Product image of Metformine Biogaran (Metformin Hydrochloride) supplied by GNH India

Metformine Biogaran

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformine Biogaran (Metformin Hydrochloride)

Metformin, the active ingredient in Metformine Biogaran, is a Biguanide presented as a tablet for oral use. It treats type 2 diabetes mellitus in adults by improving blood‑glucose control.
GNH India supplies Metformine Biogaran as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Biogaran

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Indications & Clinical Uses

Metformine Biogaran is a Biguanide that targets hyperglycaemia in type 2 diabetes and related metabolic disturbances.

  • Type 2 diabetes mellitus: lowers fasting and post‑prandial blood glucose levels.
  • Insulin resistance: improves peripheral insulin sensitivity.
  • Hepatic glucose output: reduces excessive hepatic glucose production.
  • Glycaemic variability: helps achieve more stable glucose profiles.
  • Cardiovascular risk management: contributes to overall metabolic control in diabetic patients.

How It Works

  • Metformin acts primarily by inhibiting mitochondrial respiratory‑chain complex I, which decreases hepatic gluconeogenesis. It also enhances peripheral glucose uptake by activating AMP‑activated protein kinase (AMPK), reduces intestinal glucose absorption, and improves insulin sensitivity in muscle and adipose tissue, collectively lowering blood glucose concentrations.

Side Effects

Metformine Biogaran may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhoea: loose stools, often early in therapy.
  • Abdominal discomfort: cramping or bloating.
  • Metallic taste: transient alteration in taste perception.
  • Weight loss: modest reduction in body weight.
  • Vitamin B12 deficiency: reduced absorption with long‑term use.

Serious or Rare Side Effects

  • Lactic acidosis: rare but life‑threatening metabolic acidosis.
  • Severe hypoglycaemia: when combined with insulin or sulfonylureas.
  • Hepatic failure: rare hepatic dysfunction.
  • Allergic reactions: rash, pruritus, or angio‑edema.
  • Myopathy: muscle pain or weakness in rare cases.
  • Renal impairment worsening: may precipitate accumulation of the drug.

Precautions & Warnings

Metformine Biogaran requires careful assessment of patient‑specific factors before initiation.

  • Renal function: evaluate eGFR; avoid if severe renal impairment.
  • Lactic acidosis risk: contraindicated in patients with significant cardiac, hepatic, or respiratory disease.
  • Alcohol consumption: limit intake to reduce acidosis risk.
  • Pregnancy: category B; use only when benefits outweigh potential risks.
  • Monitoring: regular HbA1c and renal function tests are recommended.
  • Store at ambient temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Metformine Biogaran can interact with several medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate renal dysfunction and lactic acidosis.
  • Cimetidine: increases metformin plasma concentrations.
  • Alcohol: potentiates risk of lactic acidosis.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycaemia symptoms.
  • Loop diuretics: can affect renal clearance of metformin.
  • ACE inhibitors/ARBs: monitor renal function and electrolytes.
  • Corticosteroids: may raise blood glucose, requiring dose adjustment.
  • Thyroid hormones: may influence glucose metabolism.

Frequently Asked Questions

Metformine Biogaran contains metformin hydrochloride and is used to improve glycaemic control in adults with type 2 diabetes mellitus. It helps lower fasting and post‑prandial blood glucose levels by targeting hepatic glucose production and enhancing insulin sensitivity.

Metformin primarily inhibits mitochondrial complex I, which reduces hepatic gluconeogenesis. It also activates AMP‑activated protein kinase (AMPK), leading to increased peripheral glucose uptake and decreased intestinal glucose absorption, collectively lowering blood glucose concentrations.

The specific dose of Metformine Biogaran is determined by the prescribing healthcare professional based on the individual’s clinical condition, renal function, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Metformine Biogaran is classified as pregnancy category B, indicating that animal studies have not shown risk but there are limited human data. It may be used during pregnancy only if the potential benefit justifies the potential risk. Metformin is excreted in breast milk; breastfeeding decisions should be made in consultation with a healthcare provider.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide. After submission, the sales team will verify trade or institutional credentials and respond with pricing, availability, shipping details and any required import documentation.

Metformine Biogaran belongs to the biguanide class, which differs from sulfonylureas, DPP‑4 inhibitors, or SGLT2 inhibitors. Unlike insulin‑secretagogues, metformin does not stimulate insulin release, reducing the risk of hypoglycaemia when used alone. It also offers benefits such as modest weight loss and potential cardiovascular protection, making it a first‑line therapy in many guidelines.

Metformine Biogaran should be stored at ambient temperature, below 25 °C. Keep the tablets in the original container, protect them from moisture and direct sunlight, and ensure the packaging remains tightly closed until use.

Metformine Biogaran is taken orally, usually with meals to minimise gastrointestinal discomfort. The tablets are swallowed whole with a glass of water. Patients should follow the dosing schedule prescribed by their healthcare professional.

The most serious adverse reaction is lactic acidosis, a rare but potentially fatal condition that can occur in patients with severe renal impairment, hepatic disease, or excessive alcohol intake. Prompt medical attention is required if symptoms such as unexplained fatigue, rapid breathing, or abdominal pain develop.

Metformine Biogaran is contraindicated in patients with severe renal impairment (eGFR < 30 mL/min/1.73 m²), known hypersensitivity to metformin, acute or chronic metabolic acidosis, including diabetic ketoacidosis, and in those with severe hepatic disease. It should also be used with caution in elderly patients and those with heart failure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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