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

Glucophage Sr

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Glucophage Sr (Metformin Hydrochloride)

Glucophage Sr is an oral prescription tablet whose active ingredient is metformin hydrochloride, a biguanide indicated for type 2 diabetes mellitus in patients with inadequate glycemic control. Available in the European Union, the product is supplied in varying tablet strengths and works by reducing hepatic glucose production and enhancing peripheral insulin sensitivity. It is classified under ATC code A10BA02 and is used as part of a broader diabetes management strategy.

Manufacturer / TM Owner

Merck Serono Limited

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Indications & Clinical Uses

Glucophage Sr is prescribed primarily for the management of type 2 diabetes mellitus.

  • As initial monotherapy for adults whose diet and exercise alone do not achieve target glycemic levels.
  • In combination with other oral antidiabetic agents when additional glucose lowering is needed.
  • As adjunct therapy with insulin to improve overall glycemic control.
  • To help reduce the risk of diabetes‑related complications when used as part of a comprehensive treatment plan.
  • Occasionally used off‑label for conditions such as polycystic ovary syndrome under specialist supervision.

Side Effects

Side effects of Glucophage Sr vary in frequency and severity.

Common

  • Gastrointestinal upset, including nausea, vomiting, or abdominal discomfort.
  • Diarrhea or loose stools.
  • Metallic taste in the mouth.
  • Decreased appetite.
  • Mild skin rash or itching.

Serious

  • Lactic acidosis, a rare but potentially life‑threatening metabolic condition.
  • Severe hypoglycemia when combined with other glucose‑lowering drugs.
  • Hepatotoxicity manifested by elevated liver enzymes.
  • Persistent or worsening gastrointestinal symptoms that may indicate intolerance.
  • Allergic reactions such as angioedema or severe skin eruptions.

Precautions & Warnings

Before starting Glucophage Sr, certain precautions should be considered.

  • Assess renal function; avoid use in patients with severe renal impairment.
  • Monitor liver enzymes periodically, especially in patients with existing hepatic disease.
  • Use cautiously in the elderly, who may have reduced renal clearance.
  • Discontinue before any radiographic studies that use iodinated contrast agents.
  • Educate patients about signs of lactic acidosis and advise immediate medical attention if they occur.
  • Review pregnancy and breastfeeding status; the safety profile is not fully established.

Avoid Interactions

Glucophage Sr can interact with several medications, requiring attention to avoid adverse outcomes.

Avoid

  • Iodinated contrast media used in imaging studies, due to risk of acute renal failure.
  • Cimetidine, which may increase metformin plasma concentrations.
  • Certain diuretics that can impair renal function and elevate metformin levels.

Use with caution

  • Alcohol, which may increase the risk of lactic acidosis.
  • Beta‑blockers, as they can mask hypoglycemia symptoms.
  • Other antidiabetic agents, to prevent excessive lowering of blood glucose.
  • Corticosteroids, which may raise blood glucose and affect metformin efficacy.

Frequently Asked Questions

Glucophage Sr contains metformin hydrochloride, which reduces hepatic glucose production and improves peripheral insulin sensitivity, helping to lower blood glucose levels.

Yes, Glucophage Sr is marketed in the EU as a prescription medication for the treatment of type 2 diabetes mellitus.

Glucophage Sr may be used alongside insulin to enhance overall glycemic control, but dosage adjustments and monitoring are recommended by a healthcare professional.

Common side effects include gastrointestinal symptoms such as nausea, diarrhea, abdominal discomfort, a metallic taste, and mild skin rash.

The medication is usually taken with meals to reduce gastrointestinal upset, but patients should follow the specific instructions provided by their prescriber.

Periodic monitoring of renal function, liver enzymes, and blood glucose levels is advised to ensure safe and effective therapy.

Lactic acidosis is a rare but serious condition that can occur if metformin accumulates, especially in patients with impaired kidney function or other risk factors.

Alcohol can increase the risk of lactic acidosis and may affect blood glucose control, so limiting intake is recommended.

The safety of metformin during pregnancy has not been fully established; clinicians should evaluate risks and benefits before prescribing to pregnant patients.

If a dose is missed, take it as soon as remembered unless it is close to the time of the next scheduled dose. Do not double the dose; follow the guidance of a healthcare provider.

Metformin may be associated with modest weight loss in some patients, but it is not approved as a weight‑loss medication.

No specific dietary restrictions are required, but a balanced diet and regular exercise are important components of diabetes management.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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