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 prescribed to improve glycemic control in adults with type 2 diabetes mellitus, often in combination with diet, exercise, and other antidiabetic agents.

GNH India supplies Meliglix as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable sourcing for regulated markets. Customers benefit from consistent batch release, comprehensive documentation, and responsive technical support.

Manufacturer / TM Owner

Pharmazac Sa

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Indications & Clinical Uses

Sitagliptin is a DPP-4 inhibitor used to manage hyperglycemia in type 2 diabetes.

  • Type 2 diabetes mellitus (monotherapy): reduces fasting and post‑prandial glucose levels as a single agent.
  • Type 2 diabetes mellitus (combined with metformin): enhances overall glycemic control when added to metformin therapy.
  • Type 2 diabetes mellitus (combined with insulin): may allow reduction of insulin dose while maintaining target glucose levels.

How It Works

  • Sitagliptin selectively inhibits the dipeptidyl peptidase‑4 (DPP‑4) enzyme, preventing the breakdown of endogenous incretin hormones such as GLP‑1 and GIP. Elevated incretin levels increase glucose‑dependent insulin secretion and suppress glucagon release, leading to improved post‑prandial and fasting blood glucose regulation without causing hypoglycemia when used alone.

Side Effects

Adverse reactions reported with sitagliptin vary in frequency and severity.

Common Side Effects

  • Nasopharyngitis: mild upper respiratory tract infection symptoms.
  • Headache: transient mild to moderate headache.
  • Upper respiratory infection: cough, sore throat, or congestion.
  • Nausea: occasional mild nausea.
  • Diarrhea: loose stools that are usually self‑limiting.

Serious or Rare Side Effects

  • Pancreatitis: severe abdominal pain requiring immediate medical attention.
  • Severe allergic reactions: rash, angioedema, or anaphylaxis.
  • Arthralgia: persistent joint pain.
  • Hepatic injury: elevated liver enzymes or hepatitis.
  • Hypoglycemia: when combined with insulin or insulin secretagogues.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety factors.

  • Renal function assessment: dose adjustment may be required in impaired renal function.
  • Monitor for pancreatitis: discontinue if signs of acute pancreatitis appear.
  • Use caution in elderly patients: increased susceptibility to adverse events.
  • Avoid in patients with known hypersensitivity to sitagliptin or other DPP‑4 inhibitors.
  • Assess hepatic function: monitor liver enzymes periodically.
  • Store at ambient temperature: keep below 25 °C in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Sitagliptin may interact with other medicines, requiring attention to potential effects.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase sitagliptin exposure.
  • Strong CYP2C8 inhibitors (e.g., gemfibrozil): can raise plasma concentrations.
  • Insulin secretagogues (e.g., sulfonylureas): heightened risk of hypoglycemia.

Moderate Interactions (Monitor Closely)

  • Diuretics: possible alterations in glucose control.
  • ACE inhibitors: monitor renal function and electrolytes.
  • Rifampin: may reduce sitagliptin effectiveness by inducing metabolism.

Frequently Asked Questions

Meliglix contains sitagliptin, a DPP‑4 inhibitor that is prescribed to improve blood glucose control in adults with type 2 diabetes mellitus, either alone or in combination with other antidiabetic agents such as metformin or insulin.

Sitagliptin blocks the enzyme dipeptidyl peptidase‑4, which normally degrades the incretin hormones GLP‑1 and GIP. By preserving these hormones, the drug enhances glucose‑dependent insulin secretion and reduces glucagon release, leading to lower blood glucose levels.

The appropriate dose of Meliglix is determined by the prescribing healthcare professional based on the patient’s renal function, glycemic 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 justifies the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

To order Meliglix, 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 hypoglycemia when used alone. Unlike insulin, it is an oral agent and does not require injection. It offers a modest reduction in HbA1c and is often chosen for patients needing a weight‑neutral option.

Meliglix should be stored at ambient temperature, preferably below 25 °C, in its original blister or bottle. Keep the product away from moisture, direct sunlight, and excessive heat to maintain its stability and potency.

Meliglix is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed, unless otherwise directed by a healthcare professional.

The most serious risks include pancreatitis, severe allergic reactions such as anaphylaxis, and rare cases of hepatic injury. Patients should seek immediate medical attention if they experience persistent abdominal pain, rash, swelling, or jaundice while on therapy.

Meliglix should not be used by individuals with a known hypersensitivity to sitagliptin or any component of the formulation. Caution is also advised for patients with severe renal impairment, as dose adjustments may be required, and for those with a history of pancreatitis.

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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