Product image of Jivolar (Metformin Hydrochloride, Sitagliptin) supplied by GNH India

Jivolar

Active Ingredient:
Metformin Hydrochloride, Sitagliptin
Origin:
EU

Jivolar (Metformin Hydrochloride, Sitagliptin)

Metformin Hydrochloride and Sitagliptin, the active ingredient in Jivolar, is a biguanide and DPP‑4 inhibitor presented as a tablet for oral use. It treats type 2 diabetes mellitus in adults.

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

Manufacturer / TM Owner

Medochemie Ltd.

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Indications & Clinical Uses

Jivolar is an oral antidiabetic medication used to improve glycaemic control in type 2 diabetes mellitus.

  • Type 2 diabetes mellitus: lowers fasting and post‑prandial blood glucose levels.
  • Adjunct to diet and exercise: helps patients achieve target HbA1c when lifestyle changes alone are insufficient.
  • Combination therapy: used when metformin or sitagliptin monotherapy does not provide adequate control.

How It Works

  • Metformin Hydrochloride decreases hepatic gluconeogenesis and enhances peripheral insulin sensitivity, while Sitagliptin selectively inhibits dipeptidyl peptidase‑4 (DPP‑4), prolonging endogenous incretin activity and promoting glucose‑dependent insulin secretion, together resulting in reduced blood glucose concentrations.

Side Effects

Common Side Effects

  • Gastrointestinal upset: nausea, abdominal discomfort, or diarrhea.
  • Headache: mild to moderate intensity.
  • Mild hypoglycaemia: especially when combined with other glucose‑lowering agents.

Serious or Rare Side Effects

  • Lactic acidosis: a rare but potentially fatal metabolic complication.
  • Severe hypoglycaemia: can occur with concomitant insulin or sulfonylureas.
  • Pancreatitis: acute inflammation of the pancreas.
  • Allergic reactions: rash, angioedema, or anaphylaxis.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Jivolar should be used with careful monitoring of renal and hepatic function and awareness of hypoglycaemia risk.

  • Renal function monitoring: assess eGFR before initiation and periodically thereafter.
  • Hepatic function monitoring: evaluate liver enzymes at baseline and during therapy.
  • Risk of lactic acidosis: avoid in patients with severe renal impairment or acute heart failure.
  • Use with caution in elderly patients: increased susceptibility to adverse events.
  • Contraindicated in severe heart failure: may exacerbate metabolic acidosis.
  • Store at room temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Jivolar may interact with several drug classes, requiring dose adjustments or monitoring.

Major Interactions (Avoid)

  • Other biguanides (e.g., phenformin): increase risk of lactic acidosis.
  • Insulin secretagogues (sulfonylureas, meglitinides): potentiate hypoglycaemia.
  • Iodinated contrast agents: may precipitate acute renal failure.
  • Alcohol excess: heightens lactic acidosis risk.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): raise sitagliptin levels.

Moderate Interactions (Monitor Closely)

  • Diuretics (thiazides, loop diuretics): affect renal clearance of metformin.
  • ACE inhibitors/ARBs: combined impact on renal function.
  • NSAIDs: may reduce renal perfusion, increasing metformin accumulation.
  • Beta‑blockers: can mask hypoglycaemia symptoms.
  • Warfarin: monitor INR as sitagliptin may alter anticoagulant effect.

Frequently Asked Questions

Jivolar is prescribed to improve blood glucose control in adults with type 2 diabetes mellitus, often as part of a regimen that includes diet, exercise, and other antidiabetic agents.

Metformin reduces hepatic glucose production and increases insulin sensitivity, while Sitagliptin blocks the DPP‑4 enzyme, prolonging incretin activity and enhancing glucose‑dependent insulin release, together lowering blood sugar levels.

The specific dose of Jivolar is determined by the prescribing healthcare professional based on individual patient factors such as renal function, glycaemic targets, and concomitant medications.

Safety of Jivolar in pregnancy or lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and under close medical supervision.

Submit an enquiry on the product page at gnhindia.com with 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 import documentation.

Jivolar combines a biguanide (metformin) with a DPP‑4 inhibitor (sitagliptin), offering dual mechanisms of action. Compared with metformin alone, it provides greater HbA1c reduction, and versus DPP‑4 inhibitor monotherapy, it adds the insulin‑sensitising effect of metformin.

Store Jivolar at room temperature, below 25 °C, in the original packaging, and protect it from moisture and direct sunlight to maintain product stability.

Jivolar is taken orally, usually once daily with or after a meal, as directed by the prescriber. Swallow the tablet whole with water; do not crush or chew unless specifically instructed.

The most serious risks include lactic acidosis (rare but life‑threatening) and severe hypoglycaemia, especially when used with insulin or sulfonylureas. Prompt medical attention is required if symptoms of these conditions appear.

Jivolar is contraindicated in patients with severe renal impairment, acute or chronic metabolic acidosis, known hypersensitivity to metformin or sitagliptin, and those with severe heart failure. A healthcare professional should evaluate suitability before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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