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Glurenorm

Active Ingredient:
Gliquidone
Origin:
EU

Glurenorm (Gliquidone)

Glurenorm is an oral tablet that contains the second‑generation sulfonylurea gliquidone. It is marketed in the European Union as a prescription‑only medication for the management of type 2 diabetes mellitus. The tablet delivers gliquidone to stimulate insulin release from pancreatic β‑cells, helping to lower blood glucose levels. Glurenorm belongs to the therapeutic class of oral hypoglycemics and carries ATC code A10BB04 in clinical practice worldwide today.

Manufacturer / TM Owner

Boehringer Ingelheim International Gmbh

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Indications & Clinical Uses

Glurenorm is indicated for use in adults with type 2 diabetes mellitus when diet, exercise, and other oral agents are insufficient to achieve glycemic control.

  • Improves fasting and post‑prandial blood glucose levels.
  • Can be used as monotherapy or in combination with other antidiabetic agents such as metformin.
  • May be considered when sulfonylurea therapy is appropriate and patient has adequate renal function.
  • Helps reduce HbA1c levels as part of a comprehensive diabetes management plan.
  • Is prescribed when a second‑generation sulfonylurea is preferred over first‑generation agents.

Side Effects

The safety profile of Glurenorm includes both frequent, mild reactions and less common, potentially serious events.

Common

  • Low blood sugar (hypoglycemia), especially if meals are missed.
  • Nausea or gastrointestinal discomfort.
  • Headache or dizziness.
  • Weight gain due to increased insulin activity.

Serious

  • Severe hypoglycemia leading to loss of consciousness.
  • Allergic reactions such as rash, itching, or swelling.
  • Hepatic dysfunction manifested by jaundice or elevated liver enzymes.

Precautions & Warnings

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

  • Assess renal and hepatic function; dose adjustment may be needed in impairment.
  • Use with caution in elderly patients due to increased hypoglycemia risk.
  • Avoid in pregnancy; classified as category C and discontinue if pregnancy occurs.
  • Monitor blood glucose regularly to detect hypoglycemia early.
  • Review concomitant medications that may potentiate hypoglycemia.
  • Caution in patients with a history of cardiovascular disease.
  • Educate patients on recognizing and managing low blood sugar symptoms.

Avoid Interactions

Glurenorm can interact with other drugs, affecting its efficacy or safety.

Avoid

  • Concurrent use with other sulfonylureas or insulin, which may cause severe hypoglycemia.
  • Strong CYP2C9 inhibitors (e.g., fluconazole) that increase gliquidone plasma levels.
  • Discontinuation of beta‑blockers without medical supervision, which can mask hypoglycemia signs.

Use with caution

  • Co‑administration with thiazolidinediones, requiring close glucose monitoring.
  • Use alongside diuretics that may alter electrolyte balance and affect insulin release.
  • Combination with warfarin, as glycemic changes can influence anticoagulant control.

Frequently Asked Questions

Glurenorm gliquidone stimulates insulin secretion by binding to the sulfonylurea receptor (SUR1) on pancreatic β‑cell K‑ATP channels, causing channel closure, cell depolarization, and calcium‑mediated insulin release.

Glurenorm contains gliquidone, a second‑generation sulfonylurea, which generally has a longer duration of action and may require lower doses compared with first‑generation agents.

Glurenorm is contraindicated in patients with known hypersensitivity to gliquidone or other sulfonylureas, in those with severe hepatic impairment, and in individuals with type 1 diabetes.

Common side effects include hypoglycemia, nausea, gastrointestinal discomfort, headache, dizziness, and modest weight gain.

If symptoms of low blood sugar occur, the patient should consume fast‑acting carbohydrates such as glucose tablets or fruit juice, followed by a longer‑acting carbohydrate source, and seek medical advice if symptoms persist.

Glurenorm is classified as pregnancy category C; it should be discontinued during pregnancy and only used if the potential benefit justifies the risk. It is not recommended while breastfeeding.

Routine monitoring of fasting blood glucose, HbA1c, renal and hepatic function tests, and liver enzymes is recommended to assess efficacy and safety.

Renal impairment may increase the risk of hypoglycemia; dose adjustments or alternative therapies should be considered based on the severity of renal dysfunction.

Medications that may cause severe hypoglycemia, such as other sulfonylureas, insulin, and strong CYP2C9 inhibitors, should be avoided or used only under close medical supervision.

No, Glurenorm is a prescription‑only medication and must be prescribed by a qualified healthcare professional.

Glurenorm can affect blood glucose levels, which may indirectly influence warfarin metabolism; regular INR monitoring is advised when both drugs are used together.

The starting dose of Glurenorm should be individualized by a healthcare provider based on the patient’s clinical condition, renal function, and response to therapy.

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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