Classes
DEA Class; Rx
Common Brand Names; Synjardy, Synjardy XR
- Antidiabetics, Biguanides;
- Antidiabetics, SGLT2 Inhibitors
Description
Oral combination of metformin with a sodium-glucose co-transporter 2 (SGLT2) inhibitor
Used in adults with type 2 diabetes mellitus
Contraindicated in severe renal impairment
Indications
Indicated for the treatment of type 2 diabetes mellitus in combination with diet and exercise when treatment with both empagliflozin and metformin is appropriate.
Contraindications
Moderate-to-severe renal disease (eGFR <45 mL/min/1.73 m2), end-stage renal disease, or dialysis
Acute or chronic metabolic acidosis, including diabetic ketoacidosis (treat ketoacidosis with insulin)
History of serious hypersensitivity reaction to empagliflozin or metformin
Adverse Effects
- Urinary tract infection (7.6-9.3%)
- Decreased vitamin B12 levels (7%)
- Increased LDL-C (4.6-6.5%)
- Female genital mycotic infections (5.4-6.4%)
- Dyslipidemia (2.9-3.9%)
- Increased urination (3.2-3.4%)
- Male genital mycotic infections (1.6-3.1%)
- Nausea (1.1-2.3%)
- Hypoglycemia, with monotherapy (1.4-1.8%)
- <1%
- Volume depletion
- Impaired renal function
- Ketoacidosis
- Urosepsis and pyelonephritis
- Angioedema
- Skin reactions (e.g., rash, urticaria)
- Cholestatic, hepatocellular, and mixed hepatocellular liver injury
- Acute kidney injury
- Constipation
- Necrotizing fasciitis of the perineum (Fournier’s gangrene)
Warnings
Lactic acidosis is a metabolic complication that can occur due to metformin accumulation during treatment and is fatal in ~50% of cases (see Black Box Warnings)
Serious hypersensitivity reactions, (eg, angioedema) in patients receiving treatment reported postmarketing; discontinue therapy and treat promptly if it occurs per standard of care
Necrotizing fasciitis of the perineum (Fournier gangrene) reported with SGLT2 inhibitors; signs and symptoms include tenderness, redness, or swelling of the genitals or the area from the genitals back to the rectum, and have a fever above 100.4ºF or a general feeling of being unwell; if suspected, discontinue SGLT2 inhibitor and start treatment immediately with broad-spectrum antibiotics and surgical debridement if necessary
Empagliflozin causes intravascular volume contraction; symptomatic hypotension may occur after initiating, particularly in patients with renal impairment, elderly patients, patients with low systolic blood pressure, or patients taking diuretics; before initiating therapy, 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
Withholding of food and fluids during surgical or other procedures may increase risk for volume depletion, hypotension and renal impairment; therapy should be temporarily discontinued while patients have restricted food and fluid intake
Cardiovascular collapse (shock), acute myocardial infarction, sepsis, and other conditions associated with hypoxemia have been associated with lactic acidosis and may also cause prerenal azotemia; when such events occur, discontinue therapy
Administration of intravascular iodinated contrast agents in metformintreated patients has led to an acute decrease in renal function and occurrence of lactic acidosis; stop treatment at the time of, or prior to, an iodinated contrast imaging procedure in patients with an eGFR between <60 mL/min/1.73 m2; in patients with a history of hepatic impairment, alcoholism, or heart failure; or in patients who will be administered intra-arterial iodinated contrast; re-evaluate eGFR 48 hours after imaging procedure, and restart therapy if renal function is stable
Pregnancy and Lactation
Not recommended during second and third trimester of pregnancy based on animal data
Limited available data with use in pregnant women is not sufficient to determine a drug-associated risk for major birth defects and miscarriages
Metformin may result in ovulation in some anovulatory women; discuss the potential for unintended pregnancy with premenopausal women
There is no information regarding presence in human milk, the effects on breastfed infant or on milk production
Maximum Dosage
Empagliflozin 25 mg/day PO and metformin 2000 mg/day PO.
Empagliflozin 25 mg/day PO and metformin 2000 mg/day PO.
Safety and efficacy have not been established.
Safety and efficacy have not been established.
Safety and efficacy have not been established.
Safety and efficacy have not been established.
How supplied
Empagliflozin/metformin Hydrochloride
tablet, immediate-release
- 5mg/500mg
- 5mg/1000mg
- 12.5mg/500mg
- 12.5mg/1000mg
tablet, extended-release
- 5mg/1000mg
- 10mg/1000mg
- 12.5mg/1000mg
- 25mg/1000mg