Product image of Glucophage (Metformin Hydrochloride) supplied by GNH India

Glucophage

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Glucophage (Metformin Hydrochloride)

Glucophage is a brand-name medication containing the active ingredient metformin hydrochloride, supplied in oral tablet form (strength varies) and marketed in the European Union. It belongs to the biguanide class of antidiabetic drugs and is prescribed by healthcare professionals for the management of blood glucose levels in adults with type 2 diabetes mellitus. Glucophage is available only with a prescription and is commonly used as a first-line therapy.

Manufacturer / TM Owner

Merck, S.A.

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Indications & Clinical Uses

Glucophage is indicated for the treatment of type 2 diabetes mellitus and is used as part of a comprehensive diabetes management plan.

  • Improves glycemic control when combined with diet and exercise.
  • Can be used as monotherapy in patients with newly diagnosed type 2 diabetes.
  • May be added to insulin or other oral antidiabetic agents when additional glucose lowering is required.
  • Occasionally prescribed off‑label for polycystic ovary syndrome under specialist supervision.
  • Used in renal‑adjusted dosing for patients with mild to moderate kidney impairment, following clinical guidelines.

Side Effects

Side effects of Glucophage vary in frequency; most are mild and transient, while rare reactions may require medical attention.

Common

  • Gastrointestinal upset such as nausea, abdominal discomfort, or diarrhea.
  • Metallic taste in the mouth.
  • Decreased appetite or mild weight loss.
  • Vitamin B12 deficiency with long‑term use.
  • Elevated liver enzymes.

Serious

  • Lactic acidosis, a rare but potentially life‑threatening condition.
  • Severe skin reactions, including Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Persistent or worsening kidney dysfunction.

Precautions & Warnings

Before starting Glucophage, healthcare providers assess several clinical factors to minimize risks and ensure safe use.

  • Assess renal function; contraindicated in severe renal impairment.
  • Evaluate liver disease status, as hepatic dysfunction can increase lactic acidosis risk.
  • Review any history of alcohol abuse, which may potentiate metabolic complications.
  • Monitor for signs of hypoglycemia when used with insulin or sulfonylureas.
  • Adjust dose in elderly patients due to altered pharmacokinetics.
  • Consider vitamin B12 levels during long‑term therapy.
  • Discontinue before any iodinated contrast imaging that may affect kidney function.

Avoid Interactions

Glucophage can interact with other medicines, affecting its efficacy or increasing the risk of adverse events.

Avoid

  • Iodinated contrast agents used for radiographic studies; may precipitate acute kidney injury.
  • Cimetidine, which can raise metformin plasma concentrations.
  • Certain antivirals such as dolutegravir that may increase metformin exposure.

Use with caution

  • Insulin or sulfonylureas, as combined therapy raises hypoglycemia risk.
  • Diuretics that may affect renal clearance of metformin.
  • ACE inhibitors or ARBs in patients with compromised renal function.

Frequently Asked Questions

Glucophage (metformin) decreases hepatic glucose production and improves peripheral insulin sensitivity, helping to lower blood sugar levels.

Glucophage is usually taken with meals to reduce gastrointestinal discomfort; the exact timing should follow the prescribing healthcare professional’s instructions.

Glucophage may be used with dose adjustment in patients with mild to moderate renal impairment, but it is contraindicated in severe renal failure.

Common gastrointestinal side effects include nausea, abdominal discomfort, diarrhea, and a metallic taste in the mouth.

When combined with insulin, Glucophage can increase the risk of hypoglycemia, so blood glucose should be monitored closely.

Alcohol can increase the risk of lactic acidosis with Glucophage; patients are advised to limit alcohol intake and discuss consumption with their clinician.

Long‑term therapy may require periodic monitoring of renal function, liver enzymes, and vitamin B12 levels, as well as regular assessment of blood glucose control.

Yes, prolonged use of Glucophage has been associated with reduced absorption of vitamin B12, and deficiency should be evaluated if symptoms arise.

Serious reactions may include unexplained muscle pain, rapid breathing, abdominal pain, dizziness, or signs of lactic acidosis such as severe fatigue and nausea; immediate medical attention is required.

Glucophage should be stopped at least 48 hours before receiving iodinated contrast agents and resumed only after renal function has been reassessed.

Elderly patients may have reduced renal function; dose adjustments and careful monitoring are recommended to avoid accumulation and adverse effects.

Both contain the same active ingredient, metformin hydrochloride, and have comparable efficacy; differences may exist in inactive excipients, which can affect tolerability in some individuals.

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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