Product image of Meliglix (Sitagliptin) supplied by GNH India

Meliglix

Active Ingredient:
Sitagliptin
Origin:
EU

Meliglix (Sitagliptin)

Sitagliptin, the active ingredient in Meliglix, is a DPP-4 inhibitor presented as an oral tablet for oral use. It is indicated for the management of type 2 diabetes mellitus in adult patients, helping to improve glycaemic control when used as part of a comprehensive treatment plan that includes diet and exercise.

GNH India supplies Meliglix as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies, clinics and research institutions worldwide, providing reliable access to quality‑assured medicines across multiple markets.

Manufacturer / TM Owner

Pharmazac Sa

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Indications & Clinical Uses

Meliglix (sitagliptin) is used within the antidiabetic therapeutic pathway to lower blood glucose levels in type 2 diabetes mellitus.

  • Monotherapy: improves glycaemic control when used alone in adults with type 2 diabetes.
  • Combination therapy: enhances glucose lowering when added to metformin or other oral antidiabetics.
  • Adjunct therapy: supports glycaemic management together with diet, exercise and lifestyle modifications.

How It Works

  • Sitagliptin selectively inhibits the dipeptidyl peptidase‑4 (DPP‑4) enzyme, which results in prolonged activity of incretin hormones (GLP‑1 and GIP). The increased incretin levels enhance glucose‑dependent insulin secretion and suppress glucagon release, thereby lowering post‑prandial and fasting plasma glucose concentrations without causing hypoglycaemia when used alone.

Side Effects

Meliglix is generally well tolerated, but a range of adverse reactions have been reported.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Headache: transient cranial discomfort.
  • Nasopharyngitis: common cold‑like symptoms.
  • Upper respiratory tract infection: mild cough or sore throat.
  • Diarrhoea: loose stools, usually self‑limiting.

Serious or Rare Side Effects

  • Pancreatitis: severe abdominal pain requiring immediate medical attention.
  • Severe allergic reactions: rash, angioedema or anaphylaxis.
  • Joint pain: unexplained arthralgia, sometimes persistent.
  • Hepatic injury: elevated liver enzymes or hepatitis.
  • Severe hypoglycaemia: when combined with insulin or sulfonylureas.

Precautions & Warnings

Before initiating Meliglix, clinicians should evaluate several safety considerations.

  • Renal function: assess creatinine clearance and adjust dose if necessary.
  • Hepatic function: monitor liver enzymes in patients with existing liver disease.
  • Hypersensitivity: discontinue immediately if signs of allergic reaction appear.
  • Pregnancy: use only if potential benefit justifies the risk to the fetus.
  • Elderly patients: consider lower starting dose due to possible renal decline.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Meliglix may interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase sitagliptin exposure.
  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Insulin or sulfonylureas: heightened risk of hypoglycaemia, monitor glucose levels.
  • Diuretics (e.g., thiazides): may affect renal clearance of sitagliptin.
  • Digoxin: slight increase in serum concentrations, observe for toxicity.
  • Warfarin: monitor INR as occasional alterations have been reported.

Frequently Asked Questions

Meliglix contains sitagliptin, a DPP‑4 inhibitor that is prescribed to improve blood‑sugar control in adults with type 2 diabetes mellitus, typically as part of a regimen that includes diet, exercise and possibly other antidiabetic agents.

Sitagliptin blocks the enzyme dipeptidyl peptidase‑4, which prolongs the activity of the incretin hormones GLP‑1 and GIP. This enhances glucose‑dependent insulin secretion and reduces glucagon release, leading to lower plasma glucose levels after meals and during fasting.

The appropriate dose of Meliglix is determined by the prescribing healthcare professional based on the individual’s renal function, glycaemic targets and any concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for sitagliptin in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Compared with sulfonylureas, sitagliptin has a lower risk of causing hypoglycaemia when used alone. Unlike insulin, it is an oral agent and does not require injection. It is often used when metformin alone does not achieve target glycaemic control, offering a complementary mechanism of action.

Meliglix should be stored at ambient temperature, below 25 °C, in its original blister pack or container. Protect the tablets from moisture, excessive heat and direct sunlight to maintain potency throughout the shelf life.

Meliglix is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water. Patients should follow the dosing schedule prescribed by their clinician.

Serious adverse events, though rare, include pancreatitis, severe allergic reactions such as anaphylaxis, and joint pain that may be persistent. Patients should seek immediate medical attention if they experience severe abdominal pain, rash, swelling or unexplained arthralgia.

Meliglix is contraindicated in individuals with a known hypersensitivity to sitagliptin or any of the tablet’s excipients. Caution is advised for patients with severe renal impairment, active pancreatitis, or those who are pregnant or breastfeeding without a clear benefit-risk assessment.

Medically reviewed by

Dr. Shweta Ashok More

M.Pharm (Quality Assurance), Ph.D. (Medicinal Chemistry), GNH India Pharmaceuticals Limited · Reviewed 9 Sep 2026

Published by GNH India Pharmaceuticals Limited · Last updated

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