Product image of Metformin Teva (Metformin) supplied by GNH India

Metformin Teva

Active Ingredient:
Metformin
Origin:
EU

Metformin Teva (Metformin)

Metformin, the active ingredient in Metformin Teva, is a biguanide presented as an oral tablet for oral use. It reduces hepatic glucose production and increases peripheral insulin sensitivity, and is used to manage type 2 diabetes mellitus in adults.

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

Manufacturer / TM Owner

Teva B.V

1
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Indications & Clinical Uses

  • Metformin is a biguanide antidiabetic that improves glucose control in several metabolic conditions.
  • Type 2 diabetes mellitus: improves glycaemic control by lowering fasting and post‑prandial blood glucose.
  • Prediabetes (impaired glucose tolerance): helps delay progression to overt diabetes.
  • Polycystic ovary syndrome: reduces insulin resistance and may restore ovulatory function.

How It Works

  • Metformin acts primarily by inhibiting hepatic gluconeogenesis through activation of AMP‑activated protein kinase (AMPK). This reduces liver glucose output and enhances insulin‑mediated glucose uptake in muscle and adipose tissue, thereby improving peripheral insulin sensitivity and lowering circulating blood glucose levels.

Side Effects

Metformin is generally well tolerated, but a range of adverse reactions can occur.

Common Side Effects

  • Nausea
  • Diarrhoea
  • Abdominal discomfort
  • Metallic taste
  • Loss of appetite
  • Flatulence

Serious or Rare Side Effects

  • Lactic acidosis (potentially life‑threatening)
  • Severe skin reactions such as Stevens‑Johnson syndrome
  • Hepatic failure
  • Hypoglycaemia when combined with other antidiabetics
  • Vitamin B12 deficiency with long‑term use
  • Acute pancreatitis (rare)

Precautions & Warnings

Metformin should be used with attention to several safety considerations.

  • Renal function: assess creatinine clearance before initiation and periodically thereafter.
  • Hepatic function: avoid in patients with significant liver disease due to lactic acidosis risk.
  • Lactic acidosis: discontinue promptly if symptoms such as unexplained fatigue, dyspnoea, or abdominal pain develop.
  • Vitamin B12 monitoring: consider periodic assessment during long‑term therapy.
  • Pregnancy and lactation: use only if clearly needed after risk‑benefit evaluation.
  • Store at room temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

Metformin may interact with several medicines, requiring careful management.

Major Interactions (Avoid)

  • Iodinated contrast media: increase risk of lactic acidosis; suspend metformin before and after imaging.
  • Alcohol: potentiates lactic acidosis.
  • Cimetidine: may raise metformin plasma concentrations.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors and ARBs: may affect renal function, requiring dose adjustment.
  • Beta‑blockers: can mask hypoglycaemia symptoms.
  • Diuretics: may reduce renal clearance of metformin.
  • Corticosteroids: may increase blood glucose, necessitating tighter monitoring.
  • Warfarin: may alter INR, requiring regular coagulation checks.

Frequently Asked Questions

Metformin Teva is an oral antidiabetic medication indicated primarily for the management of type 2 diabetes mellitus. It helps lower elevated blood glucose levels by improving the body’s response to insulin and decreasing glucose production in the liver.

Metformin works by activating AMP‑activated protein kinase (AMPK), which suppresses hepatic gluconeogenesis and enhances peripheral glucose uptake. This dual action reduces the amount of glucose released into the bloodstream and improves insulin sensitivity in muscle and fat tissues.

The dosage of Metformin Teva is individualized by the prescribing healthcare professional based on the patient’s clinical condition, renal function, and response to therapy. The prescriber determines the appropriate strength, frequency, and titration schedule.

Metformin may be used during pregnancy or lactation only when the potential benefit justifies the potential risk to the fetus or infant. Healthcare providers evaluate each case carefully, and the drug should be prescribed by a qualified professional.

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 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, it does not cause weight gain and has a well‑established safety profile.

Store Metformin Teva at room temperature, below 25 °C, in the original packaging to protect it from moisture and heat. Keep the container tightly closed and out of reach of children.

Metformin Teva is taken orally, usually with meals to reduce gastrointestinal discomfort. The tablets should be swallowed whole with a 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 characterized by rapid breathing, muscle pain, and abdominal discomfort. Prompt medical attention is required if these symptoms occur, especially in patients with renal or hepatic impairment.

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 radiographic contrast studies without appropriate interruption of therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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