Classes
DEA Class; Rx
Common Brand Names; Segluromet
- 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 due to reduced ertugliflozin efficacy and increased risk of metformin-related lactic acidosis
Indications
Indicated as adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus who are not adequately controlled on a regimen containing ertugliflozin or metformin, or in patients who are already treated with both ertugliflozin and metformin
Contraindications
Hypersensitivity to drug or excipients; reactions such as angioedema or anaphylaxis have occurred
Severe renal impairment (eGFR <30 mL/min/1.73 m2), end-stage renal disease, or dialysis
Acute or chronic metabolic acidosis, including diabetic ketoacidosis, with or without coma
Adverse Effects
Female genital mycotic infections (9.1-12.2%)
(Ertugliflozin)
Volume depletion adverse effects (1.9-4.4%)
Male genital mycotic infections (3.7-4.2%)
Urinary tract infections (4-4.1%)
Headache (2.9-3.5%)
Vaginal pruritus (2.4-2.8%)
Increased urination (2.4-2.7%)
Nasopharyngitis (2-2.5%)
Back pain (1.7-2.5%)
Renal adverse effects (1.3-2.5%)
Weight decreased (1.2-2.4%)
Thirst (1.4-2.7%)
(Metformin)
Initiating drug
- Diarrhea
- Nausea
- Vomiting
- Flatulence
- Abdominal discomfort
- Indigestion
- Asthenia
- Headache
Long-term use
- Decreased vitamin B-12 absorption, which may very rarely result in significant deficiency (eg, megaloblastic anemia)
Warnings
Cases of metformin-associated lactic acidosis reported, including fatalities (see Black Box Warnings and Contraindications)
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 100.4 F 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
Before initiating treatment in patients with one or more of risk factors, assess volume status and renal function; causes intravascular volume contraction; symptomatic hypotension may occur after initiating, particularly in patients with renal impairment, with low systolic blood pressure, on diuretics, or who are elderly
Evaluate patients for signs and symptoms of urinary tract infections and treat promptly, if indicated; serious urinary tract infections, including urosepsis and pyelonephritis, requiring hospitalization reported in patients receiving SGLT2 inhibitors
Genital mycotic infections may occur; patients with history of genital mycotic infections and uncircumcised males are more susceptible
Dose-related increases in LDL-C reported
No conclusive evidence of macrovascular risk reduction with empagliflozin or any other antidiabetic agent
Pregnancy and Lactation
Ertugliflozin
- Based on animal data showing adverse renal effects, not recommended during the second and third trimesters of pregnancy
Metformin
- Published data from postmarketing studies have not reported a clear association with metformin and major birth defects, miscarriage, or adverse maternal or fetal outcomes when metformin was used during pregnancy
Lactation
Not recommended while breastfeeding
Maximum Dosage
Ertugliflozin 15 mg/day PO and metformin 2,000 mg/day PO.
Ertugliflozin 15 mg/day PO and metformin 2,000 mg/day PO.
Safety and efficacy have not been established.
Safety and efficacy have not been established.
Not indicated.
Not indicated.
How supplied
Ertugliflozin/Metformin
tablet
- 2.5mg/500mg
- 2.5mg/1000mg
- 7.5mg/500mg
- 7.5mg/1000mg