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

Glucophage Xr

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Glucophage Xr (Metformin Hydrochloride)

Glucophage XR is an extended‑release oral tablet containing the active ingredient metformin hydrochloride, marketed in the European Union. It belongs to the biguanide class of antidiabetic agents and is prescribed by health‑care professionals for the management of type 2 diabetes mellitus. The formulation provides a gradual release of metformin, allowing once‑daily dosing and improved gastrointestinal tolerability compared with immediate‑release versions. It requires a prescription and should be taken with food.

Manufacturer / TM Owner

Merck Santé S.A.S.

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Indications & Clinical Uses

Glucophage XR is indicated for the long‑term control of blood glucose in adults with type 2 diabetes mellitus, usually as part of a comprehensive treatment plan that includes diet and exercise.

  • As monotherapy in patients newly diagnosed with type 2 diabetes when metformin is appropriate.
  • In combination with other oral antidiabetic agents (e.g., sulfonylureas, DPP‑4 inhibitors) to achieve glycemic targets.
  • As an adjunct to insulin therapy when additional glucose lowering is needed.
  • For patients who benefit from once‑daily dosing and reduced gastrointestinal side effects compared with immediate‑release metformin.

Side Effects

The safety profile of Glucophage XR reflects the known effects of metformin, with most patients experiencing mild, transient symptoms.

Common

  • Nausea or upset stomach.
  • Diarrhea or loose stools.
  • Abdominal discomfort or bloating.
  • Metallic taste in the mouth.
  • Decreased appetite.

Serious

  • Lactic acidosis, a rare but life‑threatening condition.
  • Severe skin reactions such as Stevens‑Johnson syndrome.
  • Persistent vomiting leading to dehydration.
  • Marked decrease in vitamin B12 levels over long‑term use.

Precautions & Warnings

Before initiating Glucophage XR, health‑care providers assess several clinical factors to ensure safe use and to minimize risk.

  • Assess renal function; avoid use if eGFR is below the recommended threshold.
  • Evaluate hepatic function, as liver disease may increase lactic acidosis risk.
  • Review any history of alcohol abuse, which can potentiate metformin‑associated acidosis.
  • Consider vitamin B12 monitoring during prolonged therapy.
  • Use caution in elderly patients due to reduced renal clearance.
  • Discontinue before any radiographic study using iodinated contrast agents.

Avoid Interactions

Glucophage XR may interact with other medicines, affecting its efficacy or safety.

Avoid

  • Iodinated contrast agents used for imaging studies.
  • Cimetidine, which can increase metformin plasma concentrations.

Use with caution

  • Diuretics that may affect kidney function.
  • ACE inhibitors or ARBs, especially in patients with renal impairment.
  • Certain antiretroviral drugs (e.g., dolutegravir) that can alter metformin clearance.
  • Beta‑blockers that may mask hypoglycemia symptoms.

Frequently Asked Questions

Glucophage XR contains metformin hydrochloride, which reduces hepatic glucose production and improves peripheral insulin sensitivity, helping lower blood glucose levels in type 2 diabetes.

Glucophage XR is formulated for once‑daily oral administration, typically taken with the evening meal to enhance gastrointestinal tolerance.

Renal function must be evaluated before prescribing Glucophage XR; it is contraindicated in patients with severely reduced eGFR because of the risk of lactic acidosis.

Alcohol can increase the risk of lactic acidosis with metformin, so patients are advised to limit alcohol consumption and discuss any intake with their health‑care provider.

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.

Metformin, including the extended‑release formulation, may be associated with modest weight loss in some patients, but it is not approved specifically for weight management.

There are no specific food restrictions, but taking the tablet with a meal can reduce gastrointestinal side effects.

Glucophage XR is classified as pregnancy category B, indicating that animal studies have not shown risk, but it should only be used during pregnancy if clearly needed and prescribed by a physician.

Regular monitoring of blood glucose, renal function, and occasionally vitamin B12 levels is recommended during long‑term therapy.

Glucophage XR releases metformin slowly over time, allowing once‑daily dosing and often resulting in fewer gastrointestinal adverse effects compared with immediate‑release formulations taken multiple times daily.

No, Glucophage XR is a prescription‑only medication and must be prescribed by a qualified health‑care professional.

Inform your doctor about any kidney or liver disease, alcohol use, current medications, pregnancy or breastfeeding status, and any history of allergic reactions to metformin.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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