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

Metformina Teva Italia

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformina Teva Italia (Metformin Hydrochloride)

Metformin, the active ingredient in Metformina Teva Italia, is a Biguanide presented as a tablet for oral use. It is indicated for the management of type 2 diabetes mellitus in adult patients. The drug improves glycemic control by decreasing hepatic glucose production and enhancing peripheral insulin sensitivity.

GNH India supplies Metformina Teva Italia as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with capabilities for bulk manufacturing, quality assurance and regulatory support.

Manufacturer / TM Owner

Teva Italia S.R.L.

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Indications & Clinical Uses

  • Metformina Teva Italia (metformin) is used in the management of disorders related to glucose metabolism.
  • Type 2 diabetes mellitus: lowers blood glucose levels and improves overall glycemic control.
  • Prediabetes (impaired glucose tolerance): helps delay progression to overt diabetes.
  • Polycystic ovary syndrome: reduces insulin resistance and may improve ovulatory function.

How It Works

  • Metformin inhibits mitochondrial respiratory‑chain complex I, leading to reduced hepatic gluconeogenesis. The consequent decline in hepatic glucose output, together with enhanced peripheral glucose uptake and improved insulin receptor signaling, lowers plasma glucose concentrations. Additional actions include modest reduction of intestinal glucose absorption and modulation of gut microbiota, which together contribute to its antidiabetic effect.

Side Effects

Metformina Teva Italia may be associated with a range of adverse reactions, classified by frequency.

Common Side Effects

  • Nausea: feeling of sickness often occurring early in therapy.
  • Diarrhea: loose stools that may be transient.
  • Metallic taste: temporary alteration in taste perception.
  • Abdominal discomfort: mild stomach pain or cramping.

Serious or Rare Side Effects

  • Lactic acidosis: rare but potentially fatal accumulation of lactate.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Vitamin B12 deficiency: may develop with long‑term use.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.

Precautions & Warnings

  • When prescribing Metformina Teva Italia, clinicians should consider several safety measures.
  • Renal function: assess eGFR before initiating and monitor periodically.
  • Liver disease: use with caution in patients with hepatic impairment.
  • Alcohol consumption: avoid excessive intake to reduce lactic acidosis risk.
  • Risk of lactic acidosis: discontinue if patient develops severe hypoxia, sepsis or organ failure.
  • Pregnancy and lactation: evaluate risk‑benefit and consider alternative therapy.
  • Store at room temperature: keep in original container, protect from moisture and heat.

Avoid Interactions

Metformina Teva Italia can interact with other medicines; some combinations should be avoided while others require monitoring.

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate renal impairment and increase lactic acidosis risk.
  • Cimetidine: can raise metformin plasma concentrations.
  • Alcohol: excessive intake heightens lactic acidosis potential.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask symptoms of hypoglycemia.
  • Diuretics (especially thiazides): affect renal clearance of metformin.
  • ACE inhibitors or ARBs: monitor renal function and electrolytes.

Frequently Asked Questions

Metformina Teva Italia contains metformin, which is prescribed to lower blood glucose in adults with type 2 diabetes mellitus. It helps achieve better glycemic control by reducing the amount of glucose produced by the liver and by improving the body's response to insulin.

Metformin works mainly by inhibiting mitochondrial complex I, which suppresses hepatic gluconeogenesis. The drug also increases peripheral glucose uptake and improves insulin signaling, leading to lower circulating glucose levels. Additional effects on intestinal glucose absorption and gut microbiota contribute to its overall antidiabetic activity.

The dose of metformin is individualized by the prescribing clinician based on the patient’s clinical condition, renal function and response to therapy. The prescriber determines the appropriate starting dose, titration schedule and maximum daily amount, following local prescribing guidelines.

Safety data for metformin in pregnancy are limited, and the drug is classified as pregnancy category unknown. Clinicians must weigh potential benefits against possible risks and consider alternative treatments when appropriate. Metformin is excreted in breast milk, so breastfeeding mothers should discuss continuation with their 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 generally preferred as first‑line therapy because it does not cause hypoglycaemia when used alone and may aid modest weight loss. In contrast, sulfonylureas stimulate insulin release and carry a higher risk of hypoglycaemia and weight gain.

Metformina Teva Italia should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and avoid storing it in humid or excessively hot environments.

The medication is taken orally, usually with meals to minimise gastrointestinal discomfort. Tablets should be swallowed whole with a glass of water; they are not intended for crushing, chewing or splitting unless specifically advised by a healthcare professional.

The most serious adverse events are lactic acidosis, a rare but life‑threatening condition, and severe skin reactions such as Stevens‑Johnson syndrome. Early signs of lactic acidosis include unexplained fatigue, muscle pain, abdominal discomfort, rapid breathing or a feeling of coldness. Prompt medical attention is essential if these symptoms appear.

Metformina Teva Italia is contraindicated in patients with severe renal impairment (eGFR < 30 mL/min/1.73 m²), known hypersensitivity to metformin, acute or chronic metabolic acidosis, and those receiving radiographic contrast studies that may affect kidney function. Clinicians should also avoid use in individuals with uncontrolled heart failure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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