Product image of Metformin Hydrochloride Genus Pharmaceuticals (Metformin) supplied by GNH India

Metformin Hydrochloride Genus Pharmaceuticals

Active Ingredient:
Metformin
Origin:
EU

Metformin Hydrochloride Genus Pharmaceuticals (Metformin)

Metformin, the active ingredient in Metformin Hydrochloride Genus Pharmaceuticals, is a biguanide presented as an oral tablet for oral use. It treats type 2 diabetes mellitus by improving blood glucose control in adult patients.

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

Manufacturer / TM Owner

Genus Pharmaceuticals Limited

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Indications & Clinical Uses

Metformin is used primarily in the management of disorders related to impaired glucose regulation.

  • Type 2 diabetes mellitus: improves glycemic control and reduces HbA1c levels.
  • Prediabetes: helps lower fasting glucose and delay progression to diabetes.

How It Works

  • Metformin reduces hepatic gluconeogenesis, decreases intestinal absorption of glucose, and enhances peripheral insulin sensitivity by activating AMP‑activated protein kinase (AMPK). These actions collectively lower circulating glucose concentrations without stimulating insulin secretion, making it effective for chronic hyperglycaemia management.

Side Effects

Metformin may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: loose stools, often transient.
  • Abdominal discomfort: cramping or bloating.
  • Metallic taste: transient alteration of taste perception.
  • Loss of appetite: reduced desire to eat.
  • Weight loss: modest reduction in body weight.

Serious or Rare Side Effects

  • Lactic acidosis: rare but potentially fatal metabolic disturbance.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Hepatic failure: rare liver dysfunction.
  • Vitamin B12 deficiency: may develop with long‑term use.
  • Hypoglycaemia: when combined with other glucose‑lowering agents.

Precautions & Warnings

Metformin requires careful patient assessment and monitoring before and during therapy.

  • Renal function assessment: avoid or adjust dose in patients with impaired renal clearance.
  • Hepatic function monitoring: use cautiously in liver disease.
  • Blood glucose monitoring: regularly check to avoid hypoglycaemia when combined with other agents.
  • Contra‑indication in severe renal impairment: do not initiate in eGFR <30 mL/min/1.73 m².
  • Use with caution in elderly: increased risk of lactic acidosis.
  • Store at ambient temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Metformin can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate acute renal failure and increase lactic acidosis risk.
  • Cimetidine: can raise metformin plasma concentrations.
  • Alcohol: potentiates risk of lactic acidosis.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycaemia symptoms.
  • Diuretics: can affect renal function and metformin clearance.
  • ACE inhibitors: monitor renal function and electrolytes.
  • Calcium channel blockers: may modestly increase metformin levels.
  • Warfarin: occasional reports of altered INR, require monitoring.

Frequently Asked Questions

Metformin Hydrochloride Genus Pharmaceuticals is an oral biguanide indicated for the treatment of type 2 diabetes mellitus and for glycaemic control in individuals with prediabetes. It helps lower blood glucose levels by improving insulin sensitivity and reducing hepatic glucose production.

Metformin acts primarily by activating AMP‑activated protein kinase (AMPK), which suppresses hepatic gluconeogenesis, reduces intestinal glucose absorption, and enhances peripheral insulin sensitivity. These combined effects lower circulating glucose without increasing insulin secretion.

The specific dose of Metformin Hydrochloride is determined by the prescribing clinician based on the patient’s clinical condition, renal function, and response to therapy. Dosage adjustments are made individually and should follow the prescriber’s instructions.

Safety of Metformin during pregnancy or lactation should be evaluated by a healthcare professional. While some guidelines allow its use in certain pregnant patients with diabetes, the decision depends on risk‑benefit assessment, and breastfeeding mothers should consult their physician.

To place an order, 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.

Metformin is often preferred as first‑line therapy for type 2 diabetes because it improves insulin sensitivity without causing weight gain and has a low risk of hypoglycaemia when used alone. Compared with sulfonylureas or insulin, it does not stimulate insulin secretion and therefore carries fewer hypoglycaemic episodes.

Metformin Hydrochloride tablets should be stored at ambient temperature, below 25 °C, in the original container to protect from moisture and light. Keep the product out of reach of children and avoid storing in humid environments.

Metformin Hydrochloride 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 provider.

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

Metformin is contraindicated in patients with severe renal impairment (eGFR <30 mL/min/1.73 m²), known hypersensitivity to metformin, acute or chronic metabolic acidosis, and those receiving iodinated contrast studies without adequate renal function monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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