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 dipeptidyl peptidase‑4 (DPP‑4) inhibitor presented as a tablet for oral administration. It is indicated for the management of type 2 diabetes mellitus in adult patients, helping to lower elevated blood glucose levels when combined with diet and exercise.

GNH India supplies Jalra as a licensed, Good Distribution Practice (GDP)‑compliant pharmaceutical product, providing reliable international sourcing for hospitals, pharmacies and clinics across global markets. The company ensures product quality, regulatory conformity and timely delivery to meet the needs of healthcare providers worldwide.

Manufacturer / TM Owner

Novartis Europharm Limited

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Indications & Clinical Uses

Vildagliptin is used in the treatment of type 2 diabetes mellitus, a chronic metabolic disorder characterized by insulin resistance and impaired glucose regulation.

  • Type 2 diabetes mellitus: Improves glycemic control when combined with diet, exercise and other antidiabetic agents.
  • Combination with metformin: Enhances overall glucose‑lowering effect in patients requiring dual therapy.
  • Use as add‑on to insulin or sulfonylureas: Provides additional reduction in HbA1c for patients not achieving targets.

How It Works

  • Vildagliptin selectively inhibits the enzyme dipeptidyl peptidase‑4 (DPP‑4), which degrades the incretin hormones GLP‑1 and GIP. By blocking DPP‑4, endogenous GLP‑1 and GIP levels rise, leading to glucose‑dependent stimulation of insulin secretion and suppression of glucagon release from pancreatic α‑cells, thereby lowering post‑prandial and fasting blood glucose concentrations. The effect is glucose‑dependent, minimizing risk of hypoglycaemia when used without insulin secretagogues, and it does not affect gastric emptying or insulin sensitivity directly.

Side Effects

Vildagliptin may be associated with a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: transient cranial discomfort.
  • Dizziness: occasional light‑headedness.
  • Upper respiratory tract infection: symptoms such as sore throat or nasal congestion.
  • Hypoglycaemia (when combined with insulin or sulfonylureas): low blood sugar episodes.

Serious or Rare Side Effects

  • Pancreatitis: severe abdominal pain with elevated enzymes.
  • Severe allergic reactions: rash, angioedema or anaphylaxis.
  • Hepatic dysfunction: abnormal liver enzymes or jaundice.
  • Bullous pemphigoid: skin blistering disorder.
  • Severe hypoglycaemia: prolonged low glucose requiring assistance.

Precautions & Warnings

When prescribing Vildagliptin, clinicians should consider several precautionary measures to ensure safe use.

  • Renal impairment: assess kidney function and adjust dose if necessary.
  • Hepatic impairment: use with caution and monitor liver enzymes.
  • Risk of hypoglycaemia: monitor glucose closely when combined with insulin or sulfonylureas.
  • Pregnancy and lactation: avoid unless benefits outweigh potential risks.
  • Elderly patients: evaluate renal function regularly due to age‑related decline.
  • Store at ambient temperature below 25°C: keep in the original container, protect from moisture.

Avoid Interactions

Vildagliptin can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Concomitant use with insulin secretagogues (e.g., sulfonylureas): may cause severe hypoglycaemia.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): can increase vildagliptin plasma concentrations.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: monitor renal function and potassium levels.
  • Diuretics: watch for electrolyte disturbances.
  • Warfarin: check INR regularly for anticoagulation changes.
  • Rifampin: may reduce vildagliptin effectiveness.
  • Oral contraceptives: possible alteration in hormone levels, monitor efficacy.

Frequently Asked Questions

Jalra contains vildagliptin, a DPP‑4 inhibitor indicated for the treatment of type 2 diabetes mellitus in adult patients. It is used to improve blood‑glucose control when combined with diet, exercise and, when appropriate, other antidiabetic medications.

Vildagliptin blocks the enzyme dipeptidyl peptidase‑4, preventing the breakdown of the incretin hormones GLP‑1 and GIP. Higher incretin levels enhance glucose‑dependent insulin secretion and suppress glucagon release, which together lower fasting and post‑prandial blood glucose concentrations.

The prescribed dose of Jalra is determined by the treating physician based on the individual’s clinical condition, renal function and concomitant therapies. Patients should follow the dosing instructions provided on the prescription label and not adjust the dose without medical advice.

Vildagliptin is not recommended for use in pregnancy or while nursing unless the potential benefit justifies the possible risk to the fetus or infant. Healthcare providers should evaluate alternative treatments and discuss any concerns with the patient.

To request 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 intrinsic risk of hypoglycaemia because its insulin‑stimulating effect is glucose‑dependent. Unlike metformin, it does not affect gastrointestinal absorption, and it can be combined with both agents to achieve additional HbA1c reduction.

Jalra tablets should be stored at ambient temperature below 25 °C, in the original blister pack, protected from moisture and direct sunlight. Keep the medication out of reach of children and do not use after the expiry date.

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

The most serious adverse events linked to vildagliptin include pancreatitis, severe allergic reactions such as anaphylaxis, hepatic dysfunction and rare cases of bullous pemphigoid. Patients should seek immediate medical attention if they experience persistent abdominal pain, rash, jaundice or signs of severe hypersensitivity.

Jalra is contraindicated in patients with a known hypersensitivity to vildagliptin or any excipients in the tablet. It should also be avoided in individuals with severe renal impairment (eGFR < 30 mL/min/1.73 m²) unless dose adjustment is made, and in pregnant or nursing women unless clearly justified.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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