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

Metformina Placasod

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformina Placasod (Metformin Hydrochloride)

Metformin, the active ingredient in Metformina Placasod, is a biguanide presented as an oral dosage form for oral use. It is indicated for the management of type 2 diabetes mellitus in adult patients, where it helps to lower elevated blood glucose levels by improving insulin sensitivity and reducing hepatic glucose output.

GNH India supplies Metformina Placasod as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation to support safe import and distribution across global markets.

Manufacturer / TM Owner

Sandoz Farmacéutica, S.A.

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Indications & Clinical Uses

Metformina Placasod is a biguanide antidiabetic that acts on glucose metabolism pathways.

  • Type 2 diabetes mellitus: improves overall glycemic control in adult patients.
  • Adjunct to diet and exercise in type 2 diabetes: lowers fasting plasma glucose when lifestyle measures alone are insufficient.
  • Prevention of progression from impaired glucose tolerance to type 2 diabetes: delays onset in high‑risk adults.

How It Works

  • Metformin primarily inhibits hepatic gluconeogenesis, reducing the liver's production of glucose. It also enhances peripheral insulin sensitivity by increasing glucose uptake in muscle tissue and decreasing intestinal absorption of glucose, thereby contributing to lower blood glucose concentrations without stimulating insulin secretion.

Side Effects

Metformina Placasod may cause a range of adverse reactions, most of which are related to the gastrointestinal system or metabolic disturbances.

Common Side Effects

  • Nausea: mild to moderate discomfort in the stomach.
  • Diarrhea: frequent loose stools, often transient.
  • Abdominal discomfort: cramping or pain in the abdomen.
  • Metallic taste: a persistent metallic sensation in the mouth.
  • Loss of appetite: reduced desire to eat.
  • Weight loss: modest reduction in body weight.

Serious or Rare Side Effects

  • Lactic acidosis: a rare but life‑threatening buildup of lactic acid.
  • Severe hypoglycemia: especially when combined with other antidiabetic agents.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Allergic reactions: rash, itching, or swelling.
  • Vitamin B12 deficiency: long‑term therapy may reduce absorption.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient-specific factors and monitor for potential complications.

  • Renal function: assess creatinine clearance and avoid use in severe renal impairment.
  • Hepatic function: evaluate liver enzymes, as dysfunction may increase risk of lactic acidosis.
  • Age considerations: start at lower doses in elderly patients and monitor tolerance.
  • Alcohol intake: advise patients to limit alcohol, which can potentiate lactic acidosis.
  • Concomitant medications: review for drugs that may affect renal function or increase metformin levels.
  • Store at ambient temperature: keep below 25°C in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Metformina Placasod can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Alcohol: enhances risk of lactic acidosis.
  • Diuretics: may affect renal clearance of metformin.
  • Corticosteroids: can raise blood glucose, requiring dose adjustments.
  • Beta‑blockers: may mask hypoglycemia symptoms.
  • Other antidiabetic agents (e.g., sulfonylureas): increase likelihood of hypoglycemia.

Frequently Asked Questions

Metformina Placasod contains metformin hydrochloride and is prescribed for the treatment of type 2 diabetes mellitus. It helps lower elevated blood glucose levels by improving the body's response to insulin and decreasing the amount of glucose produced by the liver.

Metformin acts primarily by inhibiting hepatic gluconeogenesis, which reduces the liver's output of glucose. It also enhances peripheral insulin sensitivity, promoting greater glucose uptake by muscle cells and decreasing intestinal glucose absorption, leading to overall better glycemic control.

The dosage of Metformina Placasod is individualized by the prescribing healthcare professional based on the patient’s clinical condition, renal function, and response to therapy. Patients should follow the exact dosing instructions provided by their prescriber and not adjust the dose on their own.

The safety of metformin during pregnancy and lactation is not fully established, and the pregnancy category for this product is listed as unknown. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential risks and benefits with their physician before using Metformina Placasod.

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.

Metformina Placasod (metformin) belongs to the biguanide class, which differs from sulfonylureas, insulin, and newer agents like GLP‑1 receptor agonists. Unlike sulfonylureas, metformin does not stimulate insulin secretion, reducing the risk of hypoglycemia, and it also promotes modest weight loss, making it a first‑line option for many patients.

Metformina Placasod should be stored at ambient temperature, preferably below 25 °C, in its original packaging to protect it from moisture and direct sunlight. Keep the product out of reach of children and do not use it after the expiration date printed on the label.

Metformina Placasod is taken orally, usually with meals to reduce gastrointestinal discomfort. The 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 adverse reaction is lactic acidosis, a rare but potentially fatal condition that can occur in patients with significant renal or hepatic impairment. Severe hypoglycemia may also develop when metformin is combined with other glucose‑lowering agents. Prompt medical attention is required if symptoms such as rapid breathing, muscle pain, or unusual fatigue appear.

Metformina Placasod 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 radiographic contrast studies that may affect kidney function. Clinicians should evaluate each patient’s medical history before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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