Product image of Glimepirid Al (Glimepiride) supplied by GNH India

Glimepirid Al

Active Ingredient:
Glimepiride
Origin:
EU

Glimepirid Al (Glimepiride)

Glimepirid Al is a prescription oral medication that contains the active ingredient glimepiride. It is supplied as tablets (strength not specified) and is marketed in the European Union. Glimepiride belongs to the sulfonylurea class of antidiabetic agents and works by stimulating insulin release from pancreatic beta cells to help control blood glucose in adults with type 2 diabetes. The product is intended for use under medical supervision.

Manufacturer / TM Owner

Aliud Pharma Gmbh

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Indications & Clinical Uses

Glimepirid Al is indicated for the management of hyperglycemia in patients with type 2 diabetes mellitus when diet, exercise, and other oral agents are insufficient.

  • As monotherapy in adults with type 2 diabetes inadequately controlled by lifestyle measures.
  • In combination with metformin when additional glucose lowering is required.
  • As part of a fixed‑dose combination regimen with other oral antidiabetic agents.
  • To improve glycemic control in patients who have a preserved pancreatic beta‑cell function.
  • For use in patients who require a once‑daily oral sulfonylurea.

Side Effects

Glimepirid Al may cause a range of adverse effects, most of which are dose‑related and reversible after discontinuation. These events are reported in clinical studies and post‑marketing surveillance.

Common

  • Mild hypoglycemia, especially when meals are skipped or delayed.
  • Nausea or abdominal discomfort.
  • Headache or dizziness.
  • Weight gain due to increased insulin activity.
  • Transient visual disturbances.

Serious

  • Severe hypoglycemia leading to loss of consciousness.
  • Allergic reactions such as rash, pruritus, or angio‑edema.
  • Hematologic abnormalities including leukopenia or thrombocytopenia.
  • Hepatic dysfunction presenting as elevated transaminases.
  • Severe hypoglycemia leading to loss of consciousness.

Precautions & Warnings

Before prescribing Glimepirid Al, clinicians should evaluate patient history and monitor specific conditions to minimize risk.

  • Assess renal and hepatic function; dose adjustment may be required in impairment.
  • Verify that the patient has adequate pancreatic beta‑cell reserve.
  • Caution in elderly patients due to increased susceptibility to hypoglycemia.
  • Avoid use in patients with known sulfonylurea hypersensitivity.
  • Counsel patients on recognizing and managing hypoglycemic episodes.
  • Review concomitant use of alcohol, which can potentiate hypoglycemia.

Avoid Interactions

Glimepirid Al can interact with several medicines, altering its glucose‑lowering effect or increasing the risk of adverse events.

Avoid

  • Concurrent use with other sulfonylureas or insulin, which may cause severe hypoglycemia.
  • Strong CYP2C9 inhibitors such as fluconazole or amiodarone, which can raise glimepiride plasma levels.
  • Discontinuation of beta‑blockers without medical guidance, as they may mask hypoglycemia symptoms.
  • High‑dose corticosteroids, which may counteract the drug’s efficacy.

Use with caution

  • Loop or thiazide diuretics, which can affect blood glucose control.
  • Antifungal agents like itraconazole that moderately inhibit CYP2C9.
  • NSAIDs and aspirin, which may enhance the hypoglycemic effect.
  • Thyroid hormones, which may alter glucose metabolism.

Frequently Asked Questions

Glimepirid Al is a prescription tablet that contains glimepiride, a sulfonylurea that stimulates insulin release from pancreatic beta cells, helping lower blood glucose in type 2 diabetes.

It is intended for adult patients with type 2 diabetes whose blood glucose is not adequately controlled by diet, exercise, or other oral agents, and who have sufficient pancreatic beta‑cell function.

Glimepirid Al is usually taken once daily with the first main meal of the day, but exact timing should follow the prescribing clinician’s instructions.

Common adverse effects include mild hypoglycemia, nausea, abdominal discomfort, headache, dizziness, weight gain, and occasional transient visual disturbances.

Symptoms may include shakiness, sweating, rapid heartbeat, hunger, confusion, or irritability. If these occur, check blood glucose and treat according to medical guidance.

Yes, Glimepirid Al is often combined with metformin when additional glucose‑lowering effect is needed, provided the combination is prescribed by a healthcare professional.

Avoid concurrent use with other sulfonylureas or insulin, strong CYP2C9 inhibitors (e.g., fluconazole, amiodarone), and abrupt discontinuation of beta‑blockers, as these can increase the risk of severe hypoglycemia.

Renal function should be evaluated before starting therapy; dose adjustments may be necessary in patients with moderate to severe renal impairment.

Elderly patients are more prone to hypoglycemia; clinicians should start at the lowest effective dose, monitor blood glucose closely, and educate about hypoglycemia signs.

Alcohol can potentiate the hypoglycemic effect of glimepiride and may mask symptoms; patients should limit alcohol intake and discuss consumption with their prescriber.

Take the missed dose as soon as remembered if it is still the same day; otherwise skip it and resume the regular dosing schedule. Do not double the dose.

The safety of glimepiride in pregnancy has not been established; it should be used only if the potential benefit justifies the potential risk and under close medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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