Product image of Metformina + Pioglitazona Pentafarma (Metformin Hydrochloride, Pioglitazone) supplied by GNH India

Metformina + Pioglitazona Pentafarma

Active Ingredient:
Metformin Hydrochloride, Pioglitazone
Origin:
EU

Metformina + Pioglitazona Pentafarma (Metformin Hydrochloride, Pioglitazone)

Metformin Hydrochloride, the active ingredient in Metformina + Pioglitona Pentafarma, is a biguanide presented as an oral tablet for oral use. It is combined with pioglitazone, a thiazolidinedione, to treat type 2 diabetes mellitus in adult patients who require additional glycemic control.

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

Manufacturer / TM Owner

Pentafarma - Sociedade Tecnico-Medicinal S.A.

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Indications & Clinical Uses

Metformina + Pioglitona Pentafarma is used in the management of type 2 diabetes mellitus and related hyperglycaemic conditions.

  • Type 2 diabetes mellitus: improves overall glycaemic control when monotherapy is insufficient.
  • Elevated fasting plasma glucose: lowers fasting glucose levels.
  • High HbA1c: reduces HbA1c percentages toward target values.
  • Insulin resistance: enhances peripheral insulin sensitivity.
  • Hyperglycaemia after meals: attenuates post‑prandial glucose excursions.

How It Works

  • Metformin reduces hepatic gluconeogenesis and increases peripheral glucose uptake by activating AMP‑activated protein kinase, while pioglitazone binds to peroxisome proliferator‑activated receptor‑γ (PPAR‑γ) receptors, promoting transcription of insulin‑sensitive genes and improving adipocyte function. The combined actions decrease hepatic glucose output and enhance insulin sensitivity in muscle and adipose tissue, resulting in better overall blood‑sugar regulation.

Side Effects

The combination may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal discomfort.
  • Diarrhoea: frequent loose stools, especially at treatment initiation.
  • Weight gain: modest increase due to fluid retention or adipose tissue changes.
  • Edema: peripheral swelling, often in the ankles.
  • Headache: transient cranial discomfort.

Serious or Rare Side Effects

  • Lactic acidosis: a rare but life‑threatening metabolic disturbance.
  • Heart failure exacerbation: fluid overload leading to dyspnoea.
  • Hepatotoxicity: elevated liver enzymes indicating liver injury.
  • Bone fracture: increased risk of osteoporotic fractures.
  • Bladder cancer: potential association with long‑term pioglitazone use.

Precautions & Warnings

Patients should be evaluated for specific risk factors before initiating therapy.

  • Renal function: assess creatinine clearance and adjust if impaired.
  • Hepatic function: monitor liver enzymes prior to and during treatment.
  • Cardiac status: evaluate for existing heart failure before use.
  • Pregnancy and lactation: avoid unless benefits outweigh potential risks.
  • Concomitant medications: review for drugs that may affect glucose or renal function.
  • Store at room temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

Metformina + Pioglitona Pentafarma can interact with several medicines, requiring careful management.

Major Interactions (Avoid)

  • Insulin or sulfonylureas: increased risk of severe hypoglycaemia.
  • Cimetidine: may raise metformin plasma concentrations.
  • Strong CYP2C8 inhibitors (e.g., gemfibrozil): elevate pioglitazone levels.

Moderate Interactions (Monitor Closely)

  • Diuretics: may potentiate fluid retention and edema.
  • ACE inhibitors or ARBs: monitor renal function and potassium.
  • Contrast media: temporary suspension of metformin recommended to avoid renal complications.

Frequently Asked Questions

Metformina + Pioglitona Pentafarma is a fixed‑dose oral tablet that combines metformin and pioglitazone to improve blood‑sugar control in adults with type 2 diabetes mellitus, especially when a single agent does not achieve target glycaemic levels.

Metformin primarily lowers hepatic glucose production and increases peripheral glucose uptake via AMP‑activated protein kinase activation. Pioglitazone activates PPAR‑γ receptors, enhancing insulin sensitivity in muscle and adipose tissue. Together they address both excess glucose output and insulin resistance.

The appropriate dose is determined by the prescribing clinician based on individual patient factors such as renal function, glycaemic targets, and tolerability. Patients should follow the dosage instructions provided by their healthcare professional.

The safety of this combination in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and under close medical supervision.

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.

Compared with metformin alone, the addition of pioglitazone offers greater improvement in insulin sensitivity and can lower HbA1c further. Unlike sulfonylureas, it carries a lower risk of hypoglycaemia but may cause weight gain and fluid retention, which should be weighed against patient‑specific factors.

Store the tablets at room temperature, below 25 °C, in the original blister pack or bottle. Keep them away from moisture, direct sunlight and excessive heat to maintain product stability.

The medication is taken orally, usually with meals to reduce gastrointestinal discomfort. Tablets should be swallowed whole with a full glass of water and not crushed or chewed unless specifically instructed by a healthcare provider.

Serious risks include lactic acidosis (particularly in patients with renal impairment), worsening heart failure due to fluid retention, hepatotoxicity, and a possible increased risk of bladder cancer with long‑term pioglitazone use. Patients should be monitored regularly for these conditions.

The combination is contraindicated in patients with severe renal impairment, active liver disease, known hypersensitivity to either component, or a history of heart failure exacerbation. It should also be avoided in individuals with a prior diagnosis of bladder cