Product image of Jalra (Vildagliptin) supplied by GNH India

Jalra

Active Ingredient:
Vildagliptin
Origin:
EU

Jalra (Vildagliptin)

Vildagliptin, the active ingredient in Jalra, is a DPP-4 inhibitor presented as a tablet for oral use. It is used to improve glycemic control in adults with type 2 diabetes mellitus.

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

Manufacturer / TM Owner

Novartis Europharm Limited

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Indications & Clinical Uses

Jalra (vildagliptin) is indicated for the management of type 2 diabetes mellitus, a condition characterized by impaired insulin secretion and increased glucagon production.

  • Type 2 diabetes mellitus: improves blood glucose control by enhancing insulin release and reducing glucagon.
  • Monotherapy in type 2 diabetes: lowers HbA1c when used alone alongside diet and exercise.
  • Combination therapy with metformin: provides additional reduction in fasting plasma glucose and HbA1c.

How It Works

  • Vildagliptin selectively inhibits the dipeptidyl peptidase‑4 (DPP‑4) enzyme, which degrades the incretin hormones GLP‑1 and GIP. By preventing this degradation, vildagliptin increases circulating incretin levels, leading to glucose‑dependent stimulation of insulin secretion and suppression of glucagon release, thereby improving post‑prandial and overall glycemic control.

Side Effects

Common Side Effects

  • Nausea: mild to moderate gastrointestinal discomfort.
  • Headache: transient cranial pain.
  • Dizziness: occasional light‑headedness.
  • Upper respiratory tract infection: nasopharyngitis or mild cough.
  • Hypoglycemia (when combined with sulfonylureas or insulin): low blood sugar episodes.

Serious or Rare Side Effects

  • Pancreatitis: severe abdominal pain requiring medical attention.
  • Severe allergic reactions: rash, angioedema, or anaphylaxis.
  • Hepatic injury: elevated liver enzymes or hepatitis.
  • Bullous skin disorders: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Severe hypoglycemia: prolonged low glucose requiring assistance.

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor for adverse events.

  • Renal function: assess creatinine clearance and adjust dose in impairment.
  • Hepatic function: evaluate liver enzymes prior to use.
  • Pancreatitis risk: discontinue if severe abdominal pain occurs.
  • Concomitant sulfonylureas or insulin: monitor blood glucose closely to avoid hypoglycemia.
  • Elderly patients: start at lower dose and titrate cautiously.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Vildagliptin may interact with several co‑administered medicines, requiring clinical awareness.

Major Interactions (Avoid)

  • Other DPP‑4 inhibitors: additive inhibition may increase risk of adverse effects.
  • Insulin or sulfonylureas: heightened risk of severe hypoglycemia.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may affect renal function, especially in patients with existing renal impairment.
  • Diuretics: monitor electrolytes and renal parameters.
  • ACE inhibitors or ARBs: watch for changes in blood pressure and renal function.
  • Warfarin: occasional reports of altered INR, require periodic monitoring.

Frequently Asked Questions

Jalra contains vildagliptin, a DPP‑4 inhibitor indicated for improving blood glucose control in adults with type 2 diabetes mellitus, usually as part of a comprehensive treatment plan that includes diet and exercise.

Vildagliptin blocks the DPP‑4 enzyme, which normally breaks down 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 prescribed dose of Jalra is determined by the treating physician based on individual patient factors such as renal function, glycemic targets, and concomitant therapies. Patients should follow the exact dosing instructions provided by their healthcare professional.

The safety of vildagliptin 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 healthcare provider.

To order Jalra, 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, vildagliptin has a lower risk of causing hypoglycemia when used alone. Unlike metformin, it does not affect gastrointestinal absorption. It belongs to the DPP‑4 inhibitor class, offering a glucose‑dependent mechanism that complements many other oral antidiabetic agents.

Jalra tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Do not store in humid or excessively hot environments.

Jalra is taken orally, usually once daily with or without food, as directed by the prescribing clinician. The tablet should be swallowed whole with water and not crushed or chewed unless specifically instructed.

Serious risks include pancreatitis, severe allergic reactions such as anaphylaxis, and rare hepatic injury. Patients should seek immediate medical attention if they experience persistent abdominal pain, rash, swelling, or signs of liver dysfunction.

Jalra is contraindicated in patients with a known hypersensitivity to vildagliptin or any component of the formulation. Caution is also advised for individuals with severe renal impairment, hepatic disease, or a history of pancreatitis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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