Product image of Jansitin (Sitagliptin) supplied by GNH India

Jansitin

Active Ingredient:
Sitagliptin
Origin:
EU

Jansitin (Sitagliptin)

Sitagliptin, the active ingredient in Jansitin, is a dipeptidyl peptidase‑4 (DPP‑4) inhibitor presented as an oral tablet for oral use. It is used to improve glycaemic control in adults with type 2 diabetes mellitus, typically as part of a comprehensive treatment plan that includes diet and exercise.

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

Manufacturer / TM Owner

G.L. Pharma Gmbh

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Indications & Clinical Uses

Sitagliptin is a DPP‑4 inhibitor indicated for managing type 2 diabetes mellitus and related therapeutic pathways.

  • Type 2 diabetes mellitus: lowers blood glucose levels when used with diet and exercise.
  • Combination with metformin: provides additional reduction in HbA1c compared with metformin alone.
  • Combination with insulin: helps achieve target glycaemic control in patients requiring insulin therapy.

How It Works

  • Sitagliptin selectively inhibits the dipeptidyl peptidase‑4 enzyme, which degrades the incretin hormones GLP‑1 and GIP. By preventing this degradation, circulating levels of GLP‑1 and GIP rise, leading to glucose‑dependent stimulation of insulin secretion and suppression of glucagon release, thereby improving post‑prandial and fasting glucose control.

Side Effects

Sitagliptin is generally well tolerated, but adverse reactions can occur.

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.
  • Diarrhoea: 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.
  • Joint pain: unexplained arthralgia that may be persistent.
  • Bullous pemphigoid: rare skin blistering disorder.
  • Hepatic injury: elevated liver enzymes or hepatitis.

Precautions & Warnings

Before initiating sitagliptin therapy, several safety considerations should be reviewed.

  • Renal impairment: assess renal function and adjust dose if necessary.
  • Hepatic impairment: monitor liver enzymes and use with caution.
  • Hypersensitivity: discontinue if signs of allergic reaction appear.
  • Cardiovascular disease: observe for any worsening of heart failure symptoms.
  • Pregnancy and lactation: limited data; prescribe only if potential benefit justifies risk.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Sulfonylureas: increased risk of hypoglycaemia.
  • Insulin: additive glucose‑lowering effect may cause hypoglycaemia.
  • Strong CYP2C8 inhibitors (e.g., gemfibrozil): raise sitagliptin plasma levels.

Moderate Interactions (Monitor Closely)

  • Rifampin: may decrease sitagliptin exposure, reducing efficacy.
  • Diuretics: altered renal clearance may affect drug concentration.
  • ACE inhibitors: monitor renal function when used together.

Frequently Asked Questions

Jansitin contains sitagliptin, a DPP‑4 inhibitor prescribed to improve blood‑sugar control in adults with type 2 diabetes mellitus, usually together with diet, exercise, and other antidiabetic agents as needed.

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, helping to lower blood glucose levels.

The specific dose of Jansitin is determined by the prescribing clinician based on the patient’s renal function, glycaemic targets, and any concomitant therapies. 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 possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To request Jansitin, 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 or insulin, sitagliptin offers glucose‑dependent insulin secretion with a lower risk of hypoglycaemia. Unlike metformin, it does not affect gastrointestinal absorption, making it a useful add‑on for patients who cannot tolerate metformin.

Jansitin should be stored at ambient temperature, 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.

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

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 swelling of the face or throat.

Jansitin is contraindicated in patients with a known hypersensitivity to sitagliptin or any component of the formulation. Caution is also advised for individuals with severe renal impairment, uncontrolled heart failure, or a history of pancreatitis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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