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

Metformina Cinfa

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformina Cinfa (Metformin Hydrochloride)

Metformin Hydrochloride, the active ingredient in Metformina Cinfa, is a biguanide presented as an oral tablet for oral use. It is used to improve blood glucose control in adults with type 2 diabetes and related glucose‑handling disorders.

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

Manufacturer / TM Owner

Laboratorios Cinfa S.A.

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Indications & Clinical Uses

Metformina Cinfa, a biguanide antidiabetic, acts on glucose metabolism to lower elevated blood sugar levels.

  • Type 2 diabetes mellitus: improves glycemic control and reduces HbA1c.
  • Prediabetes (impaired fasting glucose): delays progression to overt diabetes.
  • Gestational diabetes (when diet alone is insufficient): helps maintain maternal glucose within target ranges.

How It Works

  • Metformin Hydrochloride primarily inhibits hepatic gluconeogenesis, decreasing the liver's production of glucose. It also enhances peripheral insulin sensitivity by increasing glucose uptake in muscle and adipose tissue and modestly reduces intestinal glucose absorption, collectively lowering fasting and post‑prandial blood glucose concentrations.

Side Effects

Metformina Cinfa may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: loose stools, especially during treatment initiation.
  • Abdominal discomfort: cramping or bloating.
  • Metallic taste: transient alteration of taste perception.
  • Loss of appetite: reduced desire to eat.
  • Flatulence: increased gas production.

Serious or Rare Side Effects

  • Lactic acidosis: rare but potentially fatal metabolic disturbance.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Hypoglycemia: when combined with insulin or sulfonylureas.
  • Vitamin B12 deficiency: long‑term use may reduce B12 absorption.

Precautions & Warnings

Before initiating Metformina Cinfa, clinicians should evaluate patient‑specific risk factors and monitor relevant parameters.

  • Renal function: assess creatinine clearance and avoid use in severe renal impairment.
  • Hepatic function: evaluate liver enzymes; contraindicated in acute liver disease.
  • Risk of lactic acidosis: avoid in conditions predisposing to hypoxia or severe infection.
  • Concomitant medications: review drugs that may affect renal clearance or increase acidosis risk.
  • Gastrointestinal tolerance: advise patients to take with meals to reduce upset.
  • Store at room temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate acute renal failure and lactic acidosis.
  • Cimetidine: can increase metformin plasma concentrations.
  • Alcohol: potentiates risk of lactic acidosis.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycemia symptoms.
  • Diuretics: can affect renal function and metformin clearance.
  • ACE inhibitors/ARBs: monitor renal function and electrolytes.
  • NSAIDs: may reduce renal perfusion, increasing metformin levels.
  • Sulfonylureas: heightened risk of hypoglycemia when combined.

Frequently Asked Questions

Metformina Cinfa contains metformin hydrochloride, a biguanide oral antidiabetic used to lower elevated blood glucose in adults with type 2 diabetes, to improve glycemic control in prediabetes, and, in some cases, to assist management of gestational diabetes when diet alone is insufficient.

Metformin reduces hepatic glucose production by inhibiting gluconeogenesis, increases peripheral insulin sensitivity, and modestly decreases intestinal glucose absorption. These actions collectively lower fasting and post‑prandial blood glucose levels without directly stimulating insulin secretion.

The specific dosage and titration schedule for Metformina Cinfa are determined by the prescribing clinician based on the individual’s renal function, glycemic targets, and overall health status. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Metformina Cinfa is classified as pregnancy category unknown in many regions. It may be used during pregnancy when the potential benefit outweighs risk, such as in gestational diabetes, but this decision rests with the obstetrician. Metformin does pass into breast milk in small amounts; breastfeeding mothers should discuss continuation with their healthcare provider.

To request Metformina Cinfa, 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 (including any cold‑chain requirements) and necessary import documentation.

Metformina Cinfa (metformin) belongs to the biguanide class and is often first‑line therapy because it improves insulin sensitivity without causing weight gain. Compared with sulfonylureas, it has a lower risk of hypoglycemia, and unlike insulin, it is administered orally. Its efficacy is well‑established, and it is generally less expensive than newer agents such as GLP‑1 receptor agonists.

Metformina Cinfa should be stored at room temperature, below 25 °C, in the original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use if the tablet shows signs of damage or discoloration.

Metformina Cinfa is taken orally, usually with meals to reduce gastrointestinal upset. The tablets are swallowed whole with a full glass of water. Patients should not crush, chew, or split extended‑release formulations 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 severe renal or hepatic impairment, hypoxia, or excessive alcohol intake. Other serious risks include severe skin reactions such as Stevens‑Johnson syndrome and significant vitamin B12 deficiency with long‑term use.

Metformina Cinfa is contraindicated in patients with severe renal impairment (eGFR < 30 mL/min/1.73 m²), acute or chronic metabolic acidosis, including diabetic ketoacidosis, and known hypersensitivity to metformin or any component of the formulation. Caution is also advised for individuals with liver disease, heart failure, or a history of lactic acidosis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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