another medicine that can also lower blood sugar. The dose of your sulfonylurea medicine or insulin may need to be lowered while you take JARDIANCE. Signs and symptoms of low blood sugar may include:</item></list></td></tr><tr><td styleCode="Lrule " valign="top"/><td valign="top"><list listType="unordered"><item><caption>o</caption>headache</item><item><caption>o</caption>drowsiness</item><item><caption>o</caption>weakness</item></list></td><td valign="top"><list listType="unordered"><item><caption>o</caption>irritability</item><item><caption>o</caption>hunger</item><item><caption>o</caption>fast heartbeat</item></list></td><td valign="top"><list listType="unordered"><item><caption>o</caption>confusion</item><item><caption>o</caption>shaking or feeling jittery</item></list></td><td styleCode="Rrule " valign="top"><list listType="unordered"><item><caption>o</caption>dizziness</item><item><caption>o</caption>sweating</item></list></td></tr><tr><td colspan="5" styleCode="Rrule Lrule Botrule " valign="top"><list listType="unordered"><item><caption>&#x2022;</caption><content styleCode="bold">Amputations. SGLT2 inhibitors may increase your risk of lower limb amputations.</content> You may be at a higher risk of lower limb amputation if you:<list listType="unordered"><item><caption>o</caption>have a history of amputation</item><item><caption>o</caption>have had blocked or narrowed blood vessels, usually in your leg</item><item><caption>o</caption>have had diabetic foot infection, ulcers or sores<paragraph><content styleCode="bold">Call your healthcare provider right away if you have new pain or tenderness, any sores, ulcers, or infections in your leg or foot.</content> Talk to your healthcare provider about proper foot care.</paragraph></item></list></item><item><caption>&#x2022;</caption><content styleCode="bold">Serious allergic reactions.</content> If you have any symptoms of a serious allergic reaction, stop taking JARDIANCE and call your healthcare provider right away or go to the nearest hospital emergency room. See <content styleCode="bold">&quot;<linkHtml href="#_Refnot">Who should not take JARDIANCE?</linkHtml>&quot;</content>.</item></list><paragraph><content styleCode="bold">The most common side effects of JARDIANCE include:</content></paragraph><list listType="unordered"><item><caption>&#x2022;</caption>urinary tract infections</item><item><caption>&#x2022;</caption>yeast infections in females</item></list><paragraph>These are not all the possible side effects of JARDIANCE. For more information, ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects.

aption>&#x2022;</caption>urinary tract infections</item><item><caption>&#x2022;</caption>yeast infections in females</item></list><paragraph>These are not all the possible side effects of JARDIANCE. For more information, ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.</paragraph></td></tr><tr><td colspan="5" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">How should I store JARDIANCE?</content></paragraph><list listType="unordered"><item><caption>&#x2022;</caption>Store JARDIANCE at room temperature between 68&#xB0;F to 77&#xB0;F (20&#xB0;C to 25&#xB0;C).</item><item><caption>&#x2022;</caption><content styleCode="bold">Keep JARDIANCE and all medicines out of the reach of children.</content></item></list></td></tr><tr><td colspan="5" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">General information about the safe and effective use of JARDIANCE.</content> Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use JARDIANCE for a condition for which it is not prescribed. Do not give JARDIANCE to other people, even if they have the same symptoms you have. It may harm them. You can ask your pharmacist or healthcare provider for information about JARDIANCE that is written for health professionals.</paragraph></td></tr><tr><td colspan="5" styleCode="Rrule Lrule Botrule " valign="top"><paragraph><content styleCode="bold">What are the ingredients in JARDIANCE?</content> <content styleCode="bold">Active Ingredient:</content> empagliflozin <content styleCode="bold">Inactive Ingredients:</content> colloidal silicon dioxide, croscarmellose sodium, hydroxypropyl cellulose, lactose monohydrate, magnesium stearate, and microcrystalline cellulose. In addition, the film coating contains the following inactive ingredients: ferric oxide yellow, hypromellose, polyethylene glycol, talc, and titanium dioxide. Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA Licensed from: Boehringer Ingelheim International GmbH, Ingelheim, Germany JARDIANCE is a registered trademark of and used under license from Boehringer Ingelheim International GmbH. Boehringer Ingelheim Pharmaceuticals, Inc. either owns or uses the EMPA-REG OUTCOME^&#xAE;, EMPEROR-Reduced^&#xAE;, EMPEROR-Preserved^&#xAE;, and EMPA-KIDNEY^&#xAE; trademarks under license. The other brands listed are trademarks of their respective owners and are not trademarks of Boehringer Ingelheim Pharmaceuticals, Inc. Copyright &#xA9; 2026 Boehringer Ingelheim International GmbH ALL RIGHTS RESERVED </paragraph><paragraph><content styleCode="bold">Distributed By:</content></paragraph><paragraph><content styleCode="bold">Cardinal Health </content></paragraph><paragraph>Dublin, OH 43017</paragraph><paragraph>ER7381I Rev. C</paragraph><paragraph>ER7383 Rev. B</paragraph><paragraph>COL8914QA062026 For more information about JARDIANCE, including current prescribing information and Medication Guide, go to <content styleCode="bold">www.jardiance.com</content>, scan the code, or call Boehringer Ingelheim Pharmaceuticals, Inc. at 1-800-542-6257.</paragraph><renderMultiMedia ID="id3814" referencedObject="MM8i"/></td></tr><tr><td colspan="4" valign="top"><paragraph>This Medication Guide has been approved by the U.S. Food and Drug Administration.</paragraph></td><td valign="top"><paragraph>Revised: January 2026</paragraph></td></tr></tbody></table>

<table ID="t3819014386" border="0" width="100%"><col/><col/><tbody><tr><td>Contraindications ( <linkHtml href="#Section_4">4</linkHtml>) </td><td align="right">12/2017</td></tr><tr><td>Warnings and Precautions ( <linkHtml href="#Section_5">5</linkHtml>) </td><td align="right">12/2017</td></tr></tbody></table>

1 INDICATIONS AND USAGE JARDIANCE is indicated: as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus, to reduce the risk of cardiovascular death in adult patients with type 2 diabetes mellitus and established cardiovascular disease. Limitations of Use JARDIANCE is not recommended for patients with type 1 diabetes or for the treatment of diabetic ketoacidosis. JARDIANCE is a sodium-glucose co-transporter 2 (SGLT2) inhibitor indicated: as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus, to reduce the risk of cardiovascular death in adult patients with type 2 diabetes mellitus and established cardiovascular disease. ( 1 ) Limitations of Use: Not for the treatment of type 1 diabetes mellitus or diabetic ketoacidosis ( 1 )

2 DOSAGE AND ADMINISTRATION The recommended dose of JARDIANCE is 10 mg once daily, taken in the morning, with or without food ( 2.1 ) Dose may be increased to 25 mg once daily ( 2.1 ) Assess renal function before initiating JARDIANCE. Do not initiate JARDIANCE if eGFR is below 45 mL/min/1.73 m 2 ( 2.2 ) Discontinue JARDIANCE if eGFR falls persistently below 45 mL/min/1.73 m 2 ( 2.2 ) 2.1 Recommended Dosage The recommended dose of JARDIANCE is 10 mg once daily in the morning, taken with or without food. In patients tolerating JARDIANCE, the dose may be increased to 25 mg [see Clinical Studies ( 14 )] . In patients with volume depletion, correcting this condition prior to initiation of JARDIANCE is recommended [see Warnings and Precautions ( 5.1 ), Use in Specific Populations ( 8.5 ) and Patient Counseling Information ( 17 )]. 2.2 Patients with Renal Impairment Assessment of renal function is recommended prior to initiation of JARDIANCE and periodically thereafter. JARDIANCE should not be initiated in patients with an eGFR less than 45 mL/min/1.73 m 2 . No dose adjustment is needed in patients with an eGFR greater than or equal to 45 mL/min/1.73 m 2 . JARDIANCE should be discontinued if eGFR is persistently less than 45 mL/min/1.73 m 2 [see Warnings and Precautions ( 5.1 , 5.3 ) and Use in Specific Populations ( 8.6 )] .

3 DOSAGE FORMS AND STRENGTHS JARDIANCE tablets available as: 10 mg pale yellow, round, biconvex and bevel-edged, film-coated tablets debossed with “S 10” on one side and the Boehringer Ingelheim company symbol on the other side. 25 mg pale yellow, oval, biconvex, film-coated tablets debossed with “S 25” on one side and the Boehringer Ingelheim company symbol on the other side. Tablets: 10 mg, 25 mg ( 3 )

4 CONTRAINDICATIONS History of serious hypersensitivity reaction to empagliflozin or any of the excipients in JARDIANCE [see Warnings and Precautions ( 5.7 )] . Severe renal impairment, end-stage renal disease, or dialysis [see Use in Specific Populations ( 8.6 )] . History of serious hypersensitivity reaction to empagliflozin or any of the excipients in JARDIANCE ( 4 ) Severe renal impairment, end-stage renal disease, or dialysis ( 4 )

5 WARNINGS AND PRECAUTIONS Hypotension: Before initiating JARDIANCE assess and correct volume status in patients with renal impairment, the elderly, in patients with low systolic blood pressure, and in patients on diuretics. Monitor for signs and symptoms during therapy. ( 5.1 ) Ketoacidosis: Assess patients who present with signs and symptoms of metabolic acidosis for ketoacidosis, regardless of blood glucose level. If suspected, discontinue JARDIANCE, evaluate and treat promptly. Before initiating JARDIANCE, consider risk factors for ketoacidosis. Patients on JARDIANCE may require monitoring and temporary discontinuation of therapy in clinical situations known to predispose to ketoacidosis. ( 5.2 ) Acute kidney injury and impairment in renal function: Consider temporarily discontinuing in settings of reduced oral intake or fluid losses. If acute kidney injury occurs, discontinue and promptly treat. Monitor renal function during therapy. ( 5.3 ) Urosepsis and Pyelonephritis: Evaluate patients for signs and symptoms of urinary tract infections and treat promptly, if indicated ( 5.4 ) Hypoglycemia: Consider lowering the dose of insulin secretagogue or insulin to reduce the risk of hypoglycemia when initiating JARDIANCE ( 5.5 ) Genital mycotic infections: Monitor and treat as appropriate ( 5.6 ) Hypersensitivity reactions: Discontinue JARDIANCE, treat promptly, and monitor until signs and symptoms resolve ( 5.7 ) Increased LDL-C: Monitor and treat as appropriate ( 5.8 ) 5.1 Hypotension JARDIANCE causes intravascular volume contraction. Symptomatic hypotension may occur after initiating JARDIANCE [see Adverse Reactions ( 6.1 )] particularly in patients with renal impairment, the elderly, in patients with low systolic blood pressure, and in patients on diuretics. Before initiating JARDIANCE, assess for volume contraction and correct volume status if indicated. Monitor for signs and symptoms of hypotension after initiating therapy and increase monitoring in clinical situations where volume contraction is expected [see Use in Specific Populations ( 8.5 )] . 5.2 Ketoacidosis Reports of ketoacidosis, a serious life-threatening condition requiring urgent hospitalization have been identified in postmarketing surveillance in patients with type 1 and type 2 diabetes mellitus receiving sodium glucose co-transporter-2 (SGLT2) inhibitors, including JARDIANCE. Fatal cases of ketoacidosis have been reported in patients taking JARDIANCE. JARDIANCE is not indicated for the treatment of patients with type 1 diabetes mellitus [see Indications and Usage ( 1 )] . Patients treated with JARDIANCE who present with signs and symptoms consistent with severe metabolic acidosis should be assessed for ketoacidosis regardless of presenting blood glucose levels, as ketoacidosis associated with JARDIANCE may be present even if blood glucose levels are less than 250 mg/dL. If ketoacidosis is suspected, JARDIANCE should be discontinued, patient should be evaluated, and prompt treatment should be instituted. Treatment of ketoacidosis may require insulin, fluid and carbohydrate replacement. In many of the postmarketing reports, and particularly in patients with type 1 diabetes, the presence of ketoacidosis was not immediately recognized and institution of treatment was delayed because presenting blood glucose levels were below those typically expected for diabetic ketoacidosis (often less than 250 mg/dL).

In many of the postmarketing reports, and particularly in patients with type 1 diabetes, the presence of ketoacidosis was not immediately recognized and institution of treatment was delayed because presenting blood glucose levels were below those typically expected for diabetic ketoacidosis (often less than 250 mg/dL). Signs and symptoms at presentation were consistent with dehydration and severe metabolic acidosis and included nausea, vomiting, abdominal pain, generalized malaise, and shortness of breath. In some but not all cases, factors predisposing to ketoacidosis such as insulin dose reduction, acute febrile illness, reduced caloric intake due to illness or surgery, pancreatic disorders suggesting insulin deficiency (e.g., type 1 diabetes, history of pancreatitis or pancreatic surgery), and alcohol abuse were identified. Before initiating JARDIANCE, consider factors in the patient history that may predispose to ketoacidosis including pancreatic insulin deficiency from any cause, caloric restriction, and alcohol abuse. In patients treated with JARDIANCE consider monitoring for ketoacidosis and temporarily discontinuing JARDIANCE in clinical situations known to predispose to ketoacidosis (e.g., prolonged fasting due to acute illness or surgery). 5.3 Acute Kidney Injury and Impairment in Renal Function JARDIANCE causes intravascular volume contraction [see Warnings and Precautions ( 5.1 )] and can cause renal impairment [see Adverse Reactions ( 6.1 )] . There have been postmarketing reports of acute kidney injury, some requiring hospitalization and dialysis, in patients receiving SGLT2 inhibitors, including JARDIANCE; some reports involved patients younger than 65 years of age. Before initiating JARDIANCE, consider factors that may predispose patients to acute kidney injury including hypovolemia, chronic renal insufficiency, congestive heart failure and concomitant medications (diuretics, ACE inhibitors, ARBs, NSAIDs). Consider temporarily discontinuing JARDIANCE in any setting of reduced oral intake (such as acute illness or fasting) or fluid losses (such as gastrointestinal illness or excessive heat exposure); monitor patients for signs and symptoms of acute kidney injury. If acute kidney injury occurs, discontinue JARDIANCE promptly and institute treatment. JARDIANCE increases serum creatinine and decreases eGFR. Patients with hypovolemia may be more susceptible to these changes. Renal function abnormalities can occur after initiating JARDIANCE [see Adverse Reactions ( 6.1 )] . Renal function should be evaluated prior to initiation of JARDIANCE and monitored periodically thereafter. More frequent renal function monitoring is recommended in patients with an eGFR below 60 mL/min/1.73 m 2 . Use of JARDIANCE is not recommended when eGFR is persistently less than 45 mL/min/1.73 m 2 and is contraindicated in patients with an eGFR less than 30 mL/min/1.73 m 2 [see Dosage and Administration ( 2.2 ), Contraindications ( 4 ) and Use in Specific Populations ( 8.6 )] . 5.4 Urosepsis and Pyelonephritis There have been postmarketing reports of serious urinary tract infections including urosepsis and pyelonephritis requiring hospitalization in patients receiving SGLT2 inhibitors, including JARDIANCE. Treatment with SGLT2 inhibitors increases the risk for urinary tract infections. Evaluate patients for signs and symptoms of urinary tract infections and treat promptly, if indicated [see Adverse Reactions ( 6 )] . 5.5 Hypoglycemia with Concomitant Use with Insulin and Insulin Secretagogues Insulin and insulin secretagogues are known to cause hypoglycemia. The risk of hypoglycemia is increased when JARDIANCE is used in combination with insulin secretagogues (e.g., sulfonylurea) or insulin [see Adverse Reactions ( 6.1 )] .

6 )] . 5.5 Hypoglycemia with Concomitant Use with Insulin and Insulin Secretagogues Insulin and insulin secretagogues are known to cause hypoglycemia. The risk of hypoglycemia is increased when JARDIANCE is used in combination with insulin secretagogues (e.g., sulfonylurea) or insulin [see Adverse Reactions ( 6.1 )] . Therefore, a lower dose of the insulin secretagogue or insulin may be required to reduce the risk of hypoglycemia when used in combination with JARDIANCE. 5.6 Genital Mycotic Infections JARDIANCE increases the risk for genital mycotic infections [see Adverse Reactions ( 6.1 )] . Patients with a history of chronic or recurrent genital mycotic infections were more likely to develop genital mycotic infections. Monitor and treat as appropriate. 5.7 Hypersensitivity Reactions There have been postmarketing reports of serious hypersensitivity reactions, (e.g., angioedema) in patients treated with JARDIANCE. If a hypersensitivity reaction occurs, discontinue JARDIANCE; treat promptly per standard of care, and monitor until signs and symptoms resolve. JARDIANCE is contraindicated in patients with a previous serious hypersensitivity reaction to empagliflozin or any of the excipients in JARDIANCE [see Contraindications ( 4 )] . 5.8 Increased Low-Density Lipoprotein Cholesterol (LDL-C) Increases in LDL-C can occur with JARDIANCE [see Adverse Reactions ( 6.1 )] . Monitor and treat as appropriate.

6 ADVERSE REACTIONS The following important adverse reactions are described below and elsewhere in the labeling: Hypotension [see Warnings and Precautions ( 5.1 )] Ketoacidosis [see Warnings and Precautions ( 5.2 )] Acute Kidney Injury and Impairment in Renal Function [see Warnings and Precautions ( 5.3 )] Urosepsis and Pyelonephritis [see Warnings and Precautions ( 5.4 )] Hypoglycemia with Concomitant Use with Insulin and Insulin Secretagogues [see Warnings and Precautions ( 5.5 )] Genital Mycotic Infections [see Warnings and Precautions ( 5.6 )] Hypersensitivity Reactions [see Warnings and Precautions ( 5.7 )] Increased Low-Density Lipoprotein Cholesterol (LDL-C) [see Warnings and Precautions ( 5.8 )] The most common adverse reactions associated with JARDIANCE (5% or greater incidence) were urinary tract infections and female genital mycotic infections ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Boehringer Ingelheim Pharmaceuticals, Inc. at 1-800-542-6257 or 1-800-459-9906 TTY, or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. Pool of Placebo-Controlled Trials evaluating JARDIANCE 10 and 25 mg The data in Table 1 are derived from a pool of four 24-week placebo-controlled trials and 18-week data from a placebo-controlled trial with insulin. JARDIANCE was used as monotherapy in one trial and as add-on therapy in four trials [see Clinical Studies ( 14 )] . These data reflect exposure of 1976 patients to JARDIANCE with a mean exposure duration of approximately 23 weeks. Patients received placebo (N=995), JARDIANCE 10 mg (N=999), or JARDIANCE 25 mg (N=977) once daily. The mean age of the population was 56 years and 3% were older than 75 years of age. More than half (55%) of the population was male; 46% were White, 50% were Asian, and 3% were Black or African American. At baseline, 57% of the population had diabetes more than 5 years and had a mean hemoglobin A1c (HbA1c) of 8%. Established microvascular complications of diabetes at baseline included diabetic nephropathy (7%), retinopathy (8%), or neuropathy (16%). Baseline renal function was normal or mildly impaired in 91% of patients and moderately impaired in 9% of patients (mean eGFR 86.8 mL/min/1.73 m 2 ). Table 1 shows common adverse reactions (excluding hypoglycemia) associated with the use of JARDIANCE. The adverse reactions were not present at baseline, occurred more commonly on JARDIANCE than on placebo and occurred in greater than or equal to 2% of patients treated with JARDIANCE 10 mg or JARDIANCE 25 mg. Table 1 Adverse Reactions Reported in ≥2% of Patients Treated with JARDIANCE and Greater than Placebo in Pooled Placebo-Controlled Clinical Studies of JARDIANCE Monotherapy or Combination Therapy a Predefined adverse event grouping, including, but not limited to, urinary tract infection, asymptomatic bacteriuria, cystitis b Female genital mycotic infections include the following adverse reactions: vulvovaginal mycotic infection, vaginal infection, vulvitis, vulvovaginal candidiasis, genital infection, genital candidiasis, genital infection fungal, genitourinary tract infection, vulvovaginitis, cervicitis, urogenital infection fungal, vaginitis bacterial.

