Product image of Glimepirida Stada (Glimepiride) supplied by GNH India

Glimepirida Stada

Active Ingredient:
Glimepiride
Origin:
EU

Glimepirida Stada (Glimepiride)

Glimepirida Stada is a prescription medication that contains the active ingredient glimepiride, a sulfonylurea antidiabetic agent, supplied as oral tablets. Marketed in the European Union under ATC code A10BB12, it stimulates insulin release from pancreatic beta cells to lower blood glucose in adults with type 2 diabetes mellitus, and is intended to be used together with diet and exercise as part of a personalized management plan.

Manufacturer / TM Owner

Laboratorio Stada, S.L.

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Indications & Clinical Uses

Glimepirida Stada is indicated for the oral treatment of type 2 diabetes mellitus in adults when diet, exercise, and other non‑pharmacologic measures are insufficient to achieve glycemic control.

  • As monotherapy in patients newly diagnosed with type 2 diabetes who do not achieve target glucose levels with lifestyle measures alone.
  • As add‑on therapy to metformin or other oral antidiabetic agents when additional glucose lowering is required.
  • In combination with basal insulin for patients who need further reduction in HbA1c.
  • For patients with stable renal function who can tolerate sulfonylureas.

Side Effects

The safety profile of Glimepirida Stada includes both frequently observed and less common adverse reactions.

Common

  • Mild hypoglycemia manifested by shakiness, sweating, or hunger, usually occurring if a dose is taken without adequate food.
  • Nausea, occasional vomiting, or general abdominal discomfort.
  • Headache of mild to moderate intensity.
  • Dizziness or a sensation of light‑headedness, particularly after standing quickly.

Serious

  • Severe hypoglycemia that may cause confusion, loss of consciousness, or seizures and requires immediate medical attention.
  • Allergic reactions including skin rash, pruritus, urticaria, or angio‑edema that may affect breathing.
  • Hematologic changes such as leukopenia, neutropenia, or thrombocytopenia reported in rare cases.

Precautions & Warnings

Before prescribing Glimepirida Stada, clinicians should evaluate several patient‑specific factors to minimize risk.

  • Assess renal and hepatic function; dose adjustment may be needed in impairment.
  • Review history of cardiovascular disease, as sulfonylureas can affect cardiac ischemic preconditioning.
  • Verify that the patient is not pregnant or breastfeeding; safety data are limited.
  • Caution in elderly patients due to increased susceptibility to hypoglycemia.
  • Avoid use in patients with known hypersensitivity to glimepiride or other sulfonylureas.
  • Monitor for signs of hypoglycemia when initiating therapy or changing dose.

Avoid Interactions

Glimepirida Stada can interact with other medicines, affecting blood glucose levels or increasing the risk of adverse events.

Avoid

  • Concomitant use with other sulfonylureas or insulin that may cause additive hypoglycemia.
  • Strong CYP2C9 inhibitors such as fluconazole or amiodarone, which can raise glimepiride concentrations.

Use with caution

  • Beta‑blockers, which may mask hypoglycemia symptoms.
  • Thiazide diuretics, which can reduce glucose tolerance and require closer monitoring.
  • Antifungal agents like itraconazole or certain macrolide antibiotics that moderately inhibit CYP2C9.
  • Warfarin, as glimepiride may alter INR and require more frequent coagulation monitoring.

Frequently Asked Questions

Glimepirida Stada contains glimepiride, which stimulates insulin release from pancreatic beta cells by closing ATP‑sensitive potassium channels, thereby lowering blood glucose.

Glimepirida Stada is a specific brand of glimepiride; its pharmacologic class is the same as other sulfonylureas, but formulation, dosage strength, and manufacturer may vary.

It is prescribed for adult patients with type 2 diabetes mellitus who have not achieved glycemic targets with diet, exercise, and possibly other oral agents, provided they have adequate renal and hepatic function.

Yes, Glimepirida Stada is commonly added to metformin when additional glucose lowering is needed, provided the combination is monitored for hypoglycemia.

Typical signs include shakiness, sweating, hunger, headache, dizziness, confusion, and in severe cases, loss of consciousness or seizures.

It is usually taken once daily with breakfast; the dose should be taken with food to reduce the risk of hypoglycemia.

Elderly patients have a higher risk of hypoglycemia and may require lower starting doses and closer monitoring of blood glucose.

Blood glucose levels, HbA1c, renal and hepatic function tests, and, in rare cases, complete blood count for hematologic abnormalities should be periodically assessed.

Safety data are limited; the pregnancy category is unknown, so it is generally avoided during pregnancy and lactation unless the benefit outweighs the risk.

Other sulfonylureas, insulin, and strong CYP2C9 inhibitors (e.g., fluconazole, amiodarone) should be avoided due to increased hypoglycemia risk.

Renal impairment may increase drug exposure; dose reduction or careful monitoring is recommended in patients with reduced kidney function.

If a dose is missed, the patient should take it as soon as remembered unless it is near the time of the next scheduled dose; they should not double the dose.

Published by

GNH India Pharmaceuticals Limited

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