Product image of Glurenorm (Gliquidone) supplied by GNH India

Glurenorm

Active Ingredient:
Gliquidone
Origin:
EU

Glurenorm (Gliquidone)

Glurenorm is an oral tablet containing the sulfonylurea gliquidone; the specific strength is not disclosed in the available data. It is a prescription medication marketed in the European Union for the management of type 2 diabetes mellitus. As a second‑generation sulfonylurea, Glurenorm works by stimulating insulin release from pancreatic β‑cells. It belongs to ATC code A10BB04 and is classified as an oral hypoglycemic agent.

Manufacturer / TM Owner

Boehringer Ingelheim International Gmbh

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Indications & Clinical Uses

Glurenorm (gliquidone) is indicated for the treatment of type 2 diabetes mellitus when diet, exercise, and other oral agents are insufficient to achieve glycemic control. It may be used as monotherapy or in combination with other antidiabetic drugs as part of a comprehensive management plan.

  • Initiate therapy in adults with inadequate glycemic control.
  • Add to metformin when monotherapy does not achieve target HbA1c.
  • Combine with basal insulin for patients requiring intensified treatment.
  • Use in patients with preserved pancreatic β‑cell function.
  • Adjust dose based on renal function and hypoglycemia risk.

Side Effects

The safety profile of Glurenorm reflects the typical effects of second‑generation sulfonylureas, with both frequent mild reactions and rarer serious events.

Common

  • Mild hypoglycemia, especially with missed meals.
  • Nausea or abdominal discomfort.
  • Headache or dizziness.
  • Weight gain due to increased insulin activity.
  • Diarrhea.

Serious

  • Severe hypoglycemia leading to loss of consciousness.
  • Allergic skin reactions such as rash or urticaria.
  • Hepatic dysfunction indicated by elevated transaminases.
  • Hematologic abnormalities like leukopenia or thrombocytopenia.
  • Pancreatitis.

Precautions & Warnings

When prescribing Glurenorm, clinicians should evaluate patient-specific factors that may increase the risk of adverse outcomes or reduce therapeutic effectiveness.

  • Assess renal and hepatic function before initiation and during therapy.
  • Use caution in elderly patients due to heightened hypoglycemia susceptibility.
  • Avoid use in patients with known sulfonylurea hypersensitivity.
  • Monitor blood glucose closely during periods of fasting or altered diet.
  • Adjust dose or discontinue if recurrent hypoglycemia occurs.
  • Counsel patients on recognizing early signs of low blood sugar.
  • Consider pregnancy status; safety data are limited.

Avoid Interactions

Glurenorm can interact with several medicines that affect glucose metabolism or sulfonylurea clearance, potentially altering its efficacy or safety.

Avoid

  • Concurrent use with other sulfonylureas or meglitinides.
  • Strong CYP2C9 inhibitors such as fluconazole or amiodarone.
  • High‑dose aspirin or NSAIDs that may potentiate hypoglycemia.

Use with caution

  • Beta‑blockers, which may mask hypoglycemia symptoms.
  • Thiazide diuretics, which can increase blood glucose levels.
  • Anticoagulants like warfarin, requiring INR monitoring.

Frequently Asked Questions

Glurenorm stimulates insulin secretion by binding to the sulfonylurea receptor on pancreatic β‑cells, closing K‑ATP channels and causing cell depolarization.

Glurenorm is a second‑generation sulfonylurea, which generally provides a longer duration of action and a lower risk of certain adverse effects compared with first‑generation agents.

It is prescribed for adults with type 2 diabetes mellitus who have not achieved adequate glycemic control with diet, exercise, and other oral antidiabetic agents.

Common side effects include mild hypoglycemia, nausea, abdominal discomfort, headache, dizziness, weight gain, and occasional diarrhea.

Symptoms may include sweating, shakiness, rapid heartbeat, hunger, confusion, and irritability. Prompt measurement of blood glucose is recommended if these signs appear.

Yes, Glurenorm is often combined with metformin to improve glycemic control when monotherapy with either agent is insufficient.

Regular monitoring of fasting blood glucose, HbA1c, renal and hepatic function tests, and liver enzymes is advised.

Patients should maintain a consistent carbohydrate intake and avoid skipping meals, as irregular eating patterns can increase the risk of hypoglycemia.

Reduced renal function may increase the risk of hypoglycemia; dose adjustments or increased monitoring are recommended in patients with moderate to severe renal impairment.

If a dose is missed and the next scheduled dose is more than 12 hours away, take the missed dose. Otherwise, skip it and resume the regular dosing schedule.

Safety data for Glurenorm in pregnancy and lactation are limited; it should be used only if the potential benefit justifies the potential risk to the fetus or infant.

Fluconazole is a strong CYP2C9 inhibitor and can increase gliquidone plasma levels, raising the risk of hypoglycemia; dose adjustment or alternative therapy may be needed.

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GNH India Pharmaceuticals Limited

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Last updated:

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