ycotic infections include the following adverse reactions: vulvovaginal mycotic infection, vaginal infection, vulvitis, vulvovaginal candidiasis, genital infection, genital candidiasis, genital infection fungal, genitourinary tract infection, vulvovaginitis, cervicitis, urogenital infection fungal, vaginitis bacterial. Percentages calculated with the number of female subjects in each group as denominator: placebo (N=481), JARDIANCE 10 mg (N=443), JARDIANCE 25 mg (N=420). c Predefined adverse event grouping, including, but not limited to, polyuria, pollakiuria, and nocturia d Male genital mycotic infections include the following adverse reactions: balanoposthitis, balanitis, genital infections fungal, genitourinary tract infection, balanitis candida, scrotal abscess, penile infection. Percentages calculated with the number of male subjects in each group as denominator: placebo (N=514), JARDIANCE 10 mg (N=556), JARDIANCE 25 mg (N=557). Number (%) of Patients Placebo N=995 JARDIANCE 10 mg N=999 JARDIANCE 25 mg N=977 Urinary tract infection a 7.6% 9.3% 7.6% Female genital mycotic infections b 1.5% 5.4% 6.4% Upper respiratory tract infection 3.8% 3.1% 4.0% Increased urination c 1.0% 3.4% 3.2% Dyslipidemia 3.4% 3.9% 2.9% Arthralgia 2.2% 2.4% 2.3% Male genital mycotic infections d 0.4% 3.1% 1.6% Nausea 1.4% 2.3% 1.1% Thirst (including polydipsia) was reported in 0%, 1.7%, and 1.5% for placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Volume Depletion JARDIANCE causes an osmotic diuresis, which may lead to intravascular volume contraction and adverse reactions related to volume depletion. In the pool of five placebo-controlled clinical trials, adverse reactions related to volume depletion (e.g., blood pressure (ambulatory) decreased, blood pressure systolic decreased, dehydration, hypotension, hypovolemia, orthostatic hypotension, and syncope) were reported by 0.3%, 0.5%, and 0.3% of patients treated with placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. JARDIANCE may increase the risk of hypotension in patients at risk for volume contraction [see Warnings and Precautions ( 5.1 ) and Use in Specific Populations ( 8.5 , 8.6 )]. Increased Urination In the pool of five placebo-controlled clinical trials, adverse reactions of increased urination (e.g., polyuria, pollakiuria, and nocturia) occurred more frequently on JARDIANCE than on placebo (see Table 1). Specifically, nocturia was reported by 0.4%, 0.3%, and 0.8% of patients treated with placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Acute Impairment in Renal Function Treatment with JARDIANCE was associated with increases in serum creatinine and decreases in eGFR (see Table 2). Patients with moderate renal impairment at baseline had larger mean changes [see Warnings and Precautions ( 5.3 ) and Use in Specific Populations ( 8.5, 8.6 )] . In a long-term cardiovascular outcome trial, the acute impairment in renal function was observed to reverse after treatment discontinuation suggesting acute hemodynamic changes play a role in the renal function changes observed with empagliflozin. Table 2 Changes from Baseline in Serum Creatinine and eGFR a in the Pool of Four 24-week Placebo-Controlled Studies and Renal Impairment Study a Observed cases on treatment. b Subset of patients from renal impairment study with eGFR 30 to less than 60 mL/min/1.73 m 2 c Approximately 3 weeks after end of treatment.

zin. Table 2 Changes from Baseline in Serum Creatinine and eGFR a in the Pool of Four 24-week Placebo-Controlled Studies and Renal Impairment Study a Observed cases on treatment. b Subset of patients from renal impairment study with eGFR 30 to less than 60 mL/min/1.73 m 2 c Approximately 3 weeks after end of treatment. Pool of 24-Week Placebo-Controlled Studies Placebo JARDIANCE 10 mg JARDIANCE 25 mg Baseline Mean N 825 830 822 Creatinine (mg/dL) 0.84 0.85 0.85 eGFR (mL/min/1.73 m 2 ) 87.3 87.1 87.8 Week 12 Change N 771 797 783 Creatinine (mg/dL) 0.00 0.02 0.01 eGFR (mL/min/1.73 m 2 ) -0.3 -1.3 -1.4 Week 24 Change N 708 769 754 Creatinine (mg/dL) 0.00 0.01 0.01 eGFR (mL/min/1.73 m 2 ) -0.3 -0.6 -1.4 Moderate Renal Impairment b Placebo JARDIANCE 25 mg Baseline Mean N 187 -- 187 Creatinine (mg/dL) 1.49 -- 1.46 eGFR (mL/min/1.73 m 2 ) 44.3 -- 45.4 Week 12 Change N 176 -- 179 Creatinine (mg/dL) 0.01 -- 0.12 eGFR (mL/min/1.73 m 2 ) 0.1 -- -3.8 Week 24 Change N 170 -- 171 Creatinine (mg/dL) 0.01 -- 0.10 eGFR (mL/min/1.73 m 2 ) 0.2 -- -3.2 Week 52 Change N 164 -- 162 Creatinine (mg/dL) 0.02 -- 0.11 eGFR (mL/min/1.73 m 2 ) -0.3 -- -2.8 Post-treatment Change c N 98 -- 103 Creatinine (mg/dL) 0.03 -- 0.02 eGFR (mL/min/1.73 m 2 ) 0.16 -- 1.48 Hypoglycemia The incidence of hypoglycemia by study is shown in Table 3. The incidence of hypoglycemia increased when JARDIANCE was administered with insulin or sulfonylurea [see Warnings and Precautions ( 5.5 )] . Table 3 Incidence of Overall a and Severe b Hypoglycemic Events in Placebo-Controlled Clinical Studies c a Overall hypoglycemic events: plasma or capillary glucose of less than or equal to 70 mg/dL b Severe hypoglycemic events: requiring assistance regardless of blood glucose c Treated set (patients who had received at least one dose of study drug) d Insulin dose could not be adjusted during the initial 18 week treatment period Monotherapy (24 weeks) Placebo (n=229) JARDIANCE 10 mg (n=224) JARDIANCE 25 mg (n=223) Overall (%) 0.4% 0.4% 0.4% Severe (%) 0% 0% 0% In Combination with Metformin (24 weeks) Placebo + Metformin (n=206) JARDIANCE 10 mg + Metformin (n=217) JARDIANCE 25 mg + Metformin (n=214) Overall (%) 0.5% 1.8% 1.4% Severe (%) 0% 0% 0% In Combination with Metformin + Sulfonylurea (24 weeks) Placebo (n=225) JARDIANCE 10 mg + Metformin + Sulfonylurea (n=224) JARDIANCE 25 mg + Metformin + Sulfonylurea (n=217) Overall (%) 8.4% 16.1% 11.5% Severe (%) 0% 0% 0% In Combination with Pioglitazone +/- Metformin (24 weeks) Placebo (n=165) JARDIANCE 10 mg + Pioglitazone +/- Metformin (n=165) JARDIANCE 25 mg + Pioglitazone +/- Metformin (n=168) Overall (%) 1.8% 1.2% 2.4% Severe (%) 0% 0% 0% In Combination with Basal Insulin +/- Metformin (18 weeks d ) Placebo (n=170) JARDIANCE 10 mg (n=169) JARDIANCE 25 mg (n=155) Overall (%) 20.6% 19.5% 28.4% Severe (%) 0% 0% 1.3% In Combination with MDI Insulin +/-Metformin (18 weeks d ) Placebo (n=188) JARDIANCE 10 mg (n=186) JARDIANCE 25 mg (n=189) Overall (%) 37.2% 39.8% 41.3% Severe (%) 0.5% 0.5% 0.5% Genital Mycotic Infections In the pool of five placebo-controlled clinical trials, the incidence of genital mycotic infections (e.g., vaginal mycotic infection, vaginal infection, genital infection fungal, vulvovaginal candidiasis, and vulvitis) was increased in patients treated with JARDIANCE compared to placebo, occurring in 0.9%, 4.1%, and 3.7% of patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Discontinuation from study due to genital infection occurred in 0% of placebo-treated patients and 0.2% of patients treated with either JARDIANCE 10 or 25 mg. Genital mycotic infections occurred more frequently in female than male patients (see Table 1).

d to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Discontinuation from study due to genital infection occurred in 0% of placebo-treated patients and 0.2% of patients treated with either JARDIANCE 10 or 25 mg. Genital mycotic infections occurred more frequently in female than male patients (see Table 1). Phimosis occurred more frequently in male patients treated with JARDIANCE 10 mg (less than 0.1%) and JARDIANCE 25 mg (0.1%) than placebo (0%). Urinary Tract Infections In the pool of five placebo-controlled clinical trials, the incidence of urinary tract infections (e.g., urinary tract infection, asymptomatic bacteriuria, and cystitis) was increased in patients treated with JARDIANCE compared to placebo (see Table 1). Patients with a history of chronic or recurrent urinary tract infections were more likely to experience a urinary tract infection. The rate of treatment discontinuation due to urinary tract infections was 0.1%, 0.2%, and 0.1% for placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. Urinary tract infections occurred more frequently in female patients. The incidence of urinary tract infections in female patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg was 16.6%, 18.4%, and 17.0%, respectively. The incidence of urinary tract infections in male patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg was 3.2%, 3.6%, and 4.1%, respectively [see Warnings and Precautions ( 5.4 ) and Use in Specific Populations ( 8.5 )] . Laboratory Tests Increase in Low-Density Lipoprotein Cholesterol (LDL-C) Dose-related increases in low-density lipoprotein cholesterol (LDL-C) were observed in patients treated with JARDIANCE. LDL-C increased by 2.3%, 4.6%, and 6.5% in patients treated with placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively [see Warnings and Precautions ( 5.8 )] . The range of mean baseline LDL-C levels was 90.3 to 90.6 mg/dL across treatment groups. Increase in Hematocrit In a pool of four placebo-controlled studies, median hematocrit decreased by 1.3% in placebo and increased by 2.8% in JARDIANCE 10 mg and 2.8% in JARDIANCE 25 mg treated patients. At the end of treatment, 0.6%, 2.7%, and 3.5% of patients with hematocrits initially within the reference range had values above the upper limit of the reference range with placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively. 6.2 Postmarketing Experience Additional adverse reactions have been identified during postapproval use of JARDIANCE. Because these reactions are reported voluntarily from a population of uncertain size, it is generally not possible to reliably estimate their frequency or establish a causal relationship to drug exposure. Ketoacidosis [see Warnings and Precautions ( 5.2 )] Urosepsis and pyelonephritis [see Warnings and Precautions ( 5.4 )] Angioedema [see Warnings and Precautions ( 5.7 )] Skin reactions (e.g., rash, urticaria)

<table ID="t30763528" border="0" frame="void" rules="none" width="100%"><caption>Table 1 Adverse Reactions Reported in &#x2265;2% of Patients Treated with JARDIANCE and Greater than Placebo in Pooled Placebo-Controlled Clinical Studies of JARDIANCE Monotherapy or Combination Therapy</caption><col width="34%"/><col width="22%"/><col width="22%"/><col width="22%"/><tfoot><tr><td colspan="4">^aPredefined adverse event grouping, including, but not limited to, urinary tract infection, asymptomatic bacteriuria, cystitis </td></tr><tr><td colspan="4">^bFemale genital mycotic infections include the following adverse reactions: vulvovaginal mycotic infection, vaginal infection, vulvitis, vulvovaginal candidiasis, genital infection, genital candidiasis, genital infection fungal, genitourinary tract infection, vulvovaginitis, cervicitis, urogenital infection fungal, vaginitis bacterial. Percentages calculated with the number of female subjects in each group as denominator: placebo (N=481), JARDIANCE 10 mg (N=443), JARDIANCE 25 mg (N=420). </td></tr><tr><td colspan="4">^cPredefined adverse event grouping, including, but not limited to, polyuria, pollakiuria, and nocturia </td></tr><tr><td colspan="4">^dMale genital mycotic infections include the following adverse reactions: balanoposthitis, balanitis, genital infections fungal, genitourinary tract infection, balanitis candida, scrotal abscess, penile infection. Percentages calculated with the number of male subjects in each group as denominator: placebo (N=514), JARDIANCE 10 mg (N=556), JARDIANCE 25 mg (N=557).

ollowing adverse reactions: balanoposthitis, balanitis, genital infections fungal, genitourinary tract infection, balanitis candida, scrotal abscess, penile infection. Percentages calculated with the number of male subjects in each group as denominator: placebo (N=514), JARDIANCE 10 mg (N=556), JARDIANCE 25 mg (N=557). </td></tr></tfoot><tbody><tr><td rowspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td colspan="3" align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Number (%) of Patients</content></td></tr><tr><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Placebo N=995 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 10 mg N=999 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg N=977 </content></td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Urinary tract infection ^a</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">7.6%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">9.3%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">7.6%</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Female genital mycotic infections ^b</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.5%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">5.4%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">6.4%</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Upper respiratory tract infection</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">3.8%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">3.1%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">4.0%</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Increased urination ^c</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">3.4%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">3.2%</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Dyslipidemia</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">3.4%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">3.9%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">2.9%</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Arthralgia</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">2.2%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">2.4%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">2.3%</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Male genital mycotic infections ^d</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.4%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">3.1%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.6%</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Nausea</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.4%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">2.3%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.1%</td></tr></tbody></table>

Lrule Rrule Toprule">1.6%</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Nausea</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.4%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">2.3%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.1%</td></tr></tbody></table> <table ID="t246251228" border="0" frame="below" rules="none" width="100%"><caption>Table 2 Changes from Baseline in Serum Creatinine and eGFR ^ain the Pool of Four 24-week Placebo-Controlled Studies and Renal Impairment Study </caption><col width="20%"/><col width="20%"/><col width="20%"/><col width="20%"/><col width="20%"/><tfoot><tr><td colspan="5">^aObserved cases on treatment. ^bSubset of patients from renal impairment study with eGFR 30 to less than 60 mL/min/1.73 m ² ^cApproximately 3 weeks after end of treatment.

="20%"/><col width="20%"/><col width="20%"/><col width="20%"/><col width="20%"/><tfoot><tr><td colspan="5">^aObserved cases on treatment. ^bSubset of patients from renal impairment study with eGFR 30 to less than 60 mL/min/1.73 m ² ^cApproximately 3 weeks after end of treatment. </td></tr></tfoot><tbody><tr><td colspan="2" rowspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td colspan="3" align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Pool of 24-Week Placebo-Controlled Studies</content></td></tr><tr><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Placebo</content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 10 mg</content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg</content></td></tr><tr><td rowspan="3" styleCode="Botrule Lrule Rrule Toprule">Baseline Mean</td><td styleCode="Botrule Lrule Rrule Toprule" valign="top">N</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">825</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">830</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">822</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">Creatinine (mg/dL)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.84</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.85</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.85</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">eGFR (mL/min/1.73 m ²) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">87.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">87.1</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">87.8</td></tr><tr><td rowspan="3" styleCode="Botrule Lrule Rrule Toprule">Week 12 Change</td><td styleCode="Botrule Lrule Rrule Toprule" valign="top">N</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">771</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">797</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">783</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">Creatinine (mg/dL)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.00</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.02</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.01</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">eGFR (mL/min/1.73 m ²) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-0.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-1.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-1.4</td></tr><tr><td rowspan="3" styleCode="Botrule Lrule Rrule Toprule">Week 24 Change</td><td styleCode="Botrule Lrule Rrule Toprule" valign="top">N</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">708</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">769</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">754</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">Creatinine (mg/dL)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.00</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.01</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.01</td></tr><tr><td styleCode="Botrule Lrule Rrule T

gn="top">Creatinine (mg/dL)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.00</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.01</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.01</td></tr><tr><td styleCode="Botrule Lrule Rrule T oprule" valign="top">eGFR (mL/min/1.73 m ²) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-0.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-0.6</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-1.4</td></tr><tr><td colspan="2" rowspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td colspan="3" align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Moderate Renal Impairment ^b</content></td></tr><tr><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Placebo</content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg</content></td></tr><tr><td rowspan="3" styleCode="Botrule Lrule Rrule Toprule">Baseline Mean</td><td styleCode="Botrule Lrule Rrule Toprule" valign="top">N</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">187</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">187</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">Creatinine (mg/dL)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">1.49</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">1.46</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">eGFR (mL/min/1.73 m ²) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">44.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">45.4</td></tr><tr><td rowspan="3" styleCode="Botrule Lrule Rrule Toprule">Week 12 Change</td><td styleCode="Botrule Lrule Rrule Toprule" valign="top">N</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">176</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">179</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">Creatinine (mg/dL)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.01</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.12</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">eGFR (mL/min/1.73 m ²) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.1</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-3.8</td></tr><tr><td rowspan="3" styleCode="Botrule Lrule Rrule Toprule">Week 24 Change</td><td styleCode="Botrule Lrule Rrule Toprule" valign="top">N</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">170</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">171</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">Creatinine (mg/dL)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"

><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">171</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">Creatinine (mg/dL)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top" >0.01</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.10</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">eGFR (mL/min/1.73 m ²) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.2</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-3.2</td></tr><tr><td rowspan="3" styleCode="Botrule Lrule Rrule Toprule">Week 52 Change</td><td styleCode="Botrule Lrule Rrule Toprule" valign="top">N</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">164</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">162</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">Creatinine (mg/dL)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.02</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.11</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">eGFR (mL/min/1.73 m ²) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-0.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-2.8</td></tr><tr><td rowspan="3" styleCode="Botrule Lrule Rrule Toprule">Post-treatment Change ^c</td><td styleCode="Botrule Lrule Rrule Toprule" valign="top">N</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">98</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">103</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">Creatinine (mg/dL)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.03</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.02</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">eGFR (mL/min/1.73 m ²) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.16</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">1.48</td></tr></tbody></table>

rule" valign="top">eGFR (mL/min/1.73 m ²) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.16</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">1.48</td></tr></tbody></table> <table ID="t34091128" border="0" frame="void" rules="none" width="100%"><caption>Table 3 Incidence of Overall ^aand Severe ^bHypoglycemic Events in Placebo-Controlled Clinical Studies ^c</caption><col width="31%"/><col width="23%"/><col width="23%"/><col width="23%"/><tfoot><tr><td colspan="4">^aOverall hypoglycemic events: plasma or capillary glucose of less than or equal to 70 mg/dL ^bSevere hypoglycemic events: requiring assistance regardless of blood glucose ^cTreated set (patients who had received at least one dose of study drug) ^dInsulin dose could not be adjusted during the initial 18 week treatment period </td></tr></tfoot><tbody><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Monotherapy (24 weeks) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Placebo (n=229) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 10 mg (n=224) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg (n=223) </content></td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule" valign="middle">Overall (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.4%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.4%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.4%</td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule" valign="middle">Severe (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">In Combination with Metformin (24 weeks) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Placebo + Metformin (n=206) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 10 mg + Metformin (n=217) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg + Metformin (n=214) </content></td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule" valign="middle">Overall (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.5%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.8%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.4%</td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule" valign="middle">Severe (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">In Combination with Metformin + Sulfonylurea (24 weeks) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Placebo (n=225) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 10 mg + Metformin + Sulfonylurea (n=224) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg + Metformin + Sulfony

tyleCode="bold">Placebo (n=225) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 10 mg + Metformin + Sulfonylurea (n=224) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg + Metformin + Sulfony lurea (n=217) </content></td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule" valign="middle">Overall (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">8.4%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">16.1%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">11.5%</td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule" valign="middle">Severe (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">In Combination with Pioglitazone +/- Metformin (24 weeks) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Placebo (n=165) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 10 mg + Pioglitazone +/- Metformin (n=165) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg + Pioglitazone +/- Metformin (n=168) </content></td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule" valign="middle">Overall (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.8%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.2%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">2.4%</td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule" valign="middle">Severe (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">In Combination with Basal Insulin</content><content styleCode="bold">+/- </content><content styleCode="bold">Metformin</content> <content styleCode="bold">(18 weeks ^d) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Placebo (n=170) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 10 mg (n=169) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg (n=155) </content></td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule" valign="middle">Overall (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">20.6%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">19.5%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">28.4%</td></tr><tr valign="top"><td styleCode="Botrule Lrule Rrule Toprule" valign="middle">Severe (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.3%</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">In Combination with MDI Insulin +/-Metformin (18 weeks ^d) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"><content styleCode="bold">Placebo (n=188) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"><content styleCode="bold">JARDIANCE 10 mg (n=186) </content></td><td ali

tformin (18 weeks ^d) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"><content styleCode="bold">Placebo (n=188) </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"><content styleCode="bold">JARDIANCE 10 mg (n=186) </content></td><td ali gn="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"><content styleCode="bold">JARDIANCE 25 mg (n=189) </content></td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Overall (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">37.2%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">39.8%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">41.3%</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Severe (%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.5%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.5%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">0.5%</td></tr></tbody></table>

7 DRUG INTERACTIONS 7.1 Diuretics Coadministration of empagliflozin with diuretics resulted in increased urine volume and frequency of voids, which might enhance the potential for volume depletion [see Warnings and Precautions ( 5.1 )] . 7.2 Insulin or Insulin Secretagogues Coadministration of empagliflozin with insulin or insulin secretagogues increases the risk for hypoglycemia [see Warnings and Precautions ( 5.5 )]. 7.3 Positive Urine Glucose Test Monitoring glycemic control with urine glucose tests is not recommended in patients taking SGLT2 inhibitors as SGLT2 inhibitors increase urinary glucose excretion and will lead to positive urine glucose tests. Use alternative methods to monitor glycemic control. 7.4 Interference with 1,5-anhydroglucitol (1,5-AG) Assay Monitoring glycemic control with 1,5-AG assay is not recommended as measurements of 1,5-AG are unreliable in assessing glycemic control in patients taking SGLT2 inhibitors. Use alternative methods to monitor glycemic control.

