Product image of Glimepiride Bristol Laboratories (Glimepiride) supplied by GNH India

Glimepiride Bristol Laboratories

Active Ingredient:
Glimepiride
Origin:
EU

Glimepiride Bristol Laboratories (Glimepiride)

Glimepiride Bristol Laboratories is a prescription medication that contains the active ingredient glimepiride, a sulfonylurea class antidiabetic agent, supplied in oral tablet form for the European market. It works by stimulating insulin release from pancreatic beta cells, helping to lower elevated blood glucose levels in patients with type 2 diabetes mellitus. The product is regulated as a prescription‑only drug and does not have a controlled substance schedule.

Manufacturer / TM Owner

Bristol Laboratories Limited

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Indications & Clinical Uses

Glimepiride Bristol Laboratories is indicated for the management of hyperglycemia in adults with type 2 diabetes mellitus, typically as an adjunct to diet and exercise.

  • Monotherapy in patients who cannot achieve glycemic control with diet and exercise alone.
  • Combination therapy with metformin or other oral antidiabetic agents when additional glucose lowering is needed.
  • Use in patients with stable renal function where sulfonylurea therapy is appropriate.
  • May be considered in patients who require a once‑daily oral agent to improve adherence.

Side Effects

The safety profile of glimepiride includes a range of observed adverse events, which are categorized by frequency and clinical significance.

Common

  • Low blood sugar (hypoglycemia), especially when meals are missed or dosing is excessive.
  • Weight gain due to increased insulin activity.
  • Gastrointestinal discomfort such as nausea, abdominal pain, or dyspepsia.
  • Skin reactions like rash or pruritus.

Serious

  • Severe hypoglycemia leading to loss of consciousness or seizures.
  • Allergic reactions including angioedema or Stevens‑Johnson syndrome.
  • Hepatotoxicity manifested by elevated liver enzymes.
  • Hematologic abnormalities such as leukopenia or thrombocytopenia.

Precautions & Warnings

When prescribing glimepiride, clinicians should evaluate several precautionary factors to minimize risk and ensure appropriate use.

  • Assess renal and hepatic function before initiation and monitor periodically.
  • Use caution in elderly patients due to increased susceptibility to hypoglycemia.
  • Avoid use during pregnancy and lactation; the safety profile is not established.
  • Review concomitant medications that may potentiate hypoglycemia, such as beta‑blockers or other sulfonylureas.
  • Adjust dose in patients with a history of cardiovascular disease or heart failure.
  • Counsel patients on recognizing signs of hypoglycemia and the importance of regular meals.

Avoid Interactions

Glimepiride can interact with other medicines, affecting its glucose‑lowering effect or increasing the risk of adverse reactions.

Avoid

  • Other sulfonylureas or meglitinides, which may cause additive hypoglycemia.
  • Strong CYP2C9 inhibitors (e.g., fluconazole, amiodarone) that can raise glimepiride plasma levels.
  • High‑dose salicylates that may potentiate hypoglycemic action.

Use with caution

  • Beta‑blockers, which can mask hypoglycemia symptoms.
  • ACE inhibitors or angiotensin receptor blockers, which may enhance insulin sensitivity.
  • Thiazide diuretics, which can affect glucose metabolism.
  • Alcohol consumption, which may increase hypoglycemia risk.

Frequently Asked Questions

Glimepiride binds to the sulfonylurea receptor on pancreatic beta‑cell ATP‑sensitive potassium channels, causing channel closure, cell depolarization, calcium influx and increased insulin secretion.

It is primarily prescribed for the treatment of type 2 diabetes mellitus to improve glycemic control when diet and exercise alone are insufficient.

No, it is a prescription‑only medication (Rx‑only) and must be prescribed by a qualified healthcare professional.

The safety of glimepiride in pregnancy has not been established; it is generally avoided and alternative treatments are preferred.

Common side effects include hypoglycemia, weight gain, gastrointestinal discomfort such as nausea or abdominal pain, and mild skin reactions like rash.

Serious reactions can include severe hypoglycemia leading to loss of consciousness, allergic reactions such as angioedema, liver enzyme elevations, and blood‑cell abnormalities.

It should be taken once daily with the first main meal of the day, and patients should avoid skipping meals or taking extra doses without medical advice.

Baseline assessment of renal and hepatic function, as well as fasting blood glucose or HbA1c, is recommended before initiating therapy.

Concurrent use of other sulfonylureas, meglitinides, or strong CYP2C9 inhibitors should be avoided due to increased risk of hypoglycemia.

Yes, alcohol can potentiate the hypoglycemic effect of glimepiride and should be consumed with caution or avoided.

Elderly patients may have increased sensitivity to hypoglycemia and may require lower starting doses and close monitoring.

They should seek immediate medical attention, consume fast‑acting carbohydrates if conscious, and inform their healthcare provider about the episode.

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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