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

Metformina Teva

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformina Teva (Metformin Hydrochloride)

Metformin, the active ingredient in Metformina Teva, is a Biguanide presented as a tablet for oral use. It lowers elevated blood glucose by improving insulin sensitivity and decreasing hepatic glucose output, and is indicated for the management of type 2 diabetes mellitus in adult patients.

GNH India supplies Metformina Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, and clinics worldwide, with established logistics and quality assurance processes to ensure consistent product availability across markets for regulatory compliance.

Manufacturer / TM Owner

Teva Italia S.R.L.

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Indications & Clinical Uses

Metformin is an oral antidiabetic agent used in the management of type 2 diabetes mellitus.

  • Type 2 diabetes mellitus: improves glycemic control by lowering fasting and post‑prandial glucose levels.
  • Prediabetes (impaired fasting glucose or impaired glucose tolerance): helps delay progression to overt diabetes when combined with lifestyle measures.
  • Polycystic ovary syndrome (off‑label): may improve insulin resistance and restore ovulatory function.

How It Works

  • Metformin primarily inhibits hepatic gluconeogenesis by activating AMP‑activated protein kinase (AMPK), which reduces glucose production. It also enhances peripheral glucose uptake in muscle and adipose tissue by increasing insulin‑mediated glucose transport, and modestly lowers intestinal absorption of glucose, collectively improving overall insulin sensitivity.

Side Effects

Metformin is associated with a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Gastrointestinal upset: nausea, abdominal discomfort, and loss of appetite.
  • Diarrhea: frequent loose stools, especially during treatment initiation.
  • Metallic taste: transient alteration of taste perception.
  • Weight loss: modest reduction in body weight.
  • Vitamin B12 deficiency: decreased absorption with long‑term use.
  • Skin rash: mild erythema or pruritus.

Serious or Rare Side Effects

  • Lactic acidosis: rare but potentially fatal metabolic disturbance.
  • Severe hypoglycemia: when combined with insulin or sulfonylureas.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Pancreatitis: inflammation of the pancreas.
  • Anaphylactic reaction: rare systemic allergic response.
  • Blood dyscrasias: neutropenia or agranulocytosis.

Precautions & Warnings

Metformin requires careful monitoring and patient education to minimize risks.

  • Renal function assessment: evaluate creatinine clearance before initiation and periodically.
  • Lactic acidosis risk: avoid in patients with severe renal or hepatic impairment.
  • Alcohol consumption: limit intake to reduce lactic acidosis potential.
  • Elderly patients: start with lower doses and monitor tolerance.
  • Heart failure: assess stability before prescribing.
  • Store at room temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Iodinated contrast agents: can precipitate acute renal failure and increase lactic acidosis risk.
  • Cimetidine: may raise metformin plasma concentrations.
  • Alcohol: potentiates lactic acidosis.
  • Nitrates: combined use may increase risk of hypotension.
  • High‑dose vitamin B12 supplements: may interfere with absorption.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycemia symptoms.
  • Thiazide diuretics: can raise blood glucose levels.
  • ACE inhibitors: monitor renal function.
  • Corticosteroids: may reduce glycemic control.
  • Oral contraceptives: may affect metformin metabolism.

Frequently Asked Questions

Metformina Teva contains metformin, which is prescribed to improve blood glucose control in adults with type 2 diabetes mellitus. It works by decreasing liver glucose production and enhancing insulin sensitivity in peripheral tissues.

Metformin activates AMP‑activated protein kinase (AMPK), leading to reduced hepatic gluconeogenesis, increased glucose uptake by muscle, and decreased intestinal glucose absorption. These actions collectively lower blood sugar levels without stimulating insulin release.

The exact dose of Metformina Teva is determined by the prescribing clinician based on the patient’s medical condition, renal function, and response to therapy. Dosage adjustments are made individually and should follow the prescriber’s instructions.

Metformin crosses the placenta and is classified as a pregnancy‑category drug only when benefits outweigh risks. It is excreted in breast milk in small amounts. Decisions about use in pregnancy or lactation should be made by a healthcare professional after evaluating potential risks and benefits.

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.

Metformina Teva belongs to the biguanide class, which differs from sulfonylureas, DPP‑4 inhibitors, or SGLT2 inhibitors. It does not stimulate insulin secretion, carries a low risk of hypoglycemia when used alone, and may aid modest weight loss, making it a first‑line option for many patients.

Store Metformina Teva at room temperature, below 25 °C, in the original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain its stability and potency.

Metformina Teva is taken orally, usually with meals to reduce gastrointestinal discomfort. The tablet should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed by a healthcare provider.

The most serious risk is lactic acidosis, a rare but potentially fatal condition that can occur in patients with severe renal or hepatic impairment, excessive alcohol intake, or acute medical illness. Prompt medical attention is required if symptoms such as rapid breathing, muscle pain, or abdominal discomfort develop.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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