8 USE IN SPECIFIC POPULATIONS Pregnancy: Advise females of the potential risk to a fetus especially during the second and third trimesters ( 8.1 ) Lactation: JARDIANCE is not recommended when breastfeeding ( 8.2 ) Geriatric patients: Higher incidence of adverse reactions related to volume depletion and reduced renal function ( 5.1 , 5.3 , 8.5 ) Patients with renal impairment: Higher incidence of adverse reactions related to reduced renal function ( 2.2 , 5.3 , 8.6 ) 8.1 Pregnancy Risk Summary Based on animal data showing adverse renal effects, JARDIANCE is not recommended during the second and third trimesters of pregnancy. Limited data available with JARDIANCE in pregnant women are not sufficient to determine a drug-associated risk for major birth defects and miscarriage. There are risks to the mother and fetus associated with poorly controlled diabetes in pregnancy [see Clinical Considerations ] . In animal studies, adverse renal changes were observed in rats when empagliflozin was administered during a period of renal development corresponding to the late second and third trimesters of human pregnancy. Doses approximately 13-times the maximum clinical dose caused renal pelvic and tubule dilatations that were reversible. Empagliflozin was not teratogenic in rats and rabbits up to 300 mg/kg/day, which approximates 48-times and 128-times, respectively, the maximum clinical dose of 25 mg when administered during organogenesis [see Data ] . The estimated background risk of major birth defects is 6-10% in women with pre-gestational diabetes with a HbA1c >7 and has been reported to be as high as 20-25% in women with HbA1c >10. The estimated background risk of miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively. Clinical Considerations Disease-associated maternal and/or embryo/fetal risk: Poorly controlled diabetes in pregnancy increases the maternal risk for diabetic ketoacidosis, pre-eclampsia, spontaneous abortions, preterm delivery, stillbirth, and delivery complications. Poorly controlled diabetes increases the fetal risk for major birth defects, stillbirth, and macrosomia related morbidity. Data Animal Data Empagliflozin dosed directly to juvenile rats from postnatal day (PND) 21 until PND 90 at doses of 1, 10, 30 and 100 mg/kg/day caused increased kidney weights and renal tubular and pelvic dilatation at 100 mg/kg/day, which approximates 13-times the maximum clinical dose of 25 mg, based on AUC. These findings were not observed after a 13 week drug-free recovery period. These outcomes occurred with drug exposure during periods of renal development in rats that correspond to the late second and third trimester of human renal development. In embryo-fetal development studies in rats and rabbits, empagliflozin was administered for intervals coinciding with the first trimester period of organogenesis in humans. Doses up to 300 mg/kg/day, which approximates 48-times (rats) and 128-times (rabbits) the maximum clinical dose of 25 mg (based on AUC), did not result in adverse developmental effects. In rats, at higher doses of empagliflozin causing maternal toxicity, malformations of limb bones increased in fetuses at 700 mg/kg/day or 154-times the 25 mg maximum clinical dose. Empagliflozin crosses the placenta and reaches fetal tissues in rats.

5 mg (based on AUC), did not result in adverse developmental effects. In rats, at higher doses of empagliflozin causing maternal toxicity, malformations of limb bones increased in fetuses at 700 mg/kg/day or 154-times the 25 mg maximum clinical dose. Empagliflozin crosses the placenta and reaches fetal tissues in rats. In the rabbit, higher doses of empagliflozin resulted in maternal and fetal toxicity at 700 mg/kg/day, or 139-times the 25 mg maximum clinical dose. In pre- and postnatal development studies in pregnant rats, empagliflozin was administered from gestation day 6 through to lactation day 20 (weaning) at up to 100 mg/kg/day (approximately 16 times the 25 mg maximum clinical dose) without maternal toxicity. Reduced body weight was observed in the offspring at greater than or equal to 30 mg/kg/day (approximately 4 times the 25 mg maximum clinical dose). 8.2 Lactation Risk Summary There is no information regarding the presence of JARDIANCE in human milk, the effects of JARDIANCE on the breastfed infant or the effects on milk production. Empagliflozin is present in the milk of lactating rats [see Data ] . Since human kidney maturation occurs in utero and during the first 2 years of life when lactational exposure may occur, there may be risk to the developing human kidney. Because of the potential for serious adverse reactions in a breastfed infant, including the potential for empagliflozin to affect postnatal renal development, advise women that use of JARDIANCE is not recommended while breastfeeding. Data Empagliflozin was present at a low level in rat fetal tissues after a single oral dose to the dams at gestation day 18. In rat milk, the mean milk to plasma ratio ranged from 0.634 -5, and was greater than one from 2 to 24 hours post-dose. The mean maximal milk to plasma ratio of 5 occurred at 8 hours post-dose, suggesting accumulation of empagliflozin in the milk. Juvenile rats directly exposed to empagliflozin showed a risk to the developing kidney (renal pelvic and tubular dilatations) during maturation. 8.4 Pediatric Use The safety and effectiveness of JARDIANCE in pediatric patients under 18 years of age have not been established. 8.5 Geriatric Use No JARDIANCE dosage change is recommended based on age [see Dosage and Administration ( 2 )] . In studies assessing the efficacy of empagliflozin in improving glycemic control in patients with type 2 diabetes, a total of 2721 (32%) patients treated with empagliflozin were 65 years of age and older, and 491 (6%) were 75 years of age and older. JARDIANCE is expected to have diminished glycemic efficacy in elderly patients with renal impairment [see Use in Specific Populations ( 8.6 )] . The risk of volume depletion-related adverse reactions increased in patients who were 75 years of age and older to 2.1%, 2.3%, and 4.4% for placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg. The risk of urinary tract infections increased in patients who were 75 years of age and older to 10.5%, 15.7%, and 15.1% in patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively [see Warnings and Precautions ( 5.1 ) and Adverse Reactions ( 6.1 )] . 8.6 Renal Impairment The efficacy and safety of JARDIANCE were evaluated in a study of patients with mild and moderate renal impairment [see Clinical Studies ( 14.1 )] . In this study, 195 patients exposed to JARDIANCE had an eGFR between 60 and 90 mL/min/1.73 m 2 , 91 patients exposed to JARDIANCE had an eGFR between 45 and 60 mL/min/1.73 m 2 and 97 patients exposed to JARDIANCE had an eGFR between 30 and 45 mL/min/1.73 m 2 . The glucose lowering benefit of JARDIANCE 25 mg decreased in patients with worsening renal function.

RDIANCE had an eGFR between 60 and 90 mL/min/1.73 m 2 , 91 patients exposed to JARDIANCE had an eGFR between 45 and 60 mL/min/1.73 m 2 and 97 patients exposed to JARDIANCE had an eGFR between 30 and 45 mL/min/1.73 m 2 . The glucose lowering benefit of JARDIANCE 25 mg decreased in patients with worsening renal function. The risks of renal impairment [see Warnings and Precautions ( 5.3 )] , volume depletion adverse reactions and urinary tract infection-related adverse reactions increased with worsening renal function. In a large cardiovascular outcomes study, there were 1819 patients with eGFR below 60 mL/min/1.73 m 2 . The cardiovascular death findings in this subgroup were consistent with the overall findings [see Clinical Studies ( 14.2 )]. The efficacy and safety of JARDIANCE have not been established in patients with severe renal impairment, with ESRD, or receiving dialysis. JARDIANCE is not expected to be effective in these patient populations [see Dosage and Administration ( 2.2 ), Contraindications ( 4 ) and Warnings and Precautions ( 5.1, 5.3 )]. 8.7 Hepatic Impairment JARDIANCE may be used in patients with hepatic impairment [see Clinical Pharmacology ( 12.3 )] .

8.1 Pregnancy Risk Summary Based on animal data showing adverse renal effects, JARDIANCE is not recommended during the second and third trimesters of pregnancy. Limited data available with JARDIANCE in pregnant women are not sufficient to determine a drug-associated risk for major birth defects and miscarriage. There are risks to the mother and fetus associated with poorly controlled diabetes in pregnancy [see Clinical Considerations ] . In animal studies, adverse renal changes were observed in rats when empagliflozin was administered during a period of renal development corresponding to the late second and third trimesters of human pregnancy. Doses approximately 13-times the maximum clinical dose caused renal pelvic and tubule dilatations that were reversible. Empagliflozin was not teratogenic in rats and rabbits up to 300 mg/kg/day, which approximates 48-times and 128-times, respectively, the maximum clinical dose of 25 mg when administered during organogenesis [see Data ] . The estimated background risk of major birth defects is 6-10% in women with pre-gestational diabetes with a HbA1c >7 and has been reported to be as high as 20-25% in women with HbA1c >10. The estimated background risk of miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively. Clinical Considerations Disease-associated maternal and/or embryo/fetal risk: Poorly controlled diabetes in pregnancy increases the maternal risk for diabetic ketoacidosis, pre-eclampsia, spontaneous abortions, preterm delivery, stillbirth, and delivery complications. Poorly controlled diabetes increases the fetal risk for major birth defects, stillbirth, and macrosomia related morbidity. Data Animal Data Empagliflozin dosed directly to juvenile rats from postnatal day (PND) 21 until PND 90 at doses of 1, 10, 30 and 100 mg/kg/day caused increased kidney weights and renal tubular and pelvic dilatation at 100 mg/kg/day, which approximates 13-times the maximum clinical dose of 25 mg, based on AUC. These findings were not observed after a 13 week drug-free recovery period. These outcomes occurred with drug exposure during periods of renal development in rats that correspond to the late second and third trimester of human renal development. In embryo-fetal development studies in rats and rabbits, empagliflozin was administered for intervals coinciding with the first trimester period of organogenesis in humans. Doses up to 300 mg/kg/day, which approximates 48-times (rats) and 128-times (rabbits) the maximum clinical dose of 25 mg (based on AUC), did not result in adverse developmental effects. In rats, at higher doses of empagliflozin causing maternal toxicity, malformations of limb bones increased in fetuses at 700 mg/kg/day or 154-times the 25 mg maximum clinical dose. Empagliflozin crosses the placenta and reaches fetal tissues in rats. In the rabbit, higher doses of empagliflozin resulted in maternal and fetal toxicity at 700 mg/kg/day, or 139-times the 25 mg maximum clinical dose. In pre- and postnatal development studies in pregnant rats, empagliflozin was administered from gestation day 6 through to lactation day 20 (weaning) at up to 100 mg/kg/day (approximately 16 times the 25 mg maximum clinical dose) without maternal toxicity.

at 700 mg/kg/day, or 139-times the 25 mg maximum clinical dose. In pre- and postnatal development studies in pregnant rats, empagliflozin was administered from gestation day 6 through to lactation day 20 (weaning) at up to 100 mg/kg/day (approximately 16 times the 25 mg maximum clinical dose) without maternal toxicity. Reduced body weight was observed in the offspring at greater than or equal to 30 mg/kg/day (approximately 4 times the 25 mg maximum clinical dose).

8.5 Geriatric Use No JARDIANCE dosage change is recommended based on age [see Dosage and Administration ( 2 )] . In studies assessing the efficacy of empagliflozin in improving glycemic control in patients with type 2 diabetes, a total of 2721 (32%) patients treated with empagliflozin were 65 years of age and older, and 491 (6%) were 75 years of age and older. JARDIANCE is expected to have diminished glycemic efficacy in elderly patients with renal impairment [see Use in Specific Populations ( 8.6 )] . The risk of volume depletion-related adverse reactions increased in patients who were 75 years of age and older to 2.1%, 2.3%, and 4.4% for placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg. The risk of urinary tract infections increased in patients who were 75 years of age and older to 10.5%, 15.7%, and 15.1% in patients randomized to placebo, JARDIANCE 10 mg, and JARDIANCE 25 mg, respectively [see Warnings and Precautions ( 5.1 ) and Adverse Reactions ( 6.1 )] .

10 OVERDOSAGE In the event of an overdose with JARDIANCE, contact the Poison Control Center. Employ the usual supportive measures (e.g., remove unabsorbed material from the gastrointestinal tract, employ clinical monitoring, and institute supportive treatment) as dictated by the patient’s clinical status. Removal of empagliflozin by hemodialysis has not been studied.

11 DESCRIPTION JARDIANCE tablets contain empagliflozin, an orally-active inhibitor of the sodium-glucose co-transporter 2 (SGLT2). The chemical name of empagliflozin is D-Glucitol,1,5-anhydro-1-C-[4-chloro-3-[[4-[[(3S)-tetrahydro-3-furanyl]oxy]phenyl]methyl]phenyl]-, (1S). Its molecular formula is C 23 H 27 ClO 7 and the molecular weight is 450.91. The structural formula is: Empagliflozin is a white to yellowish, non-hygroscopic powder. It is very slightly soluble in water, sparingly soluble in methanol, slightly soluble in ethanol and acetonitrile; soluble in 50% acetonitrile/water; and practically insoluble in toluene. Each film-coated tablet of JARDIANCE contains 10 mg or 25 mg of empagliflozin (free base) and the following inactive ingredients: lactose monohydrate, microcrystalline cellulose, hydroxypropyl cellulose, croscarmellose sodium, colloidal silicon dioxide and magnesium stearate. In addition, the film coating contains the following inactive ingredients: hypromellose, titanium dioxide, talc, polyethylene glycol, and yellow ferric oxide. Empagliflozin structure

12 CLINICAL PHARMACOLOGY 12.1 Mechanism of Action Sodium-glucose co-transporter 2 (SGLT2) is the predominant transporter responsible for reabsorption of glucose from the glomerular filtrate back into the circulation. Empagliflozin is an inhibitor of SGLT2. By inhibiting SGLT2, empagliflozin reduces renal reabsorption of filtered glucose and lowers the renal threshold for glucose, and thereby increases urinary glucose excretion. 12.2 Pharmacodynamics Urinary Glucose Excretion In patients with type 2 diabetes, urinary glucose excretion increased immediately following a dose of JARDIANCE and was maintained at the end of a 4-week treatment period averaging at approximately 64 grams per day with 10 mg empagliflozin and 78 grams per day with 25 mg JARDIANCE once daily [see Clinical Studies ( 14 )]. Urinary Volume In a 5-day study, mean 24-hour urine volume increase from baseline was 341 mL on Day 1 and 135 mL on Day 5 of empagliflozin 25 mg once daily treatment. Cardiac Electrophysiology In a randomized, placebo-controlled, active-comparator, crossover study, 30 healthy subjects were administered a single oral dose of JARDIANCE 25 mg, JARDIANCE 200 mg (8 times the maximum dose), moxifloxacin, and placebo. No increase in QTc was observed with either 25 mg or 200 mg empagliflozin. 12.3 Pharmacokinetics Absorption The pharmacokinetics of empagliflozin has been characterized in healthy volunteers and patients with type 2 diabetes and no clinically relevant differences were noted between the two populations. After oral administration, peak plasma concentrations of empagliflozin were reached at 1.5 hours post-dose. Thereafter, plasma concentrations declined in a biphasic manner with a rapid distribution phase and a relatively slow terminal phase. The steady state mean plasma AUC and C max were 1870 nmol·h/L and 259 nmol/L, respectively, with 10 mg empagliflozin once daily treatment, and 4740 nmol·h/L and 687 nmol/L, respectively, with 25 mg empagliflozin once daily treatment. Systemic exposure of empagliflozin increased in a dose-proportional manner in the therapeutic dose range. The single-dose and steady-state pharmacokinetic parameters of empagliflozin were similar, suggesting linear pharmacokinetics with respect to time. Administration of 25 mg empagliflozin after intake of a high-fat and high-calorie meal resulted in slightly lower exposure; AUC decreased by approximately 16% and C max decreased by approximately 37%, compared to fasted condition. The observed effect of food on empagliflozin pharmacokinetics was not considered clinically relevant and empagliflozin may be administered with or without food. Distribution The apparent steady-state volume of distribution was estimated to be 73.8 L based on a population pharmacokinetic analysis. Following administration of an oral [ 14 C]-empagliflozin solution to healthy subjects, the red blood cell partitioning was approximately 36.8% and plasma protein binding was 86.2%. Metabolism No major metabolites of empagliflozin were detected in human plasma and the most abundant metabolites were three glucuronide conjugates (2-O-, 3-O-, and 6-O-glucuronide). Systemic exposure of each metabolite was less than 10% of total drug-related material. In vitro studies suggested that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT2B7, UGT1A3, UGT1A8, and UGT1A9.

(2-O-, 3-O-, and 6-O-glucuronide). Systemic exposure of each metabolite was less than 10% of total drug-related material. In vitro studies suggested that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT2B7, UGT1A3, UGT1A8, and UGT1A9. Elimination The apparent terminal elimination half-life of empagliflozin was estimated to be 12.4 h and apparent oral clearance was 10.6 L/h based on the population pharmacokinetic analysis. Following once-daily dosing, up to 22% accumulation, with respect to plasma AUC, was observed at steady-state, which was consistent with empagliflozin half-life. Following administration of an oral [ 14 C]-empagliflozin solution to healthy subjects, approximately 95.6% of the drug-related radioactivity was eliminated in feces (41.2%) or urine (54.4%). The majority of drug-related radioactivity recovered in feces was unchanged parent drug and approximately half of drug-related radioactivity excreted in urine was unchanged parent drug. Specific Populations Renal Impairment In patients with mild (eGFR: 60 to less than 90 mL/min/1.73 m 2 ), moderate (eGFR: 30 to less than 60 mL/min/1.73 m 2 ), and severe (eGFR: less than 30 mL/min/1.73 m 2 ) renal impairment and subjects with kidney failure/end stage renal disease (ESRD) patients, AUC of empagliflozin increased by approximately 18%, 20%, 66%, and 48%, respectively, compared to subjects with normal renal function. Peak plasma levels of empagliflozin were similar in subjects with moderate renal impairment and kidney failure/ESRD compared to patients with normal renal function. Peak plasma levels of empagliflozin were roughly 20% higher in subjects with mild and severe renal impairment as compared to subjects with normal renal function. Population pharmacokinetic analysis showed that the apparent oral clearance of empagliflozin decreased, with a decrease in eGFR leading to an increase in drug exposure. However, the fraction of empagliflozin that was excreted unchanged in urine, and urinary glucose excretion, declined with decrease in eGFR. Hepatic Impairment In subjects with mild, moderate, and severe hepatic impairment according to the Child-Pugh classification, AUC of empagliflozin increased by approximately 23%, 47%, and 75%, and C max increased by approximately 4%, 23%, and 48%, respectively, compared to subjects with normal hepatic function. Effects of Age, Body Mass Index, Gender, and Race Based on the population PK analysis, age, body mass index (BMI), gender and race (Asians versus primarily Whites) do not have a clinically meaningful effect on pharmacokinetics of empagliflozin [see Use in Specific Populations ( 8.5 )] . Pediatric Studies characterizing the pharmacokinetics of empagliflozin in pediatric patients have not been performed. Drug Interactions In vitro Assessment of Drug Interactions Empagliflozin does not inhibit, inactivate, or induce CYP450 isoforms. In vitro data suggest that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT1A3, UGT1A8, UGT1A9, and UGT2B7. Empagliflozin does not inhibit UGT1A1, UGT1A3, UGT1A8, UGT1A9, or UGT2B7. Therefore, no effect of empagliflozin is anticipated on concomitantly administered drugs that are substrates of the major CYP450 isoforms or UGT1A1, UGT1A3, UGT1A8, UGT1A9, or UGT2B7. The effect of UGT induction (e.g., induction by rifampicin or any other UGT enzyme inducer) on empagliflozin exposure has not been evaluated. Empagliflozin is a substrate for P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP), but it does not inhibit these efflux transporters at therapeutic doses.

