
Metglip2.5 mg+250
Pacific Pharmaceuticals Ltd.
Glipizide + Metformin Hydrochloride is a fixed-dose combination oral antidiabetic indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
Glipizide + Metformin Hydrochloride is a fixed-dose combination oral antidiabetic indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. Its use is classified by evidence strength as follows:
Glipizide + Metformin Hydrochloride is not a substitute for diet, exercise, and lifestyle modification, which remain the foundation of type 2 diabetes management.
The dosage of Glipizide + Metformin Hydrochloride must be individualized by the treating physician based on current antidiabetic therapy, blood glucose control, and tolerability. It should always be taken with meals to reduce gastrointestinal upset and the risk of hypoglycemia.
| Clinical situation | Typical adult dosing |
|---|---|
| Second-line therapy (inadequate control on a sulfonylurea or metformin alone) | Starting dose should not exceed the equivalent doses of glipizide and/or metformin the patient is already taking; commonly initiated at glipizide 2.5 mg/metformin 250 mg or glipizide 2.5 mg/metformin 500 mg once or twice daily with meals. |
| Initial combination therapy (treatment-naive patients unlikely to respond to monotherapy alone) | Usually started at glipizide 2.5 mg/metformin 250 mg once daily with a meal, titrated gradually. |
| Dose titration | Increased in small increments (e.g., no more than one tablet per week), based on blood glucose response, up to a generally accepted maximum of glipizide 20 mg/metformin 2000 mg per day in divided doses. |
Safety and efficacy of Glipizide + Metformin Hydrochloride in patients under 18 years of age have not been established; it is not recommended for pediatric use.
Glipizide + Metformin Hydrochloride is contraindicated in patients with severe renal impairment (see Contraindications) because of the increased risk of metformin-associated lactic acidosis. In patients with mild to moderate renal impairment, use with caution, at a reduced dose, with regular monitoring of renal function.
Glipizide + Metformin Hydrochloride should generally be avoided in patients with clinically significant hepatic disease, as hepatic impairment increases the risk of lactic acidosis (metformin component) and can affect glipizide metabolism.
Glipizide + Metformin Hydrochloride should be taken exactly as prescribed; do not adjust the dose without consulting a physician.
Side effects of Glipizide + Metformin Hydrochloride arise from both its glipizide and metformin components. Common side effects include:
Less common but serious effects include lactic acidosis (see Contraindications and Precautions) and, with long-term use, vitamin B12 deficiency. Seek prompt medical attention for symptoms of severe hypoglycemia (confusion, sweating, palpitations, loss of consciousness) or lactic acidosis (unusual muscle pain, difficulty breathing, unusual tiredness, abdominal pain, feeling cold, dizziness, slow or irregular heartbeat).
Glipizide + Metformin Hydrochloride is contraindicated in patients with:
Boxed warning (metformin component): Glipizide + Metformin Hydrochloride carries a boxed warning for lactic acidosis, a rare but potentially fatal metabolic complication associated with metformin accumulation. Risk factors include renal impairment, sepsis, dehydration, excessive alcohol intake, hepatic impairment, and acute conditions associated with hypoxemia (e.g., acute heart failure, severe infection). Glipizide + Metformin Hydrochloride should be temporarily withheld in acute illness with a risk of dehydration or renal impairment, and before/after procedures using iodinated contrast media (see Interactions).
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