Product image of Metformin Sr (Metformin Hydrochloride) supplied by GNH India

Metformin Sr

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformin Sr (Metformin Hydrochloride)

Metformin Hydrochloride, the active ingredient in Metformin Sr, is a biguanide presented as an oral tablet for oral use. It is used to lower elevated blood glucose levels in adults with type 2 diabetes mellitus.
GNH India supplies Metformin Sr as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Interdos Pharma Bv.

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Indications & Clinical Uses

Metformin Sr belongs to the biguanide class and is employed in the management of disorders related to glucose metabolism.

  • Type 2 diabetes mellitus: improves glycaemic control by reducing hepatic glucose output and enhancing peripheral insulin sensitivity.
  • Impaired glucose tolerance: helps delay progression to overt diabetes when used as part of lifestyle intervention.
  • Polycystic ovary syndrome (off‑label): may improve insulin resistance and restore ovulatory function.

How It Works

  • Metformin Hydrochloride acts primarily by inhibiting mitochondrial respiratory‑chain complex I, which reduces hepatic gluconeogenesis. It also increases AMP‑activated protein kinase activity, enhancing peripheral glucose uptake and utilization while decreasing intestinal glucose absorption, collectively lowering circulating blood glucose levels.

Side Effects

Metformin Sr 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 of taste perception.
  • Loss of appetite: reduced desire to eat.
  • Flatulence: increased intestinal gas.

Serious or Rare Side Effects

  • Lactic acidosis: rare but life‑threatening metabolic acidosis.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Hypoglycaemia: when combined with other glucose‑lowering agents.
  • Hepatic failure: impaired liver function may exacerbate toxicity.
  • Renal impairment: accumulation leading to toxicity.
  • Vitamin B12 deficiency: long‑term use may reduce absorption.

Precautions & Warnings

Before initiating Metformin Sr, several safety considerations should be observed.

  • Renal function assessment: ensure adequate glomerular filtration rate before prescribing.
  • Hepatic function monitoring: evaluate liver enzymes to reduce lactic acidosis risk.
  • Lactic acidosis risk evaluation: avoid in patients with hypoxia, heart failure, or severe infection.
  • Elderly patient caution: start with lower doses and monitor tolerance.
  • Vitamin B12 status: consider periodic testing during long‑term therapy.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycaemia symptoms.
  • Diuretics: can affect renal clearance of metformin.
  • ACE inhibitors or ARBs: monitor renal function and potassium levels.
  • Warfarin: may require INR monitoring.
  • Digoxin: observe for potential additive effects on renal function.

Frequently Asked Questions

Metformin Sr is an oral antidiabetic medication indicated for the management of type 2 diabetes mellitus. It helps lower elevated blood glucose by decreasing hepatic glucose production and improving insulin sensitivity in peripheral tissues.

Metformin Hydrochloride inhibits mitochondrial respiratory‑chain complex I, reducing hepatic gluconeogenesis. It also activates AMP‑activated protein kinase, which enhances peripheral glucose uptake and utilization while decreasing intestinal glucose absorption, resulting in lower blood glucose levels.

The dose of Metformin Sr is individualized by the prescribing clinician based on the patient’s glycaemic targets, renal function, and tolerability. The prescriber determines the appropriate starting dose and any subsequent titration.

The safety of Metformin Sr in pregnancy and lactation has not been definitively established. Clinicians should weigh potential benefits against possible risks and consider alternative therapies when appropriate.

To place an order, submit an enquiry on the Metformin Sr 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 Sr belongs to the biguanide class and is often first‑line therapy because of its efficacy, low risk of hypoglycaemia and favourable impact on weight. Compared with sulfonylureas or insulin, it does not cause weight gain and has a distinct mechanism targeting hepatic glucose output.

Metformin Sr tablets should be stored at room temperature, below 25 °C, in the original packaging to protect from moisture and light. Keep the container tightly closed and out of reach of children.

Metformin Sr is taken orally, usually with meals to reduce gastrointestinal discomfort. The tablets are swallowed whole with a glass of water; they should not be crushed or chewed unless specifically instructed by a healthcare professional.

The most serious risk is lactic acidosis, a rare but potentially fatal condition that can occur in patients with renal impairment, hepatic disease, or severe hypoxia. Prompt medical attention is required if symptoms such as rapid breathing, muscle pain, or abdominal discomfort develop.

Metformin Sr is contraindicated in patients with severe renal impairment (eGFR < 30 mL/min/1.73 m²), acute or chronic metabolic acidosis, known hypersensitivity to metformin, 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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