Product image of Gluctam (Gliclazide) supplied by GNH India

Gluctam

Active Ingredient:
Gliclazide
Origin:
EU

Gluctam (Gliclazide)

Gluctam is a medication that contains the active ingredient gliclazide, a second‑generation sulfonylurea oral antidiabetic drug. It is supplied in tablet form and is marketed in the European Union. Gluctam works by stimulating insulin release from pancreatic beta‑cells, helping to lower blood glucose levels in adults with type 2 diabetes mellitus. The product is prescription‑only and follows EU regulatory standards.

Manufacturer / TM Owner

Egis Pharmaceuticals Plc

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Indications & Clinical Uses

Gluctam is prescribed for the management of type 2 diabetes mellitus when diet, exercise, and other oral agents are insufficient. It is used as part of a comprehensive diabetes care plan that may include lifestyle modification and regular monitoring of blood glucose.

  • Improves glycemic control in adults with type 2 diabetes.
  • Can be combined with metformin or other oral antidiabetic agents.
  • May be used when insulin therapy is not yet required.
  • Supports long‑term reduction of fasting and post‑prandial glucose levels.
  • Often considered after lifestyle measures have not achieved target glucose values.

Side Effects

Side effects of Gluctam vary in frequency and severity. Patients should be aware of both common and potentially serious reactions.

Common

  • Mild hypoglycemia, especially if meals are missed.
  • Gastrointestinal upset such as nausea or abdominal discomfort.
  • Headache or dizziness.
  • Skin rash or mild itching.
  • Weight gain due to improved glucose utilization.

Serious

  • Severe hypoglycemia leading to loss of consciousness.
  • Allergic reactions including swelling of face, lips, or tongue.
  • Hepatic dysfunction indicated by abnormal liver enzymes.
  • Hematologic abnormalities such as leukopenia or thrombocytopenia.
  • Persistent gastrointestinal bleeding.

Precautions & Warnings

Before starting Gluctam, certain health considerations should be reviewed to ensure safe use.

  • Assess renal and hepatic function; dose adjustments may be needed.
  • Use cautiously in elderly patients due to increased hypoglycemia risk.
  • Avoid in patients with known sulfonylurea hypersensitivity.
  • Monitor blood glucose regularly, especially during dose changes.
  • Pregnancy category B: discuss risks and benefits with a healthcare provider.
  • Breastfeeding mothers should consult a physician before use.
  • Discontinue if severe hypoglycemia or allergic reaction occurs.

Avoid Interactions

Gluctam may interact with several drug classes, affecting its efficacy or safety profile.

Avoid

  • Other sulfonylureas or insulin products, which can cause additive hypoglycemia.
  • Strong CYP2C9 inhibitors (e.g., fluconazole, amiodarone) that may increase gliclazide levels.
  • MAO‑B inhibitors, which can potentiate hypoglycemic effects.

Use with caution

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) that may mask hypoglycemia symptoms.
  • Beta‑blockers, which can blunt typical hypoglycemia warning signs.
  • Thiazide diuretics, as they may affect glucose metabolism.
  • Antidepressants such as SSRIs, which have been reported to alter glycemic control.

Frequently Asked Questions

Gluctam contains gliclazide, which binds to the sulfonylurea receptor on pancreatic beta‑cells, closes ATP‑sensitive potassium channels, depolarizes the cell membrane, and triggers calcium influx that stimulates insulin release.

Yes, Gluctam is often combined with metformin to improve glycemic control when lifestyle changes and metformin alone are insufficient.

Common side effects include mild hypoglycemia, gastrointestinal upset, headache, skin rash, and modest weight gain.

Gluctam is taken orally, usually once daily with breakfast, but exact dosing should follow a healthcare provider’s prescription and be adjusted based on blood glucose monitoring.

Gluctam is classified as pregnancy category B in the EU, indicating no evidence of risk in animal studies, but it should only be used during pregnancy if the potential benefit justifies the potential risk.

Severe hypoglycemia, allergic reactions with swelling of the face or tongue, liver dysfunction, and blood disorders such as leukopenia or thrombocytopenia should be evaluated promptly.

Yes, renal function should be assessed because impaired kidneys can increase the risk of hypoglycemia and may necessitate dose adjustments.

NSAIDs may mask some symptoms of hypoglycemia, so patients should use them cautiously and monitor blood glucose closely.

Patients should maintain regular meals and avoid skipping meals, as missed meals increase the risk of hypoglycemia when taking Gluctam.

Frequent blood glucose monitoring is recommended after any dose adjustment to ensure the new dose maintains target glucose levels without causing hypoglycemia.

Elderly patients may be more susceptible to hypoglycemia; therefore, they should start at the lowest effective dose and be monitored closely.

Consume a fast‑acting carbohydrate such as glucose tablets or fruit juice, and recheck blood glucose after 15 minutes. If symptoms persist, seek medical advice.

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GNH India Pharmaceuticals Limited

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Last updated:

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