GT2B7. The effect of UGT induction (e.g., induction by rifampicin or any other UGT enzyme inducer) on empagliflozin exposure has not been evaluated. Empagliflozin is a substrate for P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP), but it does not inhibit these efflux transporters at therapeutic doses. Based on in vitro studies, empagliflozin is considered unlikely to cause interactions with drugs that are P-gp substrates. Empagliflozin is a substrate of the human uptake transporters OAT3, OATP1B1, and OATP1B3, but not OAT1 and OCT2. Empagliflozin does not inhibit any of these human uptake transporters at clinically relevant plasma concentrations and, therefore, no effect of empagliflozin is anticipated on concomitantly administered drugs that are substrates of these uptake transporters. In vivo Assessment of Drug Interactions No dose adjustment of JARDIANCE is recommended when coadministered with commonly prescribed medicinal products based on results of the described pharmacokinetic studies. Empagliflozin pharmacokinetics were similar with and without coadministration of metformin, glimepiride, pioglitazone, sitagliptin, linagliptin, warfarin, verapamil, ramipril, and simvastatin in healthy volunteers and with or without coadministration of hydrochlorothiazide and torsemide in patients with type 2 diabetes (see Figure 1). The observed increases in overall exposure (AUC) of empagliflozin following coadministration with gemfibrozil, rifampicin, or probenecid are not clinically relevant. In subjects with normal renal function, coadministration of empagliflozin with probenecid resulted in a 30% decrease in the fraction of empagliflozin excreted in urine without any effect on 24-hour urinary glucose excretion. The relevance of this observation to patients with renal impairment is unknown. Figure 1 Effect of Various Medications on the Pharmacokinetics of Empagliflozin as Displayed as 90% Confidence Interval of Geometric Mean AUC and C max Ratios [reference lines indicate 100% (80% - 125%)] a empagliflozin, 50 mg, once daily; b empagliflozin, 25 mg, single dose; c empagliflozin, 25 mg, once daily; d empagliflozin, 10 mg, single dose Empagliflozin had no clinically relevant effect on the pharmacokinetics of metformin, glimepiride, pioglitazone, sitagliptin, linagliptin, warfarin, digoxin, ramipril, simvastatin, hydrochlorothiazide, torsemide, and oral contraceptives when coadministered in healthy volunteers (see Figure 2). Figure 2 Effect of Empagliflozin on the Pharmacokinetics of Various Medications as Displayed as 90% Confidence Interval of Geometric Mean AUC and C max Ratios [reference lines indicate 100% (80% - 125%)] a empagliflozin, 50 mg, once daily; b empagliflozin, 25 mg, once daily; c empagliflozin, 25 mg, single dose; d administered as simvastatin; e administered as warfarin racemic mixture; f administered as Microgynon ® ; g administered as ramipril figure-1 figure-2

12.1 Mechanism of Action Sodium-glucose co-transporter 2 (SGLT2) is the predominant transporter responsible for reabsorption of glucose from the glomerular filtrate back into the circulation. Empagliflozin is an inhibitor of SGLT2. By inhibiting SGLT2, empagliflozin reduces renal reabsorption of filtered glucose and lowers the renal threshold for glucose, and thereby increases urinary glucose excretion.

12.2 Pharmacodynamics Urinary Glucose Excretion In patients with type 2 diabetes, urinary glucose excretion increased immediately following a dose of JARDIANCE and was maintained at the end of a 4-week treatment period averaging at approximately 64 grams per day with 10 mg empagliflozin and 78 grams per day with 25 mg JARDIANCE once daily [see Clinical Studies ( 14 )]. Urinary Volume In a 5-day study, mean 24-hour urine volume increase from baseline was 341 mL on Day 1 and 135 mL on Day 5 of empagliflozin 25 mg once daily treatment. Cardiac Electrophysiology In a randomized, placebo-controlled, active-comparator, crossover study, 30 healthy subjects were administered a single oral dose of JARDIANCE 25 mg, JARDIANCE 200 mg (8 times the maximum dose), moxifloxacin, and placebo. No increase in QTc was observed with either 25 mg or 200 mg empagliflozin.

12.3 Pharmacokinetics Absorption The pharmacokinetics of empagliflozin has been characterized in healthy volunteers and patients with type 2 diabetes and no clinically relevant differences were noted between the two populations. After oral administration, peak plasma concentrations of empagliflozin were reached at 1.5 hours post-dose. Thereafter, plasma concentrations declined in a biphasic manner with a rapid distribution phase and a relatively slow terminal phase. The steady state mean plasma AUC and C max were 1870 nmol·h/L and 259 nmol/L, respectively, with 10 mg empagliflozin once daily treatment, and 4740 nmol·h/L and 687 nmol/L, respectively, with 25 mg empagliflozin once daily treatment. Systemic exposure of empagliflozin increased in a dose-proportional manner in the therapeutic dose range. The single-dose and steady-state pharmacokinetic parameters of empagliflozin were similar, suggesting linear pharmacokinetics with respect to time. Administration of 25 mg empagliflozin after intake of a high-fat and high-calorie meal resulted in slightly lower exposure; AUC decreased by approximately 16% and C max decreased by approximately 37%, compared to fasted condition. The observed effect of food on empagliflozin pharmacokinetics was not considered clinically relevant and empagliflozin may be administered with or without food. Distribution The apparent steady-state volume of distribution was estimated to be 73.8 L based on a population pharmacokinetic analysis. Following administration of an oral [ 14 C]-empagliflozin solution to healthy subjects, the red blood cell partitioning was approximately 36.8% and plasma protein binding was 86.2%. Metabolism No major metabolites of empagliflozin were detected in human plasma and the most abundant metabolites were three glucuronide conjugates (2-O-, 3-O-, and 6-O-glucuronide). Systemic exposure of each metabolite was less than 10% of total drug-related material. In vitro studies suggested that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT2B7, UGT1A3, UGT1A8, and UGT1A9. Elimination The apparent terminal elimination half-life of empagliflozin was estimated to be 12.4 h and apparent oral clearance was 10.6 L/h based on the population pharmacokinetic analysis. Following once-daily dosing, up to 22% accumulation, with respect to plasma AUC, was observed at steady-state, which was consistent with empagliflozin half-life. Following administration of an oral [ 14 C]-empagliflozin solution to healthy subjects, approximately 95.6% of the drug-related radioactivity was eliminated in feces (41.2%) or urine (54.4%). The majority of drug-related radioactivity recovered in feces was unchanged parent drug and approximately half of drug-related radioactivity excreted in urine was unchanged parent drug. Specific Populations Renal Impairment In patients with mild (eGFR: 60 to less than 90 mL/min/1.73 m 2 ), moderate (eGFR: 30 to less than 60 mL/min/1.73 m 2 ), and severe (eGFR: less than 30 mL/min/1.73 m 2 ) renal impairment and subjects with kidney failure/end stage renal disease (ESRD) patients, AUC of empagliflozin increased by approximately 18%, 20%, 66%, and 48%, respectively, compared to subjects with normal renal function. Peak plasma levels of empagliflozin were similar in subjects with moderate renal impairment and kidney failure/ESRD compared to patients with normal renal function.

ase (ESRD) patients, AUC of empagliflozin increased by approximately 18%, 20%, 66%, and 48%, respectively, compared to subjects with normal renal function. Peak plasma levels of empagliflozin were similar in subjects with moderate renal impairment and kidney failure/ESRD compared to patients with normal renal function. Peak plasma levels of empagliflozin were roughly 20% higher in subjects with mild and severe renal impairment as compared to subjects with normal renal function. Population pharmacokinetic analysis showed that the apparent oral clearance of empagliflozin decreased, with a decrease in eGFR leading to an increase in drug exposure. However, the fraction of empagliflozin that was excreted unchanged in urine, and urinary glucose excretion, declined with decrease in eGFR. Hepatic Impairment In subjects with mild, moderate, and severe hepatic impairment according to the Child-Pugh classification, AUC of empagliflozin increased by approximately 23%, 47%, and 75%, and C max increased by approximately 4%, 23%, and 48%, respectively, compared to subjects with normal hepatic function. Effects of Age, Body Mass Index, Gender, and Race Based on the population PK analysis, age, body mass index (BMI), gender and race (Asians versus primarily Whites) do not have a clinically meaningful effect on pharmacokinetics of empagliflozin [see Use in Specific Populations ( 8.5 )] . Pediatric Studies characterizing the pharmacokinetics of empagliflozin in pediatric patients have not been performed. Drug Interactions In vitro Assessment of Drug Interactions Empagliflozin does not inhibit, inactivate, or induce CYP450 isoforms. In vitro data suggest that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT1A3, UGT1A8, UGT1A9, and UGT2B7. Empagliflozin does not inhibit UGT1A1, UGT1A3, UGT1A8, UGT1A9, or UGT2B7. Therefore, no effect of empagliflozin is anticipated on concomitantly administered drugs that are substrates of the major CYP450 isoforms or UGT1A1, UGT1A3, UGT1A8, UGT1A9, or UGT2B7. The effect of UGT induction (e.g., induction by rifampicin or any other UGT enzyme inducer) on empagliflozin exposure has not been evaluated. Empagliflozin is a substrate for P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP), but it does not inhibit these efflux transporters at therapeutic doses. Based on in vitro studies, empagliflozin is considered unlikely to cause interactions with drugs that are P-gp substrates. Empagliflozin is a substrate of the human uptake transporters OAT3, OATP1B1, and OATP1B3, but not OAT1 and OCT2. Empagliflozin does not inhibit any of these human uptake transporters at clinically relevant plasma concentrations and, therefore, no effect of empagliflozin is anticipated on concomitantly administered drugs that are substrates of these uptake transporters. In vivo Assessment of Drug Interactions No dose adjustment of JARDIANCE is recommended when coadministered with commonly prescribed medicinal products based on results of the described pharmacokinetic studies. Empagliflozin pharmacokinetics were similar with and without coadministration of metformin, glimepiride, pioglitazone, sitagliptin, linagliptin, warfarin, verapamil, ramipril, and simvastatin in healthy volunteers and with or without coadministration of hydrochlorothiazide and torsemide in patients with type 2 diabetes (see Figure 1). The observed increases in overall exposure (AUC) of empagliflozin following coadministration with gemfibrozil, rifampicin, or probenecid are not clinically relevant.

mvastatin in healthy volunteers and with or without coadministration of hydrochlorothiazide and torsemide in patients with type 2 diabetes (see Figure 1). The observed increases in overall exposure (AUC) of empagliflozin following coadministration with gemfibrozil, rifampicin, or probenecid are not clinically relevant. In subjects with normal renal function, coadministration of empagliflozin with probenecid resulted in a 30% decrease in the fraction of empagliflozin excreted in urine without any effect on 24-hour urinary glucose excretion. The relevance of this observation to patients with renal impairment is unknown. Figure 1 Effect of Various Medications on the Pharmacokinetics of Empagliflozin as Displayed as 90% Confidence Interval of Geometric Mean AUC and C max Ratios [reference lines indicate 100% (80% - 125%)] a empagliflozin, 50 mg, once daily; b empagliflozin, 25 mg, single dose; c empagliflozin, 25 mg, once daily; d empagliflozin, 10 mg, single dose Empagliflozin had no clinically relevant effect on the pharmacokinetics of metformin, glimepiride, pioglitazone, sitagliptin, linagliptin, warfarin, digoxin, ramipril, simvastatin, hydrochlorothiazide, torsemide, and oral contraceptives when coadministered in healthy volunteers (see Figure 2). Figure 2 Effect of Empagliflozin on the Pharmacokinetics of Various Medications as Displayed as 90% Confidence Interval of Geometric Mean AUC and C max Ratios [reference lines indicate 100% (80% - 125%)] a empagliflozin, 50 mg, once daily; b empagliflozin, 25 mg, once daily; c empagliflozin, 25 mg, single dose; d administered as simvastatin; e administered as warfarin racemic mixture; f administered as Microgynon ® ; g administered as ramipril figure-1 figure-2

13 NONCLINICAL TOXICOLOGY 13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility Carcinogenesis Carcinogenesis was evaluated in 2-year studies conducted in CD-1 mice and Wistar rats. Empagliflozin did not increase the incidence of tumors in female rats dosed at 100, 300, or 700 mg/kg/day (up to 72 times the exposure from the maximum clinical dose of 25 mg). In male rats, hemangiomas of the mesenteric lymph node were increased significantly at 700 mg/kg/day or approximately 42 times the exposure from a 25 mg clinical dose. Empagliflozin did not increase the incidence of tumors in female mice dosed at 100, 300, or 1000 mg/kg/day (up to 62 times the exposure from a 25 mg clinical dose). Renal tubule adenomas and carcinomas were observed in male mice at 1000 mg/kg/day, which is approximately 45 times the exposure of the maximum clinical dose of 25 mg. These tumors may be associated with a metabolic pathway predominantly present in the male mouse kidney. Mutagenesis Empagliflozin was not mutagenic or clastogenic with or without metabolic activation in the in vitro Ames bacterial mutagenicity assay, the in vitro L5178Y tk +/- mouse lymphoma cell assay, and an in vivo micronucleus assay in rats. Impairment of Fertility Empagliflozin had no effects on mating, fertility or early embryonic development in treated male or female rats up to the high dose of 700 mg/kg/day (approximately 155 times the 25 mg clinical dose in males and females, respectively).

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility Carcinogenesis Carcinogenesis was evaluated in 2-year studies conducted in CD-1 mice and Wistar rats. Empagliflozin did not increase the incidence of tumors in female rats dosed at 100, 300, or 700 mg/kg/day (up to 72 times the exposure from the maximum clinical dose of 25 mg). In male rats, hemangiomas of the mesenteric lymph node were increased significantly at 700 mg/kg/day or approximately 42 times the exposure from a 25 mg clinical dose. Empagliflozin did not increase the incidence of tumors in female mice dosed at 100, 300, or 1000 mg/kg/day (up to 62 times the exposure from a 25 mg clinical dose). Renal tubule adenomas and carcinomas were observed in male mice at 1000 mg/kg/day, which is approximately 45 times the exposure of the maximum clinical dose of 25 mg. These tumors may be associated with a metabolic pathway predominantly present in the male mouse kidney. Mutagenesis Empagliflozin was not mutagenic or clastogenic with or without metabolic activation in the in vitro Ames bacterial mutagenicity assay, the in vitro L5178Y tk +/- mouse lymphoma cell assay, and an in vivo micronucleus assay in rats. Impairment of Fertility Empagliflozin had no effects on mating, fertility or early embryonic development in treated male or female rats up to the high dose of 700 mg/kg/day (approximately 155 times the 25 mg clinical dose in males and females, respectively).

14 CLINICAL STUDIES 14.1 Glycemic Control JARDIANCE has been studied as monotherapy and in combination with metformin, sulfonylurea, pioglitazone, linagliptin, and insulin. JARDIANCE has also been studied in patients with type 2 diabetes with mild or moderate renal impairment. In patients with type 2 diabetes, treatment with JARDIANCE reduced hemoglobin A1c (HbA1c), compared to placebo. The reduction in HbA1c for JARDIANCE compared with placebo was observed across subgroups including gender, race, geographic region, baseline BMI and duration of disease. Monotherapy A total of 986 patients with type 2 diabetes participated in a double-blind, placebo-controlled study to evaluate the efficacy and safety of JARDIANCE monotherapy. Treatment-naïve patients with inadequately controlled type 2 diabetes entered an open-label placebo run-in for 2 weeks. At the end of the run-in period, patients who remained inadequately controlled and had an HbA1c between 7 and 10% were randomized to placebo, JARDIANCE 10 mg, JARDIANCE 25 mg, or a reference comparator. At Week 24, treatment with JARDIANCE 10 mg or 25 mg daily provided statistically significant reductions in HbA1c (p-value <0.0001), fasting plasma glucose (FPG), and body weight compared with placebo (see Table 4 and Figure 3). Table 4 Results at Week 24 From a Placebo-Controlled Monotherapy Study of JARDIANCE a Modified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 24. At Week 24, 9.4%, 9.4%, and 30.7% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA derived p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) c FPG (mg/dL); for JARDIANCE 10 mg, n=223, for JARDIANCE 25 mg, n=223, and for placebo, n=226 JARDIANCE 10 mg N=224 JARDIANCE 25 mg N=224 Placebo N=228 HbA1c (%) a Baseline (mean) 7.9 7.9 7.9 Change from baseline (adjusted mean) -0.7 -0.8 0.1 Difference from placebo (adjusted mean) (97.5% CI) -0.7 b (-0.9, -0.6) -0.9 b (-1.0, -0.7) -- Patients [n (%)] achieving HbA1c <7% 72 (35%) 88 (44%) 25 (12%) FPG (mg/dL) c Baseline (mean) 153 153 155 Change from baseline (adjusted mean) -19 -25 12 Difference from placebo (adjusted mean) (95% CI) -31 (-37, -26) -36 (-42, -31) -- Body Weight Baseline (mean) in kg 78 78 78 % change from baseline (adjusted mean) -2.8 -3.2 -0.4 Difference from placebo (adjusted mean) (95% CI) -2.5 b (-3.1, -1.9) -2.8 b (-3.4, -2.2) -- Figure 3 Adjusted Mean HbA1c Change at Each Time Point (Completers) and at Week 24 (mITT Population) - LOCF At Week 24, the systolic blood pressure was statistically significantly reduced compared to placebo by -2.6 mmHg (placebo-adjusted, p-value=0.0231) in patients randomized to 10 mg of JARDIANCE and by -3.4 mmHg (placebo-corrected, p-value=0.0028) in patients randomized to 25 mg of JARDIANCE. Add-On Combination Therapy with Metformin A total of 637 patients with type 2 diabetes participated in a double-blind, placebo-controlled study to evaluate the efficacy and safety of JARDIANCE in combination with metformin. Patients with type 2 diabetes inadequately controlled on at least 1500 mg of metformin per day entered an open-label 2 week placebo run-in.

