Product image of Metformin Hydrochloride Accord Healthcare (Metformin Hydrochloride) supplied by GNH India

Metformin Hydrochloride Accord Healthcare

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformin Hydrochloride Accord Healthcare (Metformin Hydrochloride)

Metformin Hydrochloride, the active ingredient in Metformin Hydrochloride Accord Healthcare, is a Biguanide presented as an oral tablet for oral use. It reduces hepatic glucose production and improves peripheral insulin sensitivity, thereby treating type 2 diabetes mellitus in adults.

GNH India supplies Metformin Hydrochloride Accord Healthcare as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing consistent quality and regulatory compliance for global distribution and supporting patient care across diverse markets. The product complies with European Union pharmacopeial standards and undergoes rigorous quality testing.

Manufacturer / TM Owner

Accord Healthcare Limited

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Indications & Clinical Uses

Metformin Hydrochloride is used in the management of type 2 diabetes mellitus, a disorder of glucose metabolism.

  • Type 2 diabetes mellitus: improves glycemic control by lowering fasting and post‑prandial blood glucose levels.
  • Prediabetes: reduces the risk of progression to overt diabetes through improved insulin sensitivity.
  • Polycystic ovary syndrome: helps ameliorate insulin resistance and may improve menstrual regularity.

How It Works

  • Metformin Hydrochloride acts primarily by inhibiting hepatic gluconeogenesis, thereby decreasing endogenous glucose production. It also enhances peripheral glucose uptake in muscle and adipose tissue by increasing insulin‑mediated signaling and improves insulin sensitivity. Additional actions include modest reduction of intestinal glucose absorption and favorable effects on lipid metabolism, contributing to its overall antidiabetic profile.

Side Effects

Metformin Hydrochloride may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Nausea: transient stomach upset, often mild.
  • Diarrhea: loose stools, usually early in therapy.
  • Abdominal discomfort: cramping or pain in the abdomen.
  • Metallic taste: temporary 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 life‑threatening accumulation of lactate.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatic dysfunction: signs of liver injury including jaundice.
  • Hypoglycemia: when combined with other glucose‑lowering agents.
  • Pancreatitis: inflammation of the pancreas.
  • Anemia: due to reduced red blood cell production.

Precautions & Warnings

Before initiating Metformin Hydrochloride, several precautionary measures should be considered to ensure safe use.

  • Renal function: assess creatinine clearance and avoid use in severe renal impairment.
  • Liver disease: use with caution and monitor hepatic enzymes.
  • Alcohol consumption: limit intake to reduce risk of lactic acidosis.
  • Concomitant medications: review for drugs that may affect renal function or increase metformin levels.
  • Pregnancy and lactation: discuss potential risks with the prescriber.
  • Store at ambient temperature: keep below 25 °C in the original packaging, protected from moisture and light.

Avoid Interactions

Metformin Hydrochloride can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate acute renal failure 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: can affect renal clearance of metformin.
  • ACE inhibitors or ARBs: require monitoring of renal function and electrolytes.

Frequently Asked Questions

Metformin Hydrochloride is prescribed primarily 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.

The drug works by inhibiting hepatic gluconeogenesis, which reduces the liver’s production of glucose. It also increases insulin‑mediated glucose uptake in muscle and fat tissue, enhancing overall insulin sensitivity and contributing to better blood‑sugar control.

The prescribed dose of Metformin Hydrochloride is individualized by the treating physician. Factors such as the patient’s renal function, age, glycemic targets, and response to therapy are considered when establishing the appropriate dosing regimen.

Safety data for Metformin Hydrochloride in pregnancy are limited, and the medication should only be used if the potential benefits outweigh the risks. During breastfeeding, it is excreted in small amounts in milk, so a prescriber should evaluate the need for continued therapy.

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 is a first‑line therapy for type 2 diabetes because of its efficacy, low risk of hypoglycemia and favorable impact on weight. Compared with sulfonylureas or insulin, it does not cause significant weight gain and has a well‑established safety profile, though it requires monitoring of renal function.

Metformin Hydrochloride tablets should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original container, protect it from moisture and direct sunlight, and ensure the packaging remains tightly closed until use.

The medication is taken orally, usually with meals to reduce gastrointestinal discomfort. Tablets are swallowed whole with a glass of water. The exact timing and frequency are determined by the prescribing clinician based on individual therapeutic goals.

The most serious adverse effect is lactic acidosis, a rare but potentially fatal condition characterized by elevated blood lactate levels. Early signs include unexplained fatigue, muscle pain, rapid breathing, and abdominal discomfort, and immediate medical attention is required if they occur.

Metformin is contraindicated in patients with severe renal impairment (eGFR < 30 mL/min/1.73 m²), known hypersensitivity to the drug, acute or chronic metabolic acidosis, and in those who have experienced lactic acidosis while on metformin therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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