Product image of Metformina Dinerfene Laboratórios Azevedos – Indústria Farmacêutica (Metformin Hydrochloride) supplied by GNH India

Metformina Dinerfene Laboratórios Azevedos – Indústria Farmacêutica

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformina Dinerfene Laboratórios Azevedos – Indústria Farmacêutica (Metformin Hydrochloride)

Metformin Hydrochloride, the active ingredient in Metformina Dinerfene, is a biguanide presented as an oral tablet for oral use. It is used to improve glycemic control in adults with type 2 diabetes mellitus and is indicated for patients who require adjunctive therapy when diet and exercise alone are insufficient.

GNH India supplies Metformina Dinerfene as a licensed, GDP‑compliant international pharmaceutical product serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Laboratórios Azevedos - Indústria Farmacêutica, S.A.

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Indications & Clinical Uses

Metformin is indicated for the management of type 2 diabetes mellitus, a chronic metabolic disorder characterized by insulin resistance and elevated blood glucose levels, and is used as part of a comprehensive therapeutic regimen that includes diet, exercise and other antidiabetic agents.

  • Type 2 diabetes mellitus: improves blood glucose levels and reduces HbA1c when used as part of a comprehensive treatment plan.

How It Works

  • Metformin primarily inhibits hepatic gluconeogenesis by activating AMP‑activated protein kinase (AMPK), which reduces glucose production. It also enhances peripheral insulin sensitivity by increasing glucose uptake in muscle and adipose tissue and modestly decreases intestinal absorption of glucose, collectively contributing to lower plasma glucose concentrations.

Side Effects

Metformin is generally well tolerated, but several adverse reactions have been reported.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: frequent loose stools, especially during initiation.
  • Abdominal discomfort: cramping or bloating.
  • Metallic taste: transient alteration of taste perception.
  • Weight loss: modest reduction in body weight.
  • Vitamin B12 deficiency: decreased absorption with long‑term use.

Serious or Rare Side Effects

  • Lactic acidosis: rare but potentially fatal metabolic acidosis.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Hypoglycemia: usually when combined with other glucose‑lowering agents.
  • Anemia: due to reduced red blood cell production.
  • Electrolyte imbalance: especially with prolonged diarrhea.

Precautions & Warnings

Metformin should be used with careful clinical monitoring.

  • Renal function assessment: avoid or adjust dose in patients with impaired kidney function.
  • Hepatic function monitoring: use cautiously in liver disease.
  • Lactic acidosis risk: discontinue before radiologic contrast procedures.
  • Elderly patients: start at low dose and titrate slowly.
  • Heart failure: evaluate severity before initiation.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Metformin may interact with several medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Iodinated contrast agents: increase risk of lactic acidosis; withhold metformin before and after imaging.
  • Cimetidine: can raise metformin plasma concentrations.
  • Alcohol excess: potentiates lactic acidosis.
  • Rifampicin: may reduce metformin effectiveness.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycemia symptoms.
  • Diuretics: can affect renal clearance of metformin.
  • ACE inhibitors/ARBs: monitor renal function and electrolytes.
  • Other antidiabetic agents: risk of additive hypoglycemia.
  • Thyroid hormones: may alter glucose metabolism.

Frequently Asked Questions

Metformina Dinerfene contains metformin hydrochloride and is used to improve blood glucose control in adults with type 2 diabetes mellitus. It is prescribed as part of a comprehensive management plan that includes diet, exercise and, when needed, additional antidiabetic medications.

Metformin lowers blood sugar primarily by inhibiting hepatic glucose production through activation of AMP‑activated protein kinase (AMPK). It also increases insulin sensitivity in peripheral tissues, enhancing glucose uptake by muscle and fat cells, and modestly reduces intestinal glucose absorption.

The dose of Metformina Dinerfene 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 and any subsequent titration.

Metformin crosses the placenta and is classified as a pregnancy category that requires risk‑benefit assessment. It may be continued during pregnancy for women with gestational diabetes under specialist supervision. Metformin is excreted in breast milk; continuation while breastfeeding should be decided by the 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 the first‑line oral therapy for type 2 diabetes because of its efficacy, low risk of hypoglycemia and favorable impact on weight. Compared with sulfonylureas, it does not cause insulin release, and unlike newer agents such as GLP‑1 agonists, it is inexpensive and widely available.

Metformina Dinerfene tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and do not use after the expiry date.

Metformina Dinerfene is taken orally, usually with meals to reduce gastrointestinal discomfort. The tablets are swallowed whole with a glass of water. Patients should follow the dosing schedule prescribed by their 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, abdominal discomfort or unusual fatigue develop.

Metformina Dinerfene is contraindicated in patients with known hypersensitivity to metformin, severe renal impairment (eGFR < 30 mL/min/1.73 m²), acute or chronic metabolic acidosis, including diabetic ketoacidosis, and in those receiving radiographic contrast studies without appropriate discontinuation.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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