total of 637 patients with type 2 diabetes participated in a double-blind, placebo-controlled study to evaluate the efficacy and safety of JARDIANCE in combination with metformin. Patients with type 2 diabetes inadequately controlled on at least 1500 mg of metformin per day entered an open-label 2 week placebo run-in. At the end of the run-in period, patients who remained inadequately controlled and had an HbA1c between 7 and 10% were randomized to placebo, JARDIANCE 10 mg, or JARDIANCE 25 mg. At Week 24, treatment with JARDIANCE 10 mg or 25 mg daily provided statistically significant reductions in HbA1c (p-value <0.0001), FPG, and body weight compared with placebo (see Table 5). Table 5 Results at Week 24 From a Placebo-Controlled Study for JARDIANCE used in Combination with Metformin a Modified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 24. At Week 24, 9.7%, 14.1%, and 24.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) c FPG (mg/dL); for JARDIANCE 10 mg, n=216, for JARDIANCE 25 mg, n=213, and for placebo, n=207 JARDIANCE 10 mg + Metformin N=217 JARDIANCE 25 mg + Metformin N=213 Placebo + Metformin N=207 HbA1c (%) a Baseline (mean) 7.9 7.9 7.9 Change from baseline (adjusted mean) -0.7 -0.8 -0.1 Difference from placebo + metformin (adjusted mean) (95% CI) -0.6 b (-0.7, -0.4) -0.6 b (-0.8, -0.5) -- Patients [n (%)] achieving HbA1c <7% 75 (38%) 74 (39%) 23 (13%) FPG (mg/dL) c Baseline (mean) 155 149 156 Change from baseline (adjusted mean) -20 -22 6 Difference from placebo + metformin (adjusted mean) -26 -29 -- Body Weight Baseline mean in kg 82 82 80 % change from baseline (adjusted mean) -2.5 -2.9 -0.5 Difference from placebo (adjusted mean) (95% CI) -2.0 b (-2.6, -1.4) -2.5 b (-3.1, -1.9) -- At Week 24, the systolic blood pressure was statistically significantly reduced compared to placebo by -4.1 mmHg (placebo-corrected, p-value <0.0001) for JARDIANCE 10 mg and -4.8 mmHg (placebo-corrected, p-value <0.0001) for JARDIANCE 25 mg. Initial Combination Therapy with Metformin A total of 1364 patients with type 2 diabetes participated in a double-blind, randomized, active-controlled study to evaluate the efficacy and safety of JARDIANCE in combination with metformin as initial therapy compared to the corresponding individual components. Treatment-naïve patients with inadequately controlled type 2 diabetes entered an open-label placebo run-in for 2 weeks. At the end of the run-in period, patients who remained inadequately controlled and had an HbA1c between 7 and 10.5% were randomized to one of 8 active-treatment arms: JARDIANCE 10 mg or 25 mg; metformin 1000 mg, or 2000 mg; JARDIANCE 10 mg in combination with 1000 mg or 2000 mg metformin; or JARDIANCE 25 mg in combination with 1000 mg or 2000 mg metformin. At Week 24, initial therapy of JARDIANCE in combination with metformin provided statistically significant reductions in HbA1c (p-value <0.01) compared to the individual components (see Table 6). Table 6 Glycemic Parameters at 24 Weeks in a Study Comparing JARDIANCE and Metformin to the Individual Components as Initial Therapy a Metformin total daily dose, administered in two equally divided doses per day. b p-value ≤0.0062 (modified intent to treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c).

ormin to the Individual Components as Initial Therapy a Metformin total daily dose, administered in two equally divided doses per day. b p-value ≤0.0062 (modified intent to treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c). c p-value ≤0.0056 (modified intent to treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c). JARDIANCE 10 mg + Metformin 1000 mg a N=161 JARDIANCE 10 mg + Metformin 2000 mg a N=167 JARDIANCE 25 mg + Metformin 1000 mg a N=165 JARDIANCE 25 mg + Metformin 2000 mg a N=169 JARDIANCE 10 mg N=169 JARDIANCE 25 mg N=163 Metformin 1000 mg a N=167 Metformin 2000 mg a N=162 HbA1c (%) Baseline (mean) 8.7 8.7 8.8 8.7 8.6 8.9 8.7 8.6 Change from baseline (adjusted mean) -2.0 -2.1 -1.9 -2.1 -1.4 -1.4 -1.2 -1.8 Comparison vs JARDIANCE (adjusted mean) (95% CI) -0.6 b (-0.9, -0.4) -0.7 b (-1.0, -0.5) -0.6 c (-0.8, -0.3) -0.7 c (-1.0, -0.5) -- -- -- -- Comparison vs metformin (adjusted mean) (95% CI) -0.8 b (-1.0, -0.6) -0.3 b (-0.6, -0.1) -0.8 c (-1.0, -0.5) -0.3 c (-0.6, -0.1) -- -- -- -- Add-On Combination Therapy with Metformin and Sulfonylurea A total of 666 patients with type 2 diabetes participated in a double-blind, placebo-controlled study to evaluate the efficacy and safety of JARDIANCE in combination with metformin plus a sulfonylurea. Patients with inadequately controlled type 2 diabetes on at least 1500 mg per day of metformin and on a sulfonylurea, entered a 2 week open-label placebo run-in. At the end of the run-in, patients who remained inadequately controlled and had an HbA1c between 7% and 10% were randomized to placebo, JARDIANCE 10 mg, or JARDIANCE 25 mg. Treatment with JARDIANCE 10 mg or 25 mg daily provided statistically significant reductions in HbA1c (p-value <0.0001), FPG, and body weight compared with placebo (see Table 7). Table 7 Results at Week 24 from a Placebo-Controlled Study for JARDIANCE in Combination with Metformin and Sulfonylurea a Modified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 24. At Week 24, 17.8%, 16.7%, and 25.3% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) c FPG (mg/dL); for JARDIANCE 10 mg, n=225, for JARDIANCE 25 mg, n=215, for placebo, n=224 JARDIANCE 10 mg + Metformin + SU N=225 JARDIANCE 25 mg + Metformin + SU N=216 Placebo + Metformin + SU N=225 HbA1c (%) a Baseline (mean) 8.1 8.1 8.2 Change from baseline (adjusted mean) -0.8 -0.8 -0.2 Difference from placebo (adjusted mean) (95% CI) -0.6 b (-0.8, -0.5) -0.6 b (-0.7, -0.4) -- Patients [n (%)] achieving HbA1c <7% 55 (26%) 65 (32%) 20 (9%) FPG (mg/dL) c Baseline (mean) 151 156 152 Change from baseline (adjusted mean) -23 -23 6 Difference from placebo (adjusted mean) -29 -29 -- Body Weight Baseline mean in kg 77 78 76 % change from baseline (adjusted mean) -2.9 -3.2 -0.5 Difference from placebo (adjusted mean) (95% CI) -2.4 b (-3.0, -1.8) -2.7 b (-3.3, -2.1) -- In Combination with Linagliptin as Add-On to Metformin Therapy A total of 686 patients with type 2 diabetes participated in a double-blind, active-controlled study to evaluate the efficacy and safety of JARDIANCE 10 mg or 25 mg in combination with linagliptin 5 mg compared to the individual components. Patients with type 2 diabetes inadequately controlled on at least 1500 mg of metformin per day entered a single-blind placebo run-in period for 2 weeks.

nd, active-controlled study to evaluate the efficacy and safety of JARDIANCE 10 mg or 25 mg in combination with linagliptin 5 mg compared to the individual components. Patients with type 2 diabetes inadequately controlled on at least 1500 mg of metformin per day entered a single-blind placebo run-in period for 2 weeks. At the end of the run-in period, patients who remained inadequately controlled and had an HbA1c between 7 and 10.5% were randomized 1:1:1:1:1 to one of 5 active-treatment arms of JARDIANCE 10 mg or 25 mg, linagliptin 5 mg, or linagliptin 5 mg in combination with 10 mg or 25 mg JARDIANCE as a fixed dose combination tablet. At Week 24, JARDIANCE 10 mg or 25 mg used in combination with linagliptin 5 mg provided statistically significant improvement in HbA1c (p-value <0.0001) and FPG (p-value <0.001) compared to the individual components in patients who had been inadequately controlled on metformin. Treatment with JARDIANCE/linagliptin 25 mg/5 mg or JARDIANCE/linagliptin 10 mg/5 mg daily also resulted in a statistically significant reduction in body weight compared to linagliptin 5 mg (p-value <0.0001). There was no statistically significant difference in body weight compared to JARDIANCE alone. Active-Controlled Study versus Glimepiride in Combination with Metformin The efficacy of JARDIANCE was evaluated in a double-blind, glimepiride-controlled, study in 1545 patients with type 2 diabetes with insufficient glycemic control despite metformin therapy. Patients with inadequate glycemic control and an HbA1c between 7% and 10% after a 2-week run-in period were randomized to glimepiride or JARDIANCE 25 mg. At Week 52, JARDIANCE 25 mg and glimepiride lowered HbA1c and FPG (see Table 8, Figure 4). The difference in observed effect size between JARDIANCE 25 mg and glimepiride excluded the pre-specified non-inferiority margin of 0.3%. The mean daily dose of glimepiride was 2.7 mg and the maximal approved dose in the United States is 8 mg per day. Table 8 Results at Week 52 from an Active-Controlled Study Comparing JARDIANCE to Glimepiride as Add-On Therapy in Patients Inadequately Controlled on Metformin a Modified intent to treat population. Last observation on study (LOCF) was used to impute data missing at Week 52. At Week 52, data was imputed for 15.3% and 21.9% of patients randomized to JARDIANCE 25 mg and glimepiride, respectively. b Non-inferior, ANCOVA model p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region) c ANCOVA p-value <0.0001 (Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) d FPG (mg/dL); for JARDIANCE 25 mg, n=764, for placebo, n=779 JARDIANCE 25 mg + Metformin N=765 Glimepiride + Metformin N=780 HbA1c (%) a Baseline (mean) 7.9 7.9 Change from baseline (adjusted mean) -0.7 -0.7 Difference from glimepiride (adjusted mean) (97.5% CI) -0.07 b (-0.15, 0.01) -- FPG (mg/dL) d Baseline (mean) 150 150 Change from baseline (adjusted mean) -19 -9 Difference from glimepiride (adjusted mean) -11 -- Body Weight Baseline mean in kg 82.5 83 % change from baseline (adjusted mean) -3.9 2.0 Difference from glimepiride (adjusted mean) (95% CI) -5.9 c (-6.3, -5.5) -- Figure 4 Adjusted mean HbA1c Change at Each Time Point (Completers) and at Week 52 (mITT Population) - LOCF At Week 52, the adjusted mean change from baseline in systolic blood pressure was -3.6 mmHg, compared to 2.2 mmHg for glimepiride. The differences between treatment groups for systolic blood pressure was statistically significant (p-value <0.0001). At Week 104, the adjusted mean change from baseline in HbA1c was -0.75% for JARDIANCE 25 mg and -0.66% for glimepiride.

ne in systolic blood pressure was -3.6 mmHg, compared to 2.2 mmHg for glimepiride. The differences between treatment groups for systolic blood pressure was statistically significant (p-value <0.0001). At Week 104, the adjusted mean change from baseline in HbA1c was -0.75% for JARDIANCE 25 mg and -0.66% for glimepiride. The adjusted mean treatment difference was -0.09% with a 97.5% confidence interval of (-0.32%, 0.15%), excluding the pre-specified non-inferiority margin of 0.3%. The mean daily dose of glimepiride was 2.7 mg and the maximal approved dose in the United States is 8 mg per day. The Week 104 analysis included data with and without concomitant glycemic rescue medication, as well as off-treatment data. Missing data for patients not providing any information at the visit were imputed based on the observed off-treatment data. In this multiple imputation analysis, 13.9% of the data were imputed for JARDIANCE 25 mg and 12.9% for glimepiride. At Week 104, JARDIANCE 25 mg daily resulted in a statistically significant difference in change from baseline for body weight compared to glimepiride (-3.1 kg for JARDIANCE 25 mg vs. +1.3 kg for glimepiride; ANCOVA-LOCF, p-value <0.0001). Add-On Combination Therapy with Pioglitazone with or without Metformin A total of 498 patients with type 2 diabetes participated in a double-blind, placebo-controlled study to evaluate the efficacy and safety of JARDIANCE in combination with pioglitazone, with or without metformin. Patients with inadequately controlled type 2 diabetes on metformin at a dose of at least 1500 mg per day and pioglitazone at a dose of at least 30 mg per day were placed into an open-label placebo run-in for 2 weeks. Patients with inadequate glycemic control and an HbA1c between 7% and 10% after the run-in period were randomized to placebo, JARDIANCE 10 mg, or JARDIANCE 25 mg. Treatment with JARDIANCE 10 mg or 25 mg daily resulted in statistically significant reductions in HbA1c (p-value <0.0001), FPG, and body weight compared with placebo (see Table 9). Table 9 Results of Placebo-Controlled Study for JARDIANCE in Combination Therapy with Pioglitazone a Modified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 24. At Week 24, 10.9%, 8.3%, and 20.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and background medication. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) c FPG (mg/dL); for JARDIANCE 10 mg, n=163 JARDIANCE 10 mg + Pioglitazone N=165 JARDIANCE 25 mg + Pioglitazone N=168 Placebo + Pioglitazone N=165 HbA1c (%) a Baseline (mean) 8.1 8.1 8.2 Change from baseline (adjusted mean) -0.6 -0.7 -0.1 Difference from placebo + pioglitazone (adjusted mean) (95% CI) -0.5 b (-0.7, -0.3) -0.6 b (-0.8, -0.4) -- Patients [n (%)] achieving HbA1c <7% 36 (24%) 48 (30%) 12 (8%) FPG (mg/dL) c Baseline (mean) 152 152 152 Change from baseline (adjusted mean) -17 -22 7 Difference from placebo + pioglitazone (adjusted mean) (97.5% CI) -23 b (-31.8, -15.2) -28 b (-36.7, -20.2) -- Body Weight Baseline mean in kg 78 79 78 % change from baseline (adjusted mean) -2.0 -1.8 0.6 Difference from placebo (adjusted mean) (95% CI) -2.6 b (-3.4, -1.8) -2.4 b (-3.2, -1.6) -- Add-On Combination with Insulin with or without Metformin and/or Sulfonylureas A total of 494 patients with type 2 diabetes inadequately controlled on insulin, or insulin in combination with oral drugs participated in a double-blind, placebo-controlled study to evaluate the efficacy of JARDIANCE as add-on therapy to insulin over 78 weeks.

ith Insulin with or without Metformin and/or Sulfonylureas A total of 494 patients with type 2 diabetes inadequately controlled on insulin, or insulin in combination with oral drugs participated in a double-blind, placebo-controlled study to evaluate the efficacy of JARDIANCE as add-on therapy to insulin over 78 weeks. Patients entered a 2-week placebo run-in period on basal insulin (e.g., insulin glargine, insulin detemir, or NPH insulin) with or without metformin and/or sulfonylurea background therapy. Following the run-in period, patients with inadequate glycemic control were randomized to the addition of JARDIANCE 10 mg, JARDIANCE 25 mg, or placebo. Patients were maintained on a stable dose of insulin prior to enrollment, during the run-in period, and during the first 18 weeks of treatment. For the remaining 60 weeks, insulin could be adjusted. The mean total daily insulin dose at baseline for JARDIANCE 10 mg, 25 mg, and placebo was 45 IU, 48 IU, and 48 IU, respectively. JARDIANCE used in combination with insulin (with or without metformin and/or sulfonylurea) provided statistically significant reductions in HbA1c and FPG compared to placebo after both 18 and 78 weeks of treatment (see Table 10). JARDIANCE 10 mg or 25 mg daily also resulted in statistically significantly greater percent body weight reduction compared to placebo. Table 10 Results at Week 18 and 78 for a Placebo-Controlled Study for JARDIANCE in Combination with Insulin a Modified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 18 and 78. At Week 18, 21.3%, 30.3%, and 21.8% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. At Week 78, 32.5%, 38.1% and 42.4% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, and region; FPG: MMRM model includes baseline FPG, baseline HbA1c, treatment, region, visit and visit by treatment interaction. Body weight: MMRM model includes baseline body weight, baseline HbA1c, treatment, region, visit and visit by treatment interaction. c p-value=0.0049 d p-value=0.0052 e p-value=0.0463 18 weeks (no insulin adjustment) 78 weeks (adjustable insulin dose after 18 weeks) JARDIANCE 10 mg + Insulin N=169 JARDIANCE 25 mg + Insulin N=155 Placebo + Insulin N=170 JARDIANCE 10 mg + Insulin N=169 JARDIANCE 25 mg + Insulin N=155 Placebo + Insulin N=170 HbA1c (%) a Baseline (mean) 8.3 8.3 8.2 8.3 8.3 8.2 Change from baseline (adjusted mean) -0.6 -0.7 0 -0.4 -0.6 0.1 Difference from placebo (adjusted mean) (97.5% CI) -0.6 b (-0.8, -0.4) -0.7 b (-0.9, -0.5) -- -0.5 b (-0.7, -0.3) -0.7 b (-0.9, -0.5) -- Patients (%) achieving HbA1c <7% 18.0 19.5 5.5 12.0 17.5 6.7 FPG (mg/dL) Baseline (mean) 138 146 142 138 146 142 Change from baseline (adjusted mean, SE) -17.9 (3.2) -19.1 (3.3) 10.4 (3.1) -10.1 (3.2) -15.2 (3.4) 2.8 (3.2) Difference from placebo (adjusted mean) (95% CI) -28.2 b (-37.0, -19.5) -29.5 b (-38.4, -20.6) -- -12.9 c (-21.9, 3.9) -17.9 b (-27.0, -8.8) -- Body Weight Baseline mean in kg 92 95 90 92 95 90 % change from baseline (adjusted mean) -1.8 -1.4 -0.1 -2.4 -2.4 0.7 Difference from placebo (adjusted mean) (95% CI) -1.7 d (-3.0, -0.5) -1.3 e (-2.5, -0.0) -- -3.0 b (-4.4, -1.7) -3.0 b (-4.4, -1.6) -- Add-on Combination with MDI Insulin with or without Metformin A total of 563 patients with type 2 diabetes inadequately controlled on multiple daily injections (MDI) of insulin (total daily dose >60 IU), alone or in combination with metformin, participated in a double-blind, placebo-controlled study to evaluate the efficacy of JARDIANCE as add-on therapy to MDI insulin over 18 weeks.

tal of 563 patients with type 2 diabetes inadequately controlled on multiple daily injections (MDI) of insulin (total daily dose >60 IU), alone or in combination with metformin, participated in a double-blind, placebo-controlled study to evaluate the efficacy of JARDIANCE as add-on therapy to MDI insulin over 18 weeks. Patients entered a 2-week placebo run-in period on MDI insulin with or without metformin background therapy. Following the run-in period, patients with inadequate glycemic control were randomized to the addition of JARDIANCE 10 mg, JARDIANCE 25 mg, or placebo. Patients were maintained on a stable dose of insulin prior to enrollment, during the run-in period, and during the first 18 weeks of treatment. The mean total daily insulin dose at baseline for JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo was 88.6 IU, 90.4 IU, and 89.9 IU, respectively. JARDIANCE 10 mg or 25 mg daily used in combination with MDI insulin (with or without metformin) provided statistically significant reductions in HbA1c compared to placebo after 18 weeks of treatment (see Table 11). Table 11 Results at Week 18 for a Placebo-Controlled Study for JARDIANCE in Combination with Insulin and with or without Metformin a Modified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 18. At Week 18, 23.7%, 22.8% and 23.4% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. b ANCOVA p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, geographical region, and background medication). JARDIANCE 10 mg + Insulin +/- Metformin N=186 JARDIANCE 25 mg + Insulin +/- Metformin N=189 Placebo + Insulin +/- Metformin N=188 HbA1c (%) a Baseline (mean) 8.4 8.3 8.3 Change from baseline (adjusted mean) -0.9 -1.0 -0.5 Difference from placebo (adjusted mean) (95% CI) -0.4 b (-0.6, -0.3) -0.5 b (-0.7, -0.4) -- During an extension period with treatment for up to 52 weeks, insulin could be adjusted to achieve defined glucose target levels. The change from baseline in HbA1c was maintained from 18 to 52 weeks with both JARDIANCE 10 mg and 25 mg. After 52 weeks, JARDIANCE 10 mg or 25 mg daily resulted in statistically greater percent body weight reduction compared to placebo (p-value <0.0001). The mean change in body weight from baseline was -1.95 kg for JARDIANCE 10 mg, and -2.04 kg for JARDIANCE 25 mg. Renal Impairment A total of 738 patients with type 2 diabetes and a baseline eGFR less than 90 mL/min/1.73 m 2 participated in a randomized, double-blind, placebo-controlled, parallel-group to evaluate the efficacy and safety of JARDIANCE in patients with type 2 diabetes and renal impairment. The trial population comprised of 290 patients with mild renal impairment (eGFR 60 to less than 90 mL/min/1.73 m 2 ), 374 patients with moderate renal impairment (eGFR 30 to less than 60 mL/min/1.73 m 2 ), and 74 with severe renal impairment (eGFR less than 30 mL/min/1.73 m 2 ). A total of 194 patients with moderate renal impairment had a baseline eGFR of 30 to less than 45 mL/min/1.73 m 2 and 180 patients a baseline eGFR of 45 to less than 60 mL/min/1.73 m 2 . At Week 24, JARDIANCE 25 mg provided statistically significant reduction in HbA1c relative to placebo in patients with mild to moderate renal impairment (see Table 12). A statistically significant reduction relative to placebo was also observed with JARDIANCE 25 mg in patients with either mild [-0.7 (95% CI: -0.9, -0.5)] or moderate [-0.4 (95% CI: -0.6, -0.3)] renal impairment and with JARDIANCE 10 mg in patients with mild [-0.5 (95% CI: -0.7, -0.3)] renal impairment. The glucose lowering efficacy of JARDIANCE 25 mg decreased with decreasing level of renal function in the mild to moderate range.

