Product image of Metformina Hexal Ag (Metformin Hydrochloride) supplied by GNH India

Metformina Hexal Ag

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformina Hexal Ag (Metformin Hydrochloride)

Metformin, the active ingredient in Metformina Hexal Ag, is a Biguanide presented as a tablet for oral use. It treats type 2 diabetes mellitus in adults.
GNH India supplies Metformina Hexal Ag as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Hexal Ag

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Indications & Clinical Uses

Metformina Hexal Ag is used to manage disorders of glucose metabolism, primarily in the type 2 diabetes pathway.

  • Type 2 diabetes mellitus: improves glycaemic control and reduces fasting plasma glucose.
  • Impaired glucose tolerance: helps delay progression to overt diabetes.
  • Metabolic syndrome: assists in improving insulin sensitivity and modest weight management.

How It Works

  • Metformin reduces hepatic gluconeogenesis and increases peripheral glucose uptake by activating AMP‑activated protein kinase (AMPK). This leads to decreased hepatic glucose output, enhanced insulin‑mediated glucose utilization in muscle and adipose tissue, and modest reductions in intestinal glucose absorption, collectively improving overall glycaemic control.

Side Effects

Metformina Hexal Ag 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.
  • Vomiting: occasional emesis, usually early on.

Serious or Rare Side Effects

  • Lactic acidosis: rare but life‑threatening metabolic disturbance.
  • Severe hypoglycaemia: when combined with other glucose‑lowering agents.
  • Vitamin B12 deficiency: may develop with long‑term use.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Skin rash or hypersensitivity: including Stevens‑Johnson syndrome.
  • Allergic reactions: anaphylaxis or angioedema.

Precautions & Warnings

Before initiating Metformina Hexal Ag, several safety considerations should be reviewed.

  • Renal function: assess creatinine clearance; avoid in severe renal impairment.
  • Hepatic function: monitor liver enzymes; use cautiously in hepatic disease.
  • Monitor blood glucose: adjust dose based on glycaemic response.
  • Alcohol intake: limit consumption to reduce lactic acidosis risk.
  • Elderly patients: start with lower dose and titrate slowly.
  • Store at room temperature: keep in the original pack, protect from moisture and heat.

Avoid Interactions

Metformina Hexal Ag can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Iodinated contrast agents: increase risk of renal dysfunction and lactic acidosis.
  • Cimetidine: may raise metformin plasma concentrations.
  • Alcohol: potentiates lactic acidosis risk.
  • Diuretics (loop or thiazide): can impair renal clearance of metformin.
  • Nifedipine: may enhance metformin’s glucose‑lowering effect.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycaemia symptoms.
  • ACE inhibitors/ARBs: monitor renal function and electrolytes.
  • Other antidiabetic agents: risk of additive hypoglycaemia.
  • Thyroid hormones: may affect metabolic rate and glucose control.
  • Corticosteroids: can increase blood glucose, requiring dose adjustments.

Frequently Asked Questions

Metformina Hexal Ag contains metformin, a Biguanide indicated for the treatment of type 2 diabetes mellitus. It helps lower blood glucose by reducing liver glucose production and improving insulin sensitivity in peripheral tissues.

Metformin activates AMP‑activated protein kinase (AMPK), which suppresses hepatic gluconeogenesis, enhances glucose uptake in muscle, and reduces intestinal glucose absorption. These actions collectively improve glycaemic control without directly stimulating insulin secretion.

The exact dose of Metformina Hexal Ag is determined by the prescribing clinician based on the patient’s clinical condition, renal function, and response to therapy. Dosage adjustments are made during treatment to achieve optimal blood‑glucose targets.

Safety of metformin in pregnancy or lactation should be evaluated by a healthcare professional. While metformin is sometimes used in gestational diabetes, its use is decided case‑by‑case, and benefits must outweigh potential risks.

To 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 the first‑line oral therapy for type 2 diabetes due to 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 well‑established safety profile when renal function is adequate.

Metformina Hexal Ag should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight and excessive heat to maintain tablet integrity.

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

The most serious adverse reaction is lactic acidosis, a rare but potentially fatal condition, especially in patients with severe renal or hepatic impairment. Other serious concerns include severe hypoglycaemia when combined with insulin or sulfonylureas, and vitamin B12 deficiency with long‑term use.

Metformina Hexal Ag 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 with conditions predisposing to lactic acidosis such as severe liver disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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