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

Metformin Al

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformin Al (Metformin Hydrochloride)

Metformin Hydrochloride, the active ingredient in Metformin Al, is a biguanide presented as an oral dosage form for oral use. It treats type 2 diabetes mellitus in adult patients by improving blood‑glucose control.
GNH India supplies Metformin Al as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Aliud Pharma Gmbh

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Indications & Clinical Uses

  • Metformin Al is a biguanide that lowers elevated blood glucose in disorders of glucose metabolism.
  • Type 2 diabetes mellitus: improves glycemic control by reducing hepatic glucose output and enhancing peripheral insulin sensitivity.
  • Prediabetes: helps delay progression to diabetes by modestly lowering fasting glucose levels.
  • Polycystic ovary syndrome (off‑label): may improve insulin resistance and menstrual regularity in affected women.

How It Works

  • Metformin Hydrochloride primarily inhibits mitochondrial respiratory‑chain complex I, decreasing hepatic gluconeogenesis. It also reduces intestinal glucose absorption and increases peripheral tissue uptake of glucose by enhancing insulin receptor signaling, leading to lower fasting and post‑prandial blood glucose concentrations.

Side Effects

Metformin Al may cause a range of adverse reactions.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: 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.
  • Vitamin B12 deficiency: gradual decrease with long‑term use.

Serious or Rare Side Effects

  • Lactic acidosis: life‑threatening accumulation of lactate, especially in renal impairment.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Hepatotoxicity: rare liver enzyme elevations.
  • Hypoglycemia: when combined with other glucose‑lowering agents.
  • Pancreatitis: very uncommon inflammation of the pancreas.

Precautions & Warnings

  • Metformin Al requires careful consideration of patient‑specific factors before and during therapy.
  • Renal function: assess eGFR before initiating and monitor periodically.
  • Liver disease: use with caution in patients with hepatic impairment.
  • Alcohol consumption: avoid excessive intake due to increased lactic acidosis risk.
  • Pregnancy: discuss potential risks with a healthcare provider; safety category is unknown.
  • Elderly patients: monitor renal function and hydration status closely.
  • Store at ambient temperature: keep below 25°C, retain original packaging, and protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate acute renal failure; discontinue metformin before imaging.
  • Cimetidine: can increase metformin plasma concentrations.
  • Alcohol: potentiates risk of lactic acidosis.
  • Renin‑angiotensin system inhibitors: may affect renal function and metformin clearance.
  • Nucleoside reverse transcriptase inhibitors: increase metformin levels.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycemia symptoms.
  • Thiazide diuretics: can raise blood glucose.
  • Corticosteroids: may reduce metformin’s glucose‑lowering effect.
  • Sulfonylureas: increase risk of hypoglycemia when combined.
  • GLP‑1 receptor agonists: additive glucose‑lowering effect requiring monitoring.

Frequently Asked Questions

Metformin Al is a generic formulation of metformin hydrochloride indicated for the management of type 2 diabetes mellitus. It helps lower elevated blood glucose by decreasing liver glucose production and improving the body's response to insulin.

Metformin Hydrochloride acts mainly by inhibiting mitochondrial complex I, which reduces hepatic gluconeogenesis. It also lowers intestinal glucose absorption and enhances peripheral insulin sensitivity, resulting in lower fasting and post‑prandial blood glucose levels.

The appropriate dose of Metformin Al 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.

Safety of Metformin during pregnancy and lactation is not fully established. Healthcare providers should weigh potential benefits against possible risks and discuss them with the patient. If prescribed, close monitoring is recommended.

To order Metformin Al, 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 belongs to the biguanide class and is often first‑line therapy because it does not cause weight gain and has a low risk of hypoglycemia when used alone. Compared with sulfonylureas, it has a more favorable safety profile, while insulin provides stronger glucose reduction but requires injection.

Metformin Al should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original container, protect it from moisture, and avoid exposure to direct sunlight or extreme heat to maintain potency.

Metformin Al is taken orally, usually with meals to reduce gastrointestinal discomfort. The tablets are swallowed whole with a glass of water and should not be crushed, chewed, or dissolved 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 severe renal impairment, liver disease, or excessive alcohol intake. Prompt medical attention is required if symptoms such as rapid breathing, muscle pain, or abdominal discomfort develop.

Metformin 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 in those receiving iodinated contrast media without appropriate discontinuation. Clinicians should assess each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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