either mild [-0.7 (95% CI: -0.9, -0.5)] or moderate [-0.4 (95% CI: -0.6, -0.3)] renal impairment and with JARDIANCE 10 mg in patients with mild [-0.5 (95% CI: -0.7, -0.3)] renal impairment. The glucose lowering efficacy of JARDIANCE 25 mg decreased with decreasing level of renal function in the mild to moderate range. Least square mean Hb1Ac changes at 24 weeks were -0.6%, -0.5%, and -0.2% for those with a baseline eGFR of 60 to less than 90 mL/min/1.73 m 2 , 45 to less than 60 mL/min/1.73 m 2 , and 30 to less than 45 mL/min/1.73 m 2 , respectively [see Dosage and Administration ( 2 ) and Use in Specific Populations ( 8.6 )] . For placebo, least square mean HbA1c changes at 24 weeks were 0.1%, -0.1%, and 0.2% for patients with a baseline eGFR of 60 to less than 90 mL/min/1.73 m 2 , 45 to less than 60 mL/min/1.73 m 2 , and 30 to less than 45 mL/min/1.73 m 2 , respectively. Table 12 Results at Week 24 (LOCF) of Placebo-Controlled Study for JARDIANCE in Patients with Type 2 Diabetes and Renal Impairment a p-value <0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and background medication) b eGFR 30 to less than 90 mL/min/1.73 m 2 - Modified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 24. At Week 24, 24.6% and 26.2% was imputed for patients randomized to JARDIANCE 25 mg and placebo, respectively. Mild and Moderate Impairment b JARDIANCE 25 mg HbA1c Number of patients n=284 Comparison vs placebo (adjusted mean) (95% CI) -0.5 a (-0.6, -0.4) For patients with severe renal impairment, the analyses of changes in HbA1c and FPG showed no discernible treatment effect of JARDIANCE 25 mg compared to placebo [see Dosage and Administration ( 2.2 ) and Use in Specific Populations ( 8.6 )] . Figure 3 Figure 4 14.2 Cardiovascular Outcomes in Patients with Type 2 Diabetes Mellitus and Atherosclerotic Cardiovascular Disease The effect of JARDIANCE on cardiovascular risk in adult patients with type 2 diabetes and established, stable, atherosclerotic cardiovascular disease was evaluated in the EMPA-REG OUTCOME study, a multicenter, multi-national, randomized, double-blind parallel group trial. The study compared the risk of experiencing a major adverse cardiovascular event (MACE) between JARDIANCE and placebo when these were added to and used concomitantly with standard of care treatments for diabetes and atherosclerotic cardiovascular disease. Coadministered antidiabetic medications were to be kept stable for the first 12 weeks of the trial. Thereafter, antidiabetic and atherosclerotic therapies could be adjusted, at the discretion of investigators, to ensure participants were treated according to the standard care for these diseases. A total of 7020 patients were treated (JARDIANCE 10 mg = 2345; JARDIANCE 25 mg = 2342; placebo = 2333) and followed for a median of 3.1 years. Approximately 72% of the study population was Caucasian, 22% was Asian, and 5% was Black. The mean age was 63 years and approximately 72% were male. All patients in the study had inadequately controlled type 2 diabetes mellitus at baseline (HbA1c greater than or equal to 7%). The mean HbA1c at baseline was 8.1% and 57% of participants had had diabetes for more than 10 years. Approximately 31%, 22% and 20% reported a past history of neuropathy, retinopathy and nephropathy to investigators respectively and the mean eGFR was 74 mL/min/1.73 m 2 . At baseline, patients were treated with one (~30%) or more (~70%) antidiabetic medications including metformin (74%), insulin (48%), and sulfonylurea (43%).

mately 31%, 22% and 20% reported a past history of neuropathy, retinopathy and nephropathy to investigators respectively and the mean eGFR was 74 mL/min/1.73 m 2 . At baseline, patients were treated with one (~30%) or more (~70%) antidiabetic medications including metformin (74%), insulin (48%), and sulfonylurea (43%). All patients had established atherosclerotic cardiovascular disease at baseline including one (82%) or more (18%) of the following; a documented history of coronary artery disease (76%), stroke (23%) or peripheral artery disease (21%). At baseline, the mean systolic blood pressure was 136 mmHg, the mean diastolic blood pressure was 76 mmHg, the mean LDL was 86 mg/dL, the mean HDL was 44 mg/dL, and the mean urinary albumin to creatinine ratio (UACR) was 175 mg/g. At baseline, approximately 81% of patients were treated with renin angiotensin system inhibitors, 65% with beta-blockers, 43% with diuretics, 77% with statins, and 86% with antiplatelet agents (mostly aspirin). The primary endpoint in EMPA-REG OUTCOME was the time to first occurrence of a Major Adverse Cardiac Event (MACE). A major adverse cardiac event was defined as occurrence of either a cardiovascular death or a nonfatal myocardial infarction (MI) or a nonfatal stroke. The statistical analysis plan had pre-specified that the 10 and 25 mg doses would be combined. A Cox proportional hazards model was used to test for non-inferiority against the pre-specified risk margin of 1.3 for the hazard ratio of MACE and superiority on MACE if non-inferiority was demonstrated. Type-1 error was controlled across multiples tests using a hierarchical testing strategy. JARDIANCE significantly reduced the risk of first occurrence of primary composite endpoint of cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke (HR: 0.86; 95% CI 0.74, 0.99). The treatment effect was due to a significant reduction in the risk of cardiovascular death in subjects randomized to empagliflozin (HR: 0.62; 95% CI 0.49, 0.77), with no change in the risk of non-fatal myocardial infarction or non-fatal stroke (see Table 13 and Figure 5 and 6). Results for the 10 mg and 25 mg empagliflozin doses were consistent with results for the combined dose groups. Table 13 Treatment Effect for the Primary Composite Endpoint, and its Components a a Treated set (patients who had received at least one dose of study drug) b p−value for superiority (2−sided) 0.04 c Total number of events Placebo N=2333 JARDIANCE N=4687 Hazard ratio vs placebo (95% CI) Composite of cardiovascular death, non-fatal myocardial infarction, non-fatal stroke (time to first occurrence) b 282 (12.1%) 490 (10.5%) 0.86 (0.74, 0.99) Non-fatal myocardial infarction c 121 (5.2%) 213 (4.5%) 0.87 (0.70, 1.09) Non-fatal stroke c 60 (2.6%) 150 (3.2%) 1.24 (0.92, 1.67) Cardiovascular death c 137 (5.9%) 172 (3.7%) 0.62 (0.49, 0.77) The efficacy of JARDIANCE on cardiovascular death was generally consistent across major demographic and disease subgroups. Vital status was obtained for 99.2% of subjects in the trial. A total of 463 deaths were recorded during the EMPA-REG OUTCOME trial. Most of these deaths were categorized as cardiovascular deaths. The non-cardiovascular deaths were only a small proportion of deaths, and were balanced between the treatment groups (2.1% in patients treated with JARDIANCE, and 2.4% of patients treated with placebo). Figure 5 Figure 6

<table ID="t11018722" border="0" width="100%"><caption>Table 4 Results at Week 24 From a Placebo-Controlled Monotherapy Study of JARDIANCE</caption><col valign="top" width="2.5%"/><col width="37.5%"/><col valign="top" width="20%"/><col valign="top" width="20%"/><col valign="top" width="20%"/><tfoot><tr><td colspan="5">^aModified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 24. At Week 24, 9.4%, 9.4%, and 30.7% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA derived p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region.

tudy (LOCF) was used to impute missing data at Week 24. At Week 24, 9.4%, 9.4%, and 30.7% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA derived p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) ^cFPG (mg/dL); for JARDIANCE 10 mg, n=223, for JARDIANCE 25 mg, n=223, and for placebo, n=226 </td></tr></tfoot><tbody><tr><td colspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">JARDIANCE 10 mg N=224 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">JARDIANCE 25 mg N=224 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">Placebo N=228 </content></td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">HbA1c (%) ^a</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">7.9</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">7.9</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">7.9</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.7</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.8</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">0.1</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean) (97.5% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.7 ^b(-0.9, -0.6) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.9 ^b(-1.0, -0.7) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Patients [n (%)] achieving HbA1c &lt;7%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">72 (35%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">88 (44%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">25 (12%)</td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">FPG (mg/dL) ^c</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">153</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">153</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">155</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-19</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-25</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">12</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lr

"Botrule Lrule Rrule Toprule" valign="middle">-25</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">12</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lr ule Rrule Toprule" valign="middle">-31 (-37, -26)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-36 (-42, -31)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Body Weight</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean) in kg</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">78</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">78</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">78</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">% change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.8</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-3.2</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.4</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.5 ^b(-3.1, -1.9) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.8 ^b(-3.4, -2.2) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr></tbody></table>

align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.5 ^b(-3.1, -1.9) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.8 ^b(-3.4, -2.2) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr></tbody></table> <table ID="t12297822" border="0" rules="none" width="100%"><caption>Table 5 Results at Week 24 From a Placebo-Controlled Study for JARDIANCE used in Combination with Metformin</caption><col valign="top" width="2%"/><col width="56%"/><col valign="top" width="14%"/><col valign="top" width="14%"/><col valign="top" width="14%"/><tfoot><tr><td colspan="5">^aModified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 24. At Week 24, 9.7%, 14.1%, and 24.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region.

on on study (LOCF) was used to impute missing data at Week 24. At Week 24, 9.7%, 14.1%, and 24.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) ^cFPG (mg/dL); for JARDIANCE 10 mg, n=216, for JARDIANCE 25 mg, n=213, and for placebo, n=207 </td></tr></tfoot><tbody><tr><td colspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">JARDIANCE 10 mg + Metformin N=217 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">JARDIANCE 25 mg + Metformin N=213 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">Placebo + Metformin N=207 </content></td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">HbA1c (%) ^a</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">7.9</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">7.9</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">7.9</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.7</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.8</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.1</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo + metformin (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.6 ^b(-0.7, -0.4) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.6 ^b(-0.8, -0.5) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Patients [n (%)] achieving HbA1c &lt;7%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">75 (38%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">74 (39%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">23 (13%)</td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">FPG (mg/dL) ^c</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">155</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">149</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">156</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-20</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-22</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">6</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo + metformin (adjusted m

="middle">-20</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-22</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">6</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo + metformin (adjusted m ean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-26</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-29</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Body Weight</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline mean in kg</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">82</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">82</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">80</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">% change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.5</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.9</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.5</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.0 ^b(-2.6, -1.4) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.5 ^b(-3.1, -1.9) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr></tbody></table>

align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.0 ^b(-2.6, -1.4) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.5 ^b(-3.1, -1.9) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr></tbody></table> <table ID="t174095386" border="0" width="100%"><caption>Table 6 Glycemic Parameters at 24 Weeks in a Study Comparing JARDIANCE and Metformin to the Individual Components as Initial Therapy</caption><col/><col/><col/><col/><col/><col/><col/><col/><col/><tfoot><tr><td colspan="9">^aMetformin total daily dose, administered in two equally divided doses per day. ^bp-value &#x2264;0.0062 (modified intent to treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c). ^cp-value &#x2264;0.0056 (modified intent to treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c).

e] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c). ^cp-value &#x2264;0.0056 (modified intent to treat population [observed case] MMRM model included treatment, renal function, region, visit, visit by treatment interaction, and baseline HbA1c). </td></tr></tfoot><tbody><tr><td styleCode="Toprule Botrule Rrule Lrule"> </td><td align="center" styleCode="Toprule Botrule Rrule Lrule" valign="top"><content styleCode="bold">JARDIANCE 10 mg + Metformin 1000 mg ^a N=161 </content></td><td align="center" styleCode="Toprule Botrule Rrule Lrule" valign="top"><content styleCode="bold">JARDIANCE 10 mg + Metformin 2000 mg ^a N=167 </content></td><td align="center" styleCode="Toprule Botrule Rrule Lrule" valign="top"><content styleCode="bold">JARDIANCE 25 mg + Metformin 1000 mg ^a N=165 </content></td><td align="center" styleCode="Toprule Botrule Rrule Lrule" valign="top"><content styleCode="bold">JARDIANCE 25 mg + Metformin 2000 mg ^a N=169 </content></td><td align="center" styleCode="Toprule Botrule Rrule Lrule" valign="top"><content styleCode="bold">JARDIANCE 10 mg N=169 </content></td><td align="center" styleCode="Toprule Botrule Rrule Lrule" valign="top"><content styleCode="bold">JARDIANCE 25 mg N=163 </content></td><td align="center" styleCode="Toprule Botrule Rrule Lrule" valign="top"><content styleCode="bold">Metformin 1000 mg ^a N=167 </content></td><td align="center" styleCode="Toprule Botrule Rrule Lrule" valign="top"><content styleCode="bold">Metformin 2000 mg ^a N=162 </content></td></tr><tr><td styleCode="Toprule Botrule Rrule Lrule"><content styleCode="bold">HbA1c (%)</content></td><td styleCode="Toprule Botrule Rrule Lrule"> </td><td styleCode="Toprule Botrule Rrule Lrule"> </td><td styleCode="Toprule Botrule Rrule Lrule"> </td><td styleCode="Toprule Botrule Rrule Lrule"> </td><td styleCode="Toprule Botrule Rrule Lrule"> </td><td styleCode="Toprule Botrule Rrule Lrule"> </td><td styleCode="Toprule Botrule Rrule Lrule"> </td><td styleCode="Toprule Botrule Rrule Lrule"> </td></tr><tr><td styleCode="Toprule Botrule Rrule Lrule">Baseline (mean)</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">8.7</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">8.7</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">8.8</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">8.7</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">8.6</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">8.9</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">8.7</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">8.6</td></tr><tr><td styleCode="Toprule Botrule Rrule Lrule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-2.0</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-2.1</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-1.9</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-2.1</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-1.4</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-1.4</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-1.2</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-1.8</td></tr><tr><td styleCode="Toprule Botrule Rrule Lrule">Comparison vs JARDIANCE (adjusted mean) (95% CI)</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-0.6 ^b (-0.9, -0.4) </td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-0.7 ^b (-1.0, -0.5) </td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-0.6 ^c (-0.8, -0.3) </td><td align="center" styleCode="Toprule

align="center" styleCode="Toprule Botrule Rrule Lrule">-0.6 ^b (-0.9, -0.4) </td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-0.7 ^b (-1.0, -0.5) </td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-0.6 ^c (-0.8, -0.3) </td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-0.7 ^c (-1.0, -0.5) </td><td align="center" styleCode="Toprule Botrule Rrule Lrule">--</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">--</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">--</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">--</td></tr><tr><td styleCode="Toprule Botrule Rrule Lrule">Comparison vs metformin (adjusted mean) (95% CI)</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-0.8 ^b (-1.0, -0.6) </td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-0.3 ^b (-0.6, -0.1) </td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-0.8 ^c (-1.0, -0.5) </td><td align="center" styleCode="Toprule Botrule Rrule Lrule">-0.3 ^c (-0.6, -0.1) </td><td align="center" styleCode="Toprule Botrule Rrule Lrule">--</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">--</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">--</td><td align="center" styleCode="Toprule Botrule Rrule Lrule">--</td></tr></tbody></table> <table ID="t13873522" border="0" width="100%"><caption>Table 7 Results at Week 24 from a Placebo-Controlled Study for JARDIANCE in Combination with Metformin and Sulfonylurea</caption><col valign="top" width="2.5%"/><col width="37.5%"/><col valign="top" width="20%"/><col valign="top" width="20%"/><col valign="top" width="20%"/><tfoot><tr><td colspan="5">^aModified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 24. At Week 24, 17.8%, 16.7%, and 25.3% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region.

n on study (LOCF) was used to impute missing data at Week 24. At Week 24, 17.8%, 16.7%, and 25.3% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) ^cFPG (mg/dL); for JARDIANCE 10 mg, n=225, for JARDIANCE 25 mg, n=215, for placebo, n=224 </td></tr></tfoot><tbody><tr><td colspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 10 mg + Metformin + SU N=225 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg + Metformin + SU N=216 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Placebo + Metformin + SU N=225 </content></td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">HbA1c (%) ^a</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">8.1</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">8.1</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">8.2</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.8</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.8</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.2</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.6 ^b(-0.8, -0.5) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.6 ^b(-0.7, -0.4) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Patients [n (%)] achieving HbA1c &lt;7%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">55 (26%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">65 (32%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">20 (9%)</td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">FPG (mg/dL) ^c</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">151</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">156</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">152</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-23</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-23</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">6</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Top

trule Lrule Rrule Toprule" valign="middle">-23</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">6</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Top rule" valign="middle">-29</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-29</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Body Weight</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline mean in kg</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">77</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">78</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">76</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">% change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.9</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-3.2</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-0.5</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.4 ^b(-3.0, -1.8) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.7 ^b(-3.3, -2.1) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr></tbody></table>

align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.4 ^b(-3.0, -1.8) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">-2.7 ^b(-3.3, -2.1) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle">--</td></tr></tbody></table> <table ID="t14892722" border="0" width="100%"><caption>Table 8 Results at Week 52 from an Active-Controlled Study Comparing JARDIANCE to Glimepiride as Add-On Therapy in Patients Inadequately Controlled on Metformin</caption><col width="2%"/><col width="54%"/><col width="22%"/><col width="22%"/><tfoot><tr><td colspan="4">^aModified intent to treat population. Last observation on study (LOCF) was used to impute data missing at Week 52. At Week 52, data was imputed for 15.3% and 21.9% of patients randomized to JARDIANCE 25 mg and glimepiride, respectively.

th="54%"/><col width="22%"/><col width="22%"/><tfoot><tr><td colspan="4">^aModified intent to treat population. Last observation on study (LOCF) was used to impute data missing at Week 52. At Week 52, data was imputed for 15.3% and 21.9% of patients randomized to JARDIANCE 25 mg and glimepiride, respectively. ^bNon-inferior, ANCOVA model p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and region) ^cANCOVA p-value &lt;0.0001 (Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) ^dFPG (mg/dL); for JARDIANCE 25 mg, n=764, for placebo, n=779 </td></tr></tfoot><tbody><tr><td colspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg + Metformin N=765 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Glimepiride + Metformin N=780 </content></td></tr><tr><td colspan="4" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">HbA1c (%) ^a</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">7.9</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">7.9</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.7</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.7</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from glimepiride (adjusted mean) (97.5% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.07 ^b(-0.15, 0.01) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr><tr><td colspan="4" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">FPG (mg/dL) ^d</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">150</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">150</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-19</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-9</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from glimepiride (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-11</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr><tr><td colspan="4" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Body Weight</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline mean in kg</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">82.5</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">83</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">% change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-3.9</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">2.0</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from glimepiride (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-5.9 ^c(-6.3, -5.5) </td><td align="center" sty

center" styleCode="Botrule Lrule Rrule Toprule">2.0</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from glimepiride (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-5.9 ^c(-6.3, -5.5) </td><td align="center" sty leCode="Botrule Lrule Rrule Toprule">--</td></tr></tbody></table> <table ID="t16683722" border="0" width="100%"><caption>Table 9 Results of Placebo-Controlled Study for JARDIANCE in Combination Therapy with Pioglitazone</caption><col width="2.5%"/><col width="37.5%"/><col width="20%"/><col width="20%"/><col width="20%"/><tfoot><tr><td colspan="5">^aModified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 24. At Week 24, 10.9%, 8.3%, and 20.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and background medication.

CF) was used to impute missing data at Week 24. At Week 24, 10.9%, 8.3%, and 20.6% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and background medication. Body weight and FPG: same model used as for HbA1c but additionally including baseline body weight/baseline FPG, respectively.) ^cFPG (mg/dL); for JARDIANCE 10 mg, n=163 </td></tr></tfoot><tbody><tr valign="top"><td colspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">JARDIANCE 10 mg + Pioglitazone N=165 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">JARDIANCE 25 mg + Pioglitazone N=168 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">Placebo + Pioglitazone N=165 </content></td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">HbA1c (%) ^a</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">8.1</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">8.1</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">8.2</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.6</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.7</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.1</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo + pioglitazone (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.5 ^b(-0.7, -0.3) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.6 ^b(-0.8, -0.4) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Patients [n (%)] achieving HbA1c &lt;7%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">36 (24%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">48 (30%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">12 (8%)</td></tr><tr><td colspan="5" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">FPG (mg/dL) ^c</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">152</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">152</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">152</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-17</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-22</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">7</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo + pioglitazone (adjusted mean) (97.5% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-23 ^b(-31.8, -15.2) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-28 ^b(-36.7, -20.2) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr><tr><td colspan="5" styleCode="B

usted mean) (97.5% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-23 ^b(-31.8, -15.2) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-28 ^b(-36.7, -20.2) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr><tr><td colspan="5" styleCode="B otrule Lrule Rrule Toprule"><content styleCode="bold">Body Weight</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline mean in kg</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">78</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">79</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">78</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">% change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-2.0</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-1.8</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.6</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-2.6 ^b(-3.4, -1.8) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-2.4 ^b(-3.2, -1.6) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr></tbody></table>

ce from placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-2.6 ^b(-3.4, -1.8) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-2.4 ^b(-3.2, -1.6) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr></tbody></table> <table ID="t3344222" border="0" width="100%"><caption>Table 10 Results at Week 18 and 78 for a Placebo-Controlled Study for JARDIANCE in Combination with Insulin</caption><col width="2.5%"/><col width="19.5%"/><col width="13%"/><col width="13%"/><col width="13%"/><col width="13%"/><col width="13%"/><col width="13%"/><tfoot><tr><td colspan="8">^aModified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 18 and 78. At Week 18, 21.3%, 30.3%, and 21.8% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. At Week 78, 32.5%, 38.1% and 42.4% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, and region; FPG: MMRM model includes baseline FPG, baseline HbA1c, treatment, region, visit and visit by treatment interaction. Body weight: MMRM model includes baseline body weight, baseline HbA1c, treatment, region, visit and visit by treatment interaction.

001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, and region; FPG: MMRM model includes baseline FPG, baseline HbA1c, treatment, region, visit and visit by treatment interaction. Body weight: MMRM model includes baseline body weight, baseline HbA1c, treatment, region, visit and visit by treatment interaction. ^cp-value=0.0049 ^dp-value=0.0052 ^ep-value=0.0463 </td></tr></tfoot><tbody><tr><td colspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td colspan="3" align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"><content styleCode="bold">18 weeks (no insulin adjustment) </content></td><td colspan="3" align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"><content styleCode="bold">78 weeks (adjustable insulin dose after 18 weeks) </content></td></tr><tr valign="top"><td colspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">JARDIANCE 10 mg + Insulin N=169 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">JARDIANCE 25 mg + Insulin N=155 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">Placebo + Insulin N=170 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">JARDIANCE 10 mg + Insulin N=169 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">JARDIANCE 25 mg + Insulin N=155 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="middle"><content styleCode="bold">Placebo + Insulin N=170 </content></td></tr><tr><td colspan="8" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">HbA1c (%) ^a</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">8.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">8.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">8.2</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">8.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">8.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">8.2</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.6</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.7</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.4</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.6</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.1</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean) (97.5% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.6 ^b (-0.8, -0.4) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.7 ^b (-0.9, -0.5) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.5 ^b (-0.7, -0.3) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.7 ^b (-0.9, -0.5) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Patients (%) achieving HbA1c &lt;7%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">18.0</td><td a

rule Toprule">-0.7 ^b (-0.9, -0.5) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Patients (%) achieving HbA1c &lt;7%</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">18.0</td><td a lign="center" styleCode="Botrule Lrule Rrule Toprule">19.5</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">5.5</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">12.0</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">17.5</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">6.7</td></tr><tr><td colspan="8" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">FPG (mg/dL)</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">138</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">146</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">142</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">138</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">146</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">142</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Change from baseline (adjusted mean, SE)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-17.9 (3.2) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-19.1 (3.3) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">10.4 (3.1)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-10.1 (3.2)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-15.2 (3.4)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">2.8 (3.2)</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-28.2 ^b(-37.0, -19.5) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-29.5 ^b(-38.4, -20.6) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-12.9 ^c (-21.9, 3.9) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-17.9 ^b (-27.0, -8.8) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr><tr><td colspan="8" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Body Weight</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Baseline mean in kg</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">92</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">95</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">90</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">92</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">95</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">90</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">% change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-1.8</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-1.4</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.1</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-2.4</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-2.4</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.7</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adju

align="center" styleCode="Botrule Lrule Rrule Toprule">-2.4</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-2.4</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.7</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule">Difference from placebo (adju sted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-1.7 ^d (-3.0, -0.5) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-1.3 ^e (-2.5, -0.0) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-3.0 ^b (-4.4, -1.7) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-3.0 ^b (-4.4, -1.6) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr></tbody></table>

eCode="Botrule Lrule Rrule Toprule">--</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-3.0 ^b (-4.4, -1.7) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-3.0 ^b (-4.4, -1.6) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule">--</td></tr></tbody></table> <table ID="t174556386" border="0" width="100%"><caption>Table 11 Results at Week 18 for a Placebo-Controlled Study for JARDIANCE in Combination with Insulin and with or without Metformin</caption><col/><col/><col/><col/><tfoot><tr><td colspan="4">^aModified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 18. At Week 18, 23.7%, 22.8% and 23.4% was imputed for patients randomized to JARDIANCE 10 mg, JARDIANCE 25 mg, and placebo, respectively. ^bANCOVA p-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, geographical region, and background medication). </td></tr></tfoot><tbody><tr><td styleCode="Botrule Lrule Rrule Toprule"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"><content styleCode="bold">JARDIANCE 10 mg + Insulin +/- Metformin N=186 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"><content styleCode="bold">JARDIANCE 25 mg + Insulin +/- Metformin N=189 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top"><content styleCode="bold">Placebo + Insulin +/- Metformin N=188 </content></td></tr><tr><td colspan="4" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">HbA1c (%) ^a</content></td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule"> Baseline (mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">8.4</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">8.3</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">8.3</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule"> Change from baseline (adjusted mean)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-0.9</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-1.0</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-0.5</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule"> Difference from placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-0.4 ^b(-0.6, -0.3) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-0.5 ^b(-0.7, -0.4) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td></tr></tbody></table>

)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-0.4 ^b(-0.6, -0.3) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">-0.5 ^b(-0.7, -0.4) </td><td align="center" styleCode="Botrule Lrule Rrule Toprule" valign="top">--</td></tr></tbody></table> <table ID="t20256922" border="0" width="100%"><caption>Table 12 Results at Week 24 (LOCF) of Placebo-Controlled Study for JARDIANCE in Patients with Type 2 Diabetes and Renal Impairment</caption><col width="2%"/><col width="48%"/><col width="50%"/><tfoot><tr><td colspan="3">^ap-value &lt;0.0001 (HbA1c: ANCOVA model includes baseline HbA1c, treatment, renal function, and background medication) ^beGFR 30 to less than 90 mL/min/1.73 m ²- Modified intent to treat population. Last observation on study (LOCF) was used to impute missing data at Week 24. At Week 24, 24.6% and 26.2% was imputed for patients randomized to JARDIANCE 25 mg and placebo, respectively. </td></tr></tfoot><tbody><tr valign="top"><td colspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Mild and Moderate Impairment ^b</content></td></tr><tr><td colspan="2" styleCode="Botrule Lrule Rrule Toprule"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE 25 mg</content></td></tr><tr><td colspan="3" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">HbA1c</content></td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule" valign="top">Number of patients</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">n=284</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule" valign="top">Comparison vs placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.5 ^a(-0.6, -0.4) </td></tr></tbody></table>

styleCode="Botrule Lrule Rrule Toprule">n=284</td></tr><tr><td styleCode="Botrule Lrule Toprule"> </td><td styleCode="Botrule Rrule Toprule" valign="top">Comparison vs placebo (adjusted mean) (95% CI)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">-0.5 ^a(-0.6, -0.4) </td></tr></tbody></table> <table ID="t2742012921513221263" border="0" cellpadding="4" cellspacing="0"><caption>Table 13 Treatment Effect for the Primary Composite Endpoint, and its Components ^a</caption><tfoot><tr><td colspan="4">^aTreated set (patients who had received at least one dose of study drug) ^bp&#x2212;value for superiority (2&#x2212;sided) 0.04 ^cTotal number of events </td></tr></tfoot><tbody><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top"> </td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Placebo</content><content styleCode="bold"> N=2333 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">JARDIANCE</content><content styleCode="bold"> N=4687 </content></td><td align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Hazard ratio vs placebo </content> <content styleCode="bold">(95% CI)</content></td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top">Composite of cardiovascular death, non-fatal myocardial infarction, non-fatal stroke (time to first occurrence) ^b</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">282 (12.1%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">490 (10.5%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.86 (0.74, 0.99)</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Non-fatal myocardial infarction ^c</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">121 (5.2%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">213 (4.5%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.87 (0.70, 1.09)</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Non-fatal stroke ^c</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">60 (2.6%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">150 (3.2%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">1.24 (0.92, 1.67)</td></tr><tr><td styleCode="Botrule Lrule Rrule Toprule">Cardiovascular death ^c</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">137 (5.9%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">172 (3.7%)</td><td align="center" styleCode="Botrule Lrule Rrule Toprule">0.62 (0.49, 0.77)</td></tr></tbody></table>

16 HOW SUPPLIED/STORAGE AND HANDLING JARDIANCE tablets are available in 10 mg and 25 mg strengths as follows: 10 mg tablets: pale yellow, round, biconvex and bevel-edged, film-coated tablets debossed with “S 10” on one side and the Boehringer Ingelheim company symbol on the other side. Bottles of 30 (NDC 0597-0152-30) Bottles of 90 (NDC 0597-0152-90) Cartons containing 3 blister cards of 10 tablets each (3 x 10) (NDC 0597-0152-37), institutional pack. 25 mg tablets: pale yellow, oval, biconvex film-coated tablets, debossed with “S 25” on one side and the Boehringer Ingelheim company symbol on the other side. Bottles of 30 (NDC 0597-0153-30) Bottles of 90 (NDC 0597-0153-90) Cartons containing 3 blister cards of 10 tablets each (3 x 10) (NDC 0597-0153-37), institutional pack. Dispense in a well-closed container as defined in the USP. Storage Store at 25°C (77°F); excursions permitted to 15°-30°C (59°-86°F) [see USP Controlled Room Temperature].

17 PATIENT COUNSELING INFORMATION Advise the patient to read the FDA-approved patient labeling (Patient Information). Instructions Instruct patients to read the Patient Information before starting JARDIANCE therapy and to reread it each time the prescription is renewed. Instruct patients to inform their doctor or pharmacist if they develop any unusual symptom, or if any known symptom persists or worsens. Inform patients of the potential risks and benefits of JARDIANCE and of alternative modes of therapy. Also inform patients about the importance of adherence to dietary instructions, regular physical activity, periodic blood glucose monitoring and HbA1c testing, recognition and management of hypoglycemia and hyperglycemia, and assessment for diabetes complications. Advise patients to seek medical advice promptly during periods of stress such as fever, trauma, infection, or surgery, as medication requirements may change. Instruct patients to take JARDIANCE only as prescribed. If a dose is missed, it should be taken as soon as the patient remembers. Advise patients not to double their next dose. Inform patients that the most common adverse reactions associated with the use of JARDIANCE are urinary tract infections and mycotic genital infections. Advise pregnant women, and females of reproductive potential of the potential risk to a fetus with treatment with JARDIANCE [see Use in Specific Populations ( 8.1 )] . Instruct females of reproductive potential to report pregnancies to their physicians as soon as possible. Advise women that breastfeeding is not recommended during treatment with JARDIANCE [see Use in Specific Populations ( 8.2 )]. Hypotension Inform patients that hypotension may occur with JARDIANCE and advise them to contact their healthcare provider if they experience such symptoms [see Warnings and Precautions ( 5.1 )] . Inform patients that dehydration may increase the risk for hypotension, and to have adequate fluid intake. Ketoacidosis Inform patients that ketoacidosis is a serious life-threatening condition. Cases of ketoacidosis have been reported during use of JARDIANCE. Instruct patients to check ketones (when possible) if symptoms consistent with ketoacidosis occur even if blood glucose is not elevated. If symptoms of ketoacidosis (including nausea, vomiting, abdominal pain, tiredness, and labored breathing) occur, instruct patients to discontinue JARDIANCE and seek medical advice immediately [see Warnings and Precautions ( 5.2 )] . Acute Kidney Injury Inform patients that acute kidney injury has been reported during use of JARDIANCE. Advise patients to seek medical advice immediately if they have reduced oral intake (such as due to acute illness or fasting) or increased fluid losses (such as due to vomiting, diarrhea, or excessive heat exposure), as it may be appropriate to temporarily discontinue JARDIANCE use in those settings [see Warnings and Precautions ( 5.3 )] . Serious Urinary Tract Infections Inform patients of the potential for urinary tract infections, which may be serious. Provide them with information on the symptoms of urinary tract infections. Advise them to seek medical advice if such symptoms occur [see Warnings and Precautions ( 5.4 ) ] . Genital Mycotic Infections in Females (e.g., Vulvovaginitis) Inform female patients that vaginal yeast infections may occur and provide them with information on the signs and symptoms of vaginal yeast infections.

ctions. Advise them to seek medical advice if such symptoms occur [see Warnings and Precautions ( 5.4 ) ] . Genital Mycotic Infections in Females (e.g., Vulvovaginitis) Inform female patients that vaginal yeast infections may occur and provide them with information on the signs and symptoms of vaginal yeast infections. Advise them of treatment options and when to seek medical advice [see Warnings and Precautions ( 5.6 )] . Genital Mycotic Infections in Males (e.g., Balanitis or Balanoposthitis) Inform male patients that yeast infection of penis (e.g., balanitis or balanoposthitis) may occur, especially in uncircumcised males and patients with chronic and recurrent infections. Provide them with information on the signs and symptoms of balanitis and balanoposthitis (rash or redness of the glans or foreskin of the penis). Advise them of treatment options and when to seek medical advice [see Warnings and Precautions ( 5.6 )] . Hypersensitivity Reactions Inform patients that serious hypersensitivity reactions, such as urticaria and angioedema, have been reported with JARDIANCE. Advise patients to report immediately any skin reaction or angioedema, and to discontinue drug until they have consulted prescribing physician [see Warnings and Precautions ( 5.7 )] . Laboratory Tests Inform patients that renal function should be assessed prior to initiation of JARDIANCE and monitored periodically thereafter. Inform patients that elevated glucose in urinalysis is expected when taking JARDIANCE. Inform patients that response to all diabetic therapies should be monitored by periodic measurements of blood glucose and HbA1c levels, with a goal of decreasing these levels toward the normal range. Hemoglobin A1c monitoring is especially useful for evaluating long-term glycemic control.

Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877 USA Marketed by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877 USA and Eli Lilly and Company Indianapolis, IN 46285 USA Licensed from: Boehringer Ingelheim International GmbH, Ingelheim, Germany Boehringer Ingelheim Pharmaceuticals, Inc. either owns or uses the Jardiance ® and EMPA-REG OUTCOME ® trademarks under license. The other trademarks referenced are owned by third parties not affiliated with Boehringer Ingelheim Pharmaceuticals, Inc. Copyright © 2017 Boehringer Ingelheim International GmbH ALL RIGHTS RESERVED IT5728RL112017 REPACKAGING INFORMATION Please reference the HOW SUPPLIED section listed above for a description of individual drug products listed below. This drug product has been received by Aphena Pharma Solutions - Tennessee, LLC in a manufacturer or distributor packaged configuration and repackaged in full compliance with all applicable cGMP regulations. The package configurations available from Aphena are listed below: 25mg NDC 71610-177-15, Bottles of 15 Tablets NDC 71610-177-45, Bottles of 45 Tablets NDC 71610-177-81, Bottles of 1080 Tablets NDC 71610-177-42, Bottles of 1800 Tablets NDC 71610-177-99, Bottles of 5040 Tablets NDC 71610-177-09, Bottles of 9000 Tablets Store between 20°-25°C (68°-77°F). See USP Controlled Room Temperature. Dispense in a tight light-resistant container as defined by USP. Keep this and all drugs out of the reach of children. Repackaged by: Cookeville, TN 38506 20251027AMH Aphena

This Patient Information has been approved by the U.S. Food and Drug Administration. Revised: December 2017 PATIENT INFORMATION JARDIANCE ® (jar DEE ans) (empagliflozin) Tablets What is the most important information I should know about JARDIANCE? JARDIANCE can cause serious side effects, including: Dehydration. JARDIANCE can cause some people to have dehydration (the loss of body water and salt). Dehydration may cause you to feel dizzy, faint, light-headed, or weak, especially when you stand up (orthostatic hypotension). You may be at higher risk of dehydration if you: have low blood pressure take medicines to lower your blood pressure, including diuretics (water pills) are on low sodium (salt) diet have kidney problems are 65 years of age or older Vaginal yeast infection. Women who take JARDIANCE may get vaginal yeast infections. Symptoms of a vaginal yeast infection include: vaginal odor white or yellowish vaginal discharge (discharge may be lumpy or look like cottage cheese) vaginal itching Yeast infection of the penis (balanitis or balanoposthitis). Men who take JARDIANCE may get a yeast infection of the skin around the penis. Certain men who are not circumcised may have swelling of the penis that makes it difficult to pull back the skin around the tip of the penis. Other symptoms of yeast infection of the penis include: redness, itching, or swelling of the penis rash of the penis foul smelling discharge from the penis pain in the skin around penis Talk to your doctor about what to do if you get symptoms of a yeast infection of the vagina or penis. Your doctor may suggest you use an over-the-counter antifungal medicine. Talk to your doctor right away if you use an over-the-counter antifungal medication and your symptoms do not go away. What is JARDIANCE? JARDIANCE is a prescription medicine used: along with diet and exercise to lower blood sugar in adults with type 2 diabetes. to reduce the risk of cardiovascular death in adults with type 2 diabetes who have known cardiovascular disease. JARDIANCE is not for people with type 1 diabetes. JARDIANCE is not for people with diabetic ketoacidosis (increased ketones in the blood or urine). It is not known if JARDIANCE is safe and effective in children under 18 years of age. Who should not take JARDIANCE? Do not take JARDIANCE if you: are allergic to empagliflozin or any of the ingredients in JARDIANCE. See the end of this leaflet for a list of ingredients in JARDIANCE. have severe kidney problems or are on dialysis What should I tell my doctor before using JARDIANCE? Before you take JARDIANCE, tell your doctor if you: have kidney problems have liver problems have a history of urinary tract infections or problems with urination are going to have surgery are eating less due to illness, surgery, or a change in your diet have or have had problems with your pancreas, including pancreatitis or surgery on your pancreas drink alcohol very often, or drink a lot of alcohol in the short term (“binge” drinking) have any other medical conditions are pregnant or plan to become pregnant. JARDIANCE may harm your unborn baby. If you become pregnant while taking JARDIANCE, tell your doctor as soon as possible. Talk with your doctor about the best way to control your blood sugar while you are pregnant. are breastfeeding or plan to breastfeed. JARDIANCE may pass into your breast milk and may harm your baby. Talk with your doctor about the best way to feed your baby if you are taking JARDIANCE.

your doctor as soon as possible. Talk with your doctor about the best way to control your blood sugar while you are pregnant. are breastfeeding or plan to breastfeed. JARDIANCE may pass into your breast milk and may harm your baby. Talk with your doctor about the best way to feed your baby if you are taking JARDIANCE. Do not breastfeed while taking JARDIANCE. Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. JARDIANCE may affect the way other medicines work, and other medicines may affect how JARDIANCE works. Especially tell your doctor if you take: diuretics (water pills) insulin or other medicines that can lower your blood sugar Ask your doctor or pharmacist for a list of these medicines if you are not sure if your medicine is listed above. How should I take JARDIANCE? Take JARDIANCE exactly as your doctor tells you to take it. Take JARDIANCE by mouth 1 time in the morning each day, with or without food. Your doctor may change your dose if needed. If you miss a dose, take it as soon as you remember. If you do not remember until it is time for your next dose, skip the missed dose and go back to your regular schedule. Do not take two doses of JARDIANCE at the same time. Talk with your doctor if you have questions about a missed dose. Your doctor may tell you to take JARDIANCE along with other diabetes medicines. Low blood sugar can happen more often when JARDIANCE is taken with certain other diabetes medicines. See “What are the possible side effects of JARDIANCE?” If you take too much JARDIANCE, call your doctor or go to the nearest hospital emergency room right away. When your body is under some types of stress, such as fever, trauma (such as a car accident), infection, or surgery, the amount of diabetes medicine that you need may change. Tell your doctor right away if you have any of these conditions and follow your doctor’s instructions. Check your blood sugar as your doctor tells you to. Stay on your prescribed diet and exercise program while taking JARDIANCE. Talk to your doctor about how to prevent, recognize and manage low blood sugar (hypoglycemia), high blood sugar (hyperglycemia), and complications of diabetes. Your doctor will check your diabetes with regular blood tests, including your blood sugar levels and your hemoglobin HbA1c. When taking JARDIANCE, you may have sugar in your urine, which will show up on a urine test. What are the possible side effects of JARDIANCE? JARDIANCE may cause serious side effects, including: See “ What is the most important information I should know about JARDIANCE? ” Ketoacidosis (increased ketones in your blood or urine). Ketoacidosis has happened in people who have type 1 diabetes or type 2 diabetes, during treatment with JARDIANCE. Ketoacidosis is a serious condition, which may need to be treated in a hospital. Ketoacidosis may lead to death. Ketoacidosis can happen with JARDIANCE even if your blood sugar is less than 250 mg/dL. Stop taking JARDIANCE and call your doctor right away if you get any of the following symptoms : nausea vomiting stomach-area (abdominal) pain tiredness trouble breathing If you get any of these symptoms during treatment with JARDIANCE, if possible, check for ketones in your urine, even if your blood sugar is less than 250 mg/dL. Serious urinary tract infections. Serious urinary tract infections that may lead to hospitalization have happened in people who are taking JARDIANCE. Tell your doctor if you have any signs or symptoms of a urinary tract infection such as a burning feeling when passing urine, a need to urinate often, the need to urinate right away, pain in the lower part of your stomach (pelvis), or blood in the urine.

hospitalization have happened in people who are taking JARDIANCE. Tell your doctor if you have any signs or symptoms of a urinary tract infection such as a burning feeling when passing urine, a need to urinate often, the need to urinate right away, pain in the lower part of your stomach (pelvis), or blood in the urine. Sometimes people also may have a fever, back pain, nausea or vomiting. Low blood sugar (hypoglycemia). If you take JARDIANCE with another medicine that can cause low blood sugar, such as a sulfonylurea or insulin, your risk of getting low blood sugar is higher. The dose of your sulfonylurea medicine or insulin may need to be lowered while you take JARDIANCE. Signs and symptoms of low blood sugar may include: headache drowsiness weakness irritability hunger fast heartbeat confusion shaking or feeling jittery dizziness sweating Kidney problems. Sudden kidney injury has happened to people taking JARDIANCE. Talk to your doctor right away if you: reduce the amount of food or liquid you drink for example, if you are sick or cannot eat or start to lose liquids from your body for example, from vomiting, diarrhea or being in the sun too long Allergic (hypersensitivity) reactions. Serious allergic reactions have happened in people who are taking JARDIANCE. Symptoms may include swelling of your face, lips, throat and other areas of your skin difficulty with swallowing or breathing. raised, red areas on your skin (hives) If you have any of these symptoms, stop taking JARDIANCE and call your doctor right away or go to the nearest hospital emergency room. Increased fats in your blood (cholesterol) These are not all the possible side effects of JARDIANCE. For more information, ask your doctor or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. How should I store JARDIANCE? Store JARDIANCE at room temperature 68°F to 77°F (20°C to 25°C). General information about the safe and effective use of JARDIANCE. Medicines are sometimes prescribed for purposes other than those listed in Patient Information. Do not use JARDIANCE for a condition for which it is not prescribed. Do not give JARDIANCE to other people, even if they have the same symptoms you have. It may harm them. This Patient Information summarizes the most important information about JARDIANCE. If you would like more information, talk with your doctor. You can ask your pharmacist or doctor for information about JARDIANCE that is written for health professionals. For more information about JARDIANCE, go to www.jardiance.com , scan the code below, or call Boehringer Ingelheim Pharmaceuticals, Inc. at 1-800-542-6257 or (TTY) 1-800-459-9906. What are the ingredients in JARDIANCE? Active Ingredient: empagliflozin Inactive Ingredients: lactose monohydrate, microcrystalline cellulose, hydroxypropyl cellulose, croscarmellose sodium, colloidal silicon dioxide and magnesium stearate. In addition, the film coating contains the following inactive ingredients: hypromellose, titanium dioxide, talc, polyethylene glycol, and yellow ferric oxide. Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc.; Ridgefield, CT 06877 USA Marketed by: Boehringer Ingelheim Pharmaceuticals, Inc.; Ridgefield, CT 06877 USA and Eli Lilly and Company, Indianapolis, IN 46285 USA Licensed from: Boehringer Ingelheim International GmbH, Ingelheim, Germany Boehringer Ingelheim Pharmaceuticals, Inc. either owns or uses the Jardiance ® and EMPA-REG OUTCOME ® trademarks under license. The other trademarks referenced are owned by third parties not affiliated with Boehringer Ingelheim Pharmaceuticals, Inc. Copyright © 2017 Boehringer Ingelheim International GmbH ALL RIGHTS RESERVED IT5728RL112017 qr-code

<table ID="t304866386" border="0" width="100%"><col/><col/><col/><col/><col/><col/><tfoot><tr><td colspan="4" align="left">This Patient Information has been approved by the U.S. Food and Drug Administration.</td><td colspan="2" align="right">Revised: December 2017</td></tr></tfoot><tbody><tr><td colspan="6" align="center" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">PATIENT INFORMATION JARDIANCE ^&#xAE;(jar DEE ans) (empagliflozin) Tablets </content></td></tr><tr><td colspan="6" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">What is the most important information I should know about JARDIANCE?</content> JARDIANCE can cause serious side effects, including: <list listType="unordered" styleCode="Disc"><item><content styleCode="bold">Dehydration.</content>JARDIANCE can cause some people to have dehydration (the loss of body water and salt). Dehydration may cause you to feel dizzy, faint, light-headed, or weak, especially when you stand up (orthostatic hypotension). You may be at higher risk of dehydration if you: <list listType="unordered" styleCode="Circle"><item>have low blood pressure</item><item>take medicines to lower your blood pressure, including diuretics (water pills)</item><item>are on low sodium (salt) diet</item><item>have kidney problems</item><item>are 65 years of age or older</item></list></item><item><content styleCode="bold">Vaginal yeast infection.</content>Women who take JARDIANCE may get vaginal yeast infections. Symptoms of a vaginal yeast infection include: <list listType="unordered" styleCode="Circle"><item>vaginal odor</item><item>white or yellowish vaginal discharge (discharge may be lumpy or look like cottage cheese)</item><item>vaginal itching</item></list></item><item><content styleCode="bold">Yeast infection of the penis (balanitis or balanoposthitis).</content>Men who take JARDIANCE may get a yeast infection of the skin around the penis. Certain men who are not circumcised may have swelling of the penis that makes it difficult to pull back the skin around the tip of the penis. Other symptoms of yeast infection of the penis include: <list listType="unordered" styleCode="Circle"><item>redness, itching, or swelling of the penis</item><item>rash of the penis</item><item>foul smelling discharge from the penis</item><item>pain in the skin around penis</item></list></item></list>Talk to your doctor about what to do if you get symptoms of a yeast infection of the vagina or penis. Your doctor may suggest you use an over-the-counter antifungal medicine. Talk to your doctor right away if you use an over-the-counter antifungal medication and your symptoms do not go away.

</item></list></item></list>Talk to your doctor about what to do if you get symptoms of a yeast infection of the vagina or penis. Your doctor may suggest you use an over-the-counter antifungal medicine. Talk to your doctor right away if you use an over-the-counter antifungal medication and your symptoms do not go away. </td></tr><tr><td colspan="6" styleCode="Botrule Lrule Rrule Toprule"><list listType="unordered" styleCode="Disc"><caption>What is JARDIANCE?</caption><item>JARDIANCE is a prescription medicine used: <list listType="unordered" styleCode="Circle"><item>along with diet and exercise to lower blood sugar in adults with type 2 diabetes.</item><item>to reduce the risk of cardiovascular death in adults with type 2 diabetes who have known cardiovascular disease.</item></list></item><item>JARDIANCE is not for people with type 1 diabetes.</item><item>JARDIANCE is not for people with diabetic ketoacidosis (increased ketones in the blood or urine).</item><item>It is not known if JARDIANCE is safe and effective in children under 18 years of age.</item></list></td></tr><tr><td colspan="6" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">Who should not take JARDIANCE?</content><list listType="unordered" styleCode="Disc"><caption>Do not take JARDIANCE if you:</caption><item>are allergic to empagliflozin or any of the ingredients in JARDIANCE. See the end of this leaflet for a list of ingredients in JARDIANCE.</item><item>have severe kidney problems or are on dialysis</item></list></td></tr><tr><td colspan="6" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">What should I tell my doctor before using JARDIANCE?</content><list listType="unordered" styleCode="Disc"><caption>Before you take JARDIANCE, tell your doctor if you:</caption><item>have kidney problems</item><item>have liver problems</item><item>have a history of urinary tract infections or problems with urination</item><item>are going to have surgery</item><item>are eating less due to illness, surgery, or a change in your diet</item><item>have or have had problems with your pancreas, including pancreatitis or surgery on your pancreas</item><item>drink alcohol very often, or drink a lot of alcohol in the short term (&#x201C;binge&#x201D; drinking)</item><item>have any other medical conditions</item><item>are pregnant or plan to become pregnant. JARDIANCE may harm your unborn baby. If you become pregnant while taking JARDIANCE, tell your doctor as soon as possible. Talk with your doctor about the best way to control your blood sugar while you are pregnant.</item><item>are breastfeeding or plan to breastfeed. JARDIANCE may pass into your breast milk and may harm your baby. Talk with your doctor about the best way to feed your baby if you are taking JARDIANCE. Do not breastfeed while taking JARDIANCE.</item></list><content styleCode="bold">Tell your doctor about all the medicines you take,</content>including prescription and over-the-counter medicines, vitamins, and herbal supplements. JARDIANCE may affect the way other medicines work, and other medicines may affect how JARDIANCE works. <list listType="unordered" styleCode="Disc"><caption>Especially tell your doctor if you take:</caption><item>diuretics (water pills)</item><item>insulin or other medicines that can lower your blood sugar</item></list>Ask your doctor or pharmacist for a list of these medicines if you are not sure if your medicine is listed above.

Type="unordered" styleCode="Disc"><caption>Especially tell your doctor if you take:</caption><item>diuretics (water pills)</item><item>insulin or other medicines that can lower your blood sugar</item></list>Ask your doctor or pharmacist for a list of these medicines if you are not sure if your medicine is listed above. </td></tr><tr><td colspan="6" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">How should I take JARDIANCE?</content> <list listType="unordered" styleCode="Disc"><item>Take JARDIANCE exactly as your doctor tells you to take it.</item><item>Take JARDIANCE by mouth 1 time in the morning each day, with or without food.</item><item>Your doctor may change your dose if needed.</item><item>If you miss a dose, take it as soon as you remember. If you do not remember until it is time for your next dose, skip the missed dose and go back to your regular schedule. Do not take two doses of JARDIANCE at the same time. Talk with your doctor if you have questions about a missed dose.</item><item>Your doctor may tell you to take JARDIANCE along with other diabetes medicines. Low blood sugar can happen more often when JARDIANCE is taken with certain other diabetes medicines. See <content styleCode="bold">&#x201C;What are the possible side effects of JARDIANCE?&#x201D;</content></item><item>If you take too much JARDIANCE, call your doctor or go to the nearest hospital emergency room right away.</item><item>When your body is under some types of stress, such as fever, trauma (such as a car accident), infection, or surgery, the amount of diabetes medicine that you need may change. Tell your doctor right away if you have any of these conditions and follow your doctor&#x2019;s instructions.</item><item>Check your blood sugar as your doctor tells you to.</item><item>Stay on your prescribed diet and exercise program while taking JARDIANCE.</item><item>Talk to your doctor about how to prevent, recognize and manage low blood sugar (hypoglycemia), high blood sugar (hyperglycemia), and complications of diabetes.</item><item>Your doctor will check your diabetes with regular blood tests, including your blood sugar levels and your hemoglobin HbA1c.</item><item>When taking JARDIANCE, you may have sugar in your urine, which will show up on a urine test.</item></list></td></tr><tr><td colspan="6" styleCode="Lrule Rrule Toprule"><content styleCode="bold">What are the possible side effects of JARDIANCE?</content><list listType="unordered" styleCode="Disc"><caption>JARDIANCE may cause serious side effects, including:</caption><item>See &#x201C; <content styleCode="bold">What is the most important information I should know about JARDIANCE?</content>&#x201D; </item><item><content styleCode="bold">Ketoacidosis (increased ketones in your blood or urine).</content>Ketoacidosis has happened in people who have <content styleCode="bold">type 1 diabetes or type 2 diabetes,</content>during treatment with JARDIANCE. Ketoacidosis is a serious condition, which may need to be treated in a hospital. Ketoacidosis may lead to death.

dosis (increased ketones in your blood or urine).</content>Ketoacidosis has happened in people who have <content styleCode="bold">type 1 diabetes or type 2 diabetes,</content>during treatment with JARDIANCE. Ketoacidosis is a serious condition, which may need to be treated in a hospital. Ketoacidosis may lead to death. <content styleCode="bold">Ketoacidosis can happen with JARDIANCE even if your blood sugar is less than 250 mg/dL.</content><content styleCode="bold">Stop taking JARDIANCE and call your doctor right away if you get any of the following symptoms</content>: </item></list></td></tr><tr><td styleCode="Lrule"> </td><td valign="top"><list listType="unordered" styleCode="Circle"><item>nausea</item><item>vomiting</item><item>stomach-area (abdominal) pain</item></list></td><td valign="top"><list listType="unordered" styleCode="Circle"><item>tiredness</item><item>trouble breathing</item></list></td><td> </td><td> </td><td styleCode="Rrule"> </td></tr><tr><td colspan="6" styleCode="Lrule Rrule"> If you get any of these symptoms during treatment with JARDIANCE, if possible, check for ketones in your urine, even if your blood sugar is less than 250 mg/dL. <list listType="unordered" styleCode="Disc"><item><content styleCode="bold">Serious urinary tract infections.</content>Serious urinary tract infections that may lead to hospitalization have happened in people who are taking JARDIANCE. Tell your doctor if you have any signs or symptoms of a urinary tract infection such as a burning feeling when passing urine, a need to urinate often, the need to urinate right away, pain in the lower part of your stomach (pelvis), or blood in the urine. Sometimes people also may have a fever, back pain, nausea or vomiting. </item><item><content styleCode="bold">Low blood sugar (hypoglycemia).</content>If you take JARDIANCE with another medicine that can cause low blood sugar, such as a sulfonylurea or insulin, your risk of getting low blood sugar is higher. The dose of your sulfonylurea medicine or insulin may need to be lowered while you take JARDIANCE. Signs and symptoms of low blood sugar may include: </item></list></td></tr><tr valign="top"><td styleCode="Lrule" valign="top"> </td><td valign="top"><list listType="unordered" styleCode="Circle"><item>headache</item><item>drowsiness</item><item>weakness</item></list></td><td valign="top"><list listType="unordered" styleCode="Circle"><item>irritability</item><item>hunger</item><item>fast heartbeat</item></list></td><td valign="top"><list listType="unordered" styleCode="Circle"><item>confusion</item><item>shaking or feeling jittery</item></list></td><td valign="top"><list listType="unordered" styleCode="Circle"><item>dizziness</item><item>sweating</item></list></td><td styleCode="Rrule" valign="top"> </td></tr><tr><td colspan="6" styleCode="Botrule Lrule Rrule"><list listType="unordered" styleCode="Disc"><item><content styleCode="bold">Kidney problems.</content> Sudden kidney injury has happened to people taking JARDIANCE. Talk to your doctor right away if you: <list listType="unordered" styleCode="Circle"><item>reduce the amount of food or liquid you drink for example, if you are sick or cannot eat or</item><item>start to lose liquids from your body for example, from vomiting, diarrhea or being in the sun too long</item></list></item><item><content styleCode="bold">Allergic (hypersensitivity) reactions.</content>Serious allergic reactions have happened in people who are taking JARDIANCE.

ou are sick or cannot eat or</item><item>start to lose liquids from your body for example, from vomiting, diarrhea or being in the sun too long</item></list></item><item><content styleCode="bold">Allergic (hypersensitivity) reactions.</content>Serious allergic reactions have happened in people who are taking JARDIANCE. Symptoms may include <list listType="unordered" styleCode="Circle"><item>swelling of your face, lips, throat and other areas of your skin</item><item>difficulty with swallowing or breathing.</item><item>raised, red areas on your skin (hives)</item></list> If you have any of these symptoms, stop taking JARDIANCE and call your doctor right away or go to the nearest hospital emergency room. </item><item><content styleCode="bold">Increased fats in your blood (cholesterol)</content></item></list>These are not all the possible side effects of JARDIANCE. For more information, ask your doctor or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. </td></tr><tr><td colspan="6" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">How should I store JARDIANCE?</content> Store JARDIANCE at room temperature 68&#xB0;F to 77&#xB0;F (20&#xB0;C to 25&#xB0;C). </td></tr><tr><td colspan="6" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">General information about the safe and effective use of JARDIANCE.</content> Medicines are sometimes prescribed for purposes other than those listed in Patient Information. Do not use JARDIANCE for a condition for which it is not prescribed. Do not give JARDIANCE to other people, even if they have the same symptoms you have. It may harm them. This Patient Information summarizes the most important information about JARDIANCE. If you would like more information, talk with your doctor. You can ask your pharmacist or doctor for information about JARDIANCE that is written for health professionals. For more information about JARDIANCE, go to <content styleCode="underline">www.jardiance.com</content>, scan the code below, or call Boehringer Ingelheim Pharmaceuticals, Inc. at 1-800-542-6257 or (TTY) 1-800-459-9906. <renderMultiMedia referencedObject="g1741842171458269799"/></td></tr><tr><td colspan="6" styleCode="Botrule Lrule Rrule Toprule"><content styleCode="bold">What are the ingredients in JARDIANCE?</content> <content styleCode="bold">Active Ingredient:</content>empagliflozin <content styleCode="bold">Inactive Ingredients:</content>lactose monohydrate, microcrystalline cellulose, hydroxypropyl cellulose, croscarmellose sodium, colloidal silicon dioxide and magnesium stearate. In addition, the film coating contains the following inactive ingredients: hypromellose, titanium dioxide, talc, polyethylene glycol, and yellow ferric oxide. </td></tr><tr><td colspan="6" styleCode="Botrule Lrule Rrule Toprule">Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc.; Ridgefield, CT 06877 USA Marketed by: Boehringer Ingelheim Pharmaceuticals, Inc.; Ridgefield, CT 06877 USA and Eli Lilly and Company, Indianapolis, IN 46285 USA Licensed from: Boehringer Ingelheim International GmbH, Ingelheim, Germany Boehringer Ingelheim Pharmaceuticals, Inc. either owns or uses the Jardiance ^&#xAE;and EMPA-REG OUTCOME ^&#xAE;trademarks under license. The other trademarks referenced are owned by third parties not affiliated with Boehringer Ingelheim Pharmaceuticals, Inc. Copyright &#xA9; 2017 Boehringer Ingelheim International GmbH ALL RIGHTS RESERVED IT5728RL112017 </td></tr></tbody></table>