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

Metformin Terapia

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformin Terapia (Metformin Hydrochloride)

Metformin, the active ingredient in Metformin Terapia, is a biguanide presented as an oral tablet for oral use. It is prescribed to improve blood glucose control in adults with type 2 diabetes mellitus and related insulin‑resistant conditions.
GNH India supplies Metformin Terapia as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Terapia S.A.

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Indications & Clinical Uses

Metformin Terapia belongs to the biguanide class and is used to manage disorders of glucose metabolism.

  • Type 2 diabetes mellitus: lowers fasting and post‑prandial blood glucose levels.
  • Prediabetes (impaired glucose tolerance): helps delay progression to overt diabetes.
  • Polycystic ovary syndrome: improves insulin sensitivity and may regularise menstrual cycles.

How It Works

  • Metformin reduces hepatic gluconeogenesis and increases peripheral glucose uptake by activating AMP‑activated protein kinase (AMPK). This leads to decreased liver glucose output and enhanced insulin‑mediated glucose utilization in muscle and adipose tissue, thereby improving overall glycaemic control without directly stimulating insulin secretion.

Side Effects

Metformin Terapia 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 in taste perception.
  • Loss of appetite: reduced desire to eat.
  • Vitamin B12 deficiency: possible decrease with long‑term use.

Serious or Rare Side Effects

  • Lactic acidosis: a rare but life‑threatening buildup of lactic acid.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatic dysfunction: abnormal liver enzymes or hepatitis.
  • Hypoglycaemia: when combined with other glucose‑lowering agents.
  • Acute pancreatitis: inflammation of the pancreas.

Precautions & Warnings

Before prescribing Metformin Terapia, clinicians should consider several safety factors.

  • Renal function: avoid or adjust dose in patients with impaired kidney function.
  • Hepatic disease: use with caution in those with liver impairment.
  • Cardiovascular status: monitor in patients with unstable heart failure.
  • Alcohol intake: limit consumption to reduce risk of lactic acidosis.
  • Pregnancy and lactation: assess risk‑benefit, as safety data are limited.
  • Store at ambient temperature: keep below 25°C in the original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycaemia symptoms.
  • Diuretics (thiazides): can affect renal clearance of metformin.
  • ACE inhibitors or ARBs: monitor renal function and electrolytes.
  • Alcohol: potentiates risk of lactic acidosis.

Frequently Asked Questions

Metformin Terapia is an oral antidiabetic medication indicated for the management of type 2 diabetes mellitus. It improves blood glucose control by decreasing hepatic glucose production and increasing peripheral insulin sensitivity.

Metformin activates AMP‑activated protein kinase (AMPK), which suppresses liver gluconeogenesis and enhances glucose uptake in muscle and fat cells. This dual action lowers fasting and post‑prandial blood glucose without stimulating insulin secretion.

The dose of Metformin Terapia is individualized by the prescribing healthcare professional based on the patient’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 data for Metformin in pregnancy and lactation are limited. The drug should only be used when the potential benefit outweighs the potential risk, and the decision must be made by a qualified healthcare provider.

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 belongs to the biguanide class and is often preferred as first‑line therapy because it does not cause weight gain and has a low risk of hypoglycaemia compared with sulfonylureas or insulin. Its mechanism differs from thiazolidinediones, which act on PPAR‑γ receptors.

Metformin Terapia should be stored at ambient temperature, below 25 °C, in the original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain its stability.

Metformin Terapia is taken orally, usually with meals to reduce gastrointestinal discomfort. Tablets should be swallowed whole with a full glass of water and not 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 severe renal impairment, hepatic 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, and those with known hypersensitivity to metformin or other biguanides.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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