Product image of Mapoli (Sitagliptin) supplied by GNH India

Mapoli

Active Ingredient:
Sitagliptin
Origin:
EU

Mapoli (Sitagliptin)

Sitagliptin, the active ingredient in Mapoli, is a DPP-4 inhibitor presented as an oral tablet for oral use. It treats type 2 diabetes mellitus in adults by improving blood‑glucose control.

GNH India supplies Mapoli as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Glenmark Pharmaceuticals S.R.O.

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Indications & Clinical Uses

Mapoli (sitagliptin) is used within the antidiabetic therapeutic pathway to manage hyperglycaemia in type 2 diabetes.

  • Type 2 diabetes mellitus: lowers fasting and post‑prandial blood glucose levels.
  • Combination therapy with metformin: provides additive glycaemic control when monotherapy is insufficient.
  • Adjunct to diet and exercise: supports overall diabetes management alongside lifestyle measures.

How It Works

  • Sitagliptin selectively inhibits the dipeptidyl peptidase‑4 (DPP‑4) enzyme, preventing the breakdown of endogenous incretin hormones (GLP‑1 and GIP). Elevated incretin levels enhance glucose‑dependent insulin secretion from pancreatic β‑cells and suppress glucagon release from α‑cells, resulting in improved post‑prandial glucose regulation without causing hypoglycaemia in the absence of other secretagogues.

Side Effects

Adverse reactions may occur with sitagliptin therapy.

Common Side Effects

  • Nasopharyngitis: mild upper‑respiratory tract infection symptoms.
  • Headache: transient cranial discomfort.
  • Gastrointestinal upset: nausea, diarrhoea or abdominal pain.
  • Dizziness: occasional light‑headed sensation.
  • Upper respiratory infection: cough or sore throat.

Serious or Rare Side Effects

  • Pancreatitis: severe abdominal pain requiring immediate medical attention.
  • Severe allergic reactions: rash, angio‑edema or anaphylaxis.
  • Joint pain: unexplained arthralgia that may be persistent.
  • Bullous pemphigoid: rare blistering skin disorder.
  • Hepatic injury: abnormal liver function tests or hepatitis.

Precautions & Warnings

Before initiating sitagliptin, consider the following safety measures.

  • Renal impairment: dose adjustment may be required based on creatinine clearance.
  • Hepatic impairment: monitor liver enzymes in patients with existing liver disease.
  • Cardiovascular disease: use cautiously in patients with a history of heart failure.
  • Elderly patients: start at the lowest effective dose and monitor for adverse events.
  • Pregnancy and breastfeeding: safety not established; avoid unless benefits outweigh risks.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Sitagliptin may interact with other medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): increase sitagliptin exposure.
  • Strong CYP2C8 inhibitors (e.g., gemfibrozil): raise plasma concentrations.
  • Sulfonylureas or insulin secretagogues: heightened risk of hypoglycaemia.

Moderate Interactions (Monitor Closely)

  • Thiazide diuretics: may affect glucose homeostasis.
  • ACE inhibitors or ARBs: monitor renal function and potassium.
  • NSAIDs: potential additive renal stress, especially in compromised patients.

Frequently Asked Questions

Mapoli contains sitagliptin, a DPP‑4 inhibitor indicated for the treatment of type 2 diabetes mellitus. It is prescribed to improve glycaemic control when diet, exercise, and other oral agents are insufficient.

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

The dosage of Mapoli is determined by the prescribing healthcare professional based on the patient’s renal function, glycaemic targets, and concomitant therapies. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety of sitagliptin in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this decision must be made by a qualified clinician.

To place an order, submit an enquiry on the Mapoli 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 required import documentation.

Compared with sulfonylureas, sitagliptin has a lower risk of causing hypoglycaemia because its insulin‑stimulating effect is glucose‑dependent. Unlike metformin, it does not affect gastrointestinal absorption and can be used in patients who are intolerant to metformin, though renal function must be considered.

Mapoli should be stored at ambient temperature, preferably below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use it after the expiry date.

Mapoli 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 healthcare provider.

Serious adverse events include pancreatitis, severe allergic reactions such as anaphylaxis, and rare skin conditions like bullous pemphigoid. Patients should seek immediate medical attention if they experience persistent abdominal pain, rash, or signs of an allergic reaction.

Mapoli is contraindicated in patients with a known hypersensitivity to sitagliptin or any of its excipients. Caution is advised for individuals with severe renal impairment, active pancreatitis, or those taking strong CYP3A4/CYP2C8 inhibitors without dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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