Product image of Glucovance (Metformin Hydrochloride, Glibenclamide) supplied by GNH India

Glucovance

Active Ingredient:
Metformin Hydrochloride, Glibenclamide
Origin:
EU

Glucovance (Metformin Hydrochloride, Glibenclamide)

Glucovance is a prescription oral medication that combines metformin hydrochloride and glibenclamide in a single tablet. It belongs to the biguanide and sulfonylurea drug classes and is used to improve blood glucose control in adults with type 2 diabetes mellitus. The product is marketed in the European Union and is available only with a doctor's prescription. It is taken orally with meals to lessen stomach upset.

Manufacturer / TM Owner

Merck Santé S.A.S.

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Indications & Clinical Uses

Glucovance is indicated for the management of hyperglycemia in patients with type 2 diabetes mellitus, particularly when diet, exercise, and monotherapy with either metformin or a sulfonylurea have not achieved adequate glycemic control.

  • As adjunct therapy with diet and exercise to lower fasting and post‑prandial blood glucose levels.
  • In combination with lifestyle modifications for patients who require additional glucose‑lowering effect beyond metformin alone.
  • For adults who need both improved insulin sensitivity (metformin) and stimulated insulin secretion (glibenclamide).
  • To simplify treatment regimens by providing two antidiabetic agents in one tablet.

Side Effects

The safety profile of Glucovance reflects the combined actions of metformin and glibenclamide, producing both typical gastrointestinal effects and hypoglycemia‑related reactions.

Common

  • Nausea, abdominal discomfort, or diarrhea.
  • Loss of appetite.
  • Mild headache.
  • Weight gain or mild fluid retention.

Serious

  • Severe hypoglycemia with symptoms such as sweating, shakiness, confusion, or loss of consciousness.
  • Lactic acidosis, a rare but life‑threatening condition characterized by rapid breathing and muscle pain.
  • Allergic skin reactions including rash, itching, or swelling.
  • Hepatic dysfunction indicated by jaundice or elevated liver enzymes.

Precautions & Warnings

When prescribing Glucovance, clinicians should evaluate patient history and monitor for conditions that may increase the risk of adverse events or reduce therapeutic effectiveness.

  • Assess renal function before initiation and periodically, as metformin accumulation can occur in impaired kidneys.
  • Use caution in patients with hepatic disease, heart failure, or a history of lactic acidosis.
  • Monitor blood glucose closely to avoid hypoglycemia, especially when starting therapy or adjusting dose.
  • Avoid use during pregnancy and lactation unless the potential benefit outweighs risks.
  • Review concomitant medications that affect sulfonylurea metabolism or increase hypoglycemia risk.
  • Adjust dose in elderly patients due to altered pharmacokinetics.

Avoid Interactions

Glucovance may interact with several drugs that alter glucose metabolism, renal clearance, or sulfonylurea activity, requiring careful medication review.

Avoid

  • Concurrent use with other sulfonylureas or meglitinides, which can potentiate hypoglycemia.
  • Strong CYP2C9 inhibitors (e.g., fluconazole, amiodarone) that increase glibenclamide plasma levels.
  • Iodinated contrast agents in patients with reduced renal function, due to risk of metformin‑associated lactic acidosis.

Use with caution

  • Beta‑blockers, which may mask hypoglycemia symptoms.
  • Diuretics or ACE inhibitors that affect renal function and electrolyte balance.
  • Alcohol consumption, which can enhance metformin’s effect on lactate metabolism.

Frequently Asked Questions

Glucovance is an oral fixed‑dose combination of metformin hydrochloride and glibenclamide. Metformin reduces hepatic glucose production and improves insulin sensitivity, while glibenclamide stimulates insulin release from pancreatic beta‑cells.

It is prescribed for adults with type 2 diabetes mellitus who need additional glucose control beyond diet, exercise, and monotherapy with either metformin or a sulfonylurea.

Glucovance is generally avoided in pregnancy because the safety of the combination has not been established; alternative treatments are preferred.

Common side effects include gastrointestinal symptoms such as nausea, abdominal discomfort, diarrhea, loss of appetite, mild headache, and modest weight gain.

The glibenclamide component stimulates insulin secretion, which can lower blood glucose excessively, especially if meals are missed or doses are increased.

Lactic acidosis is a rare but serious reaction linked to metformin, characterized by rapid breathing, muscle pain, and elevated lactate levels.

Yes, renal function should be evaluated because impaired kidneys can lead to metformin accumulation and increase the risk of lactic acidosis.

Alcohol should be limited, as it can increase the risk of lactic acidosis and affect blood glucose control.

It can be combined with other agents, but concurrent use with additional sulfonylureas or meglitinides should be avoided due to heightened hypoglycemia risk.

Regular blood glucose checks, periodic assessment of renal and hepatic function, and observation for signs of hypoglycemia or lactic acidosis are recommended.

Elderly patients may require lower starting doses and careful titration because of age‑related changes in drug metabolism and renal function.

Store the tablets at room temperature, away from moisture and heat, and keep them out of reach of children.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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