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

Metforem

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metforem (Metformin Hydrochloride)

Metformin, the active ingredient in Metforem, is a Biguanide presented as an oral dosage form for oral use. It is used to improve glycemic control in adults with type 2 diabetes mellitus.

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

Manufacturer / TM Owner

Orion Corporation

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Indications & Clinical Uses

Metforem is a Biguanide that acts on glucose metabolism to manage hyperglycaemia.

  • Type 2 diabetes mellitus: lowers blood glucose by reducing hepatic glucose output and increasing peripheral insulin sensitivity.
  • Prediabetes (impaired fasting glucose): helps delay progression to overt diabetes through improved insulin action.
  • Polycystic ovary syndrome (PCOS): assists in correcting insulin resistance associated with the condition.

How It Works

  • Metformin primarily inhibits mitochondrial respiratory‑chain complex I, decreasing hepatic gluconeogenesis and reducing glucose production. It also enhances insulin‑mediated glucose uptake in skeletal muscle and adipose tissue by activating AMP‑activated protein kinase (AMPK), which improves peripheral insulin sensitivity and promotes utilization of glucose.

Side Effects

Metforem may cause a range of adverse reactions.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhoea: frequent loose stools, especially at treatment initiation.
  • 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 potentially fatal metabolic acidosis.
  • Severe hypoglycaemia: usually when combined with other glucose‑lowering agents.
  • Vitamin B12 deficiency: may develop with long‑term therapy.
  • Hepatic dysfunction: abnormal liver enzymes or hepatitis.
  • Allergic skin reactions: rash, urticaria, or Stevens‑Johnson syndrome.
  • Pancreatitis: inflammation of the pancreas, presenting with abdominal pain.

Precautions & Warnings

Metforem requires careful patient assessment and monitoring.

  • Renal function assessment: avoid or adjust dose in patients with impaired renal clearance.
  • Hepatic function monitoring: use with caution in liver disease.
  • Blood glucose monitoring: regularly check glucose to avoid hypoglycaemia, especially when combined with insulin.
  • Contraindicated in metabolic acidosis: do not use in patients with ketoacidosis or severe acidosis.
  • Use with caution in elderly: increased susceptibility to renal impairment and dehydration.
  • Store at ambient temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate acute renal failure, increasing risk of lactic acidosis.
  • Cimetidine: can raise metformin plasma concentrations, heightening toxicity risk.
  • Alcohol: potentiates lactic acidosis, especially in patients with hepatic disease.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask symptoms of hypoglycaemia.
  • Diuretics (especially thiazides): can affect renal clearance of metformin.
  • ACE inhibitors or ARBs: monitor renal function and electrolytes.
  • Thyroid hormones: may require adjustment of glycaemic control.

Frequently Asked Questions

Metforem contains metformin hydrochloride and is prescribed to improve blood‑sugar control in adults with type 2 diabetes mellitus. It may also be used in prediabetes and to address insulin resistance in conditions such as polycystic ovary syndrome, under medical supervision.

Metformin reduces hepatic glucose production by inhibiting mitochondrial complex I and activates AMP‑activated protein kinase (AMPK). This dual action lowers the amount of glucose released by the liver and increases the uptake of glucose by muscle and fat cells, enhancing overall insulin sensitivity.

The appropriate dose of Metforem is determined by the prescribing clinician based on the individual’s renal function, glycaemic targets, and tolerability. Dosage adjustments are made during treatment to achieve optimal blood‑glucose control while minimizing side effects.

Safety of metformin in pregnancy and lactation should be evaluated by a healthcare professional. While some guidelines allow its use in certain pregnant patients with gestational diabetes, the decision depends on risk‑benefit assessment. Metformin does pass into breast milk in small amounts, so breastfeeding mothers should consult their physician.

To request Metforem, submit an enquiry on the product page at gnhindia.com indicating 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.

Metforem (metformin) belongs to the biguanide class and is often first‑line therapy for type 2 diabetes because of its efficacy, low risk of hypoglycaemia and favourable impact on weight. Compared with sulfonylureas or insulin, metformin does not cause weight gain and has a well‑established safety profile, though it requires renal monitoring.

Metforem should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use it after the expiry date indicated on the label.

Metforem is taken orally, usually with meals to reduce gastrointestinal discomfort. Tablets are swallowed whole with a glass of water. The exact timing and frequency are prescribed by the treating physician based on individual therapeutic goals.

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 muscle pain, rapid breathing, or abdominal discomfort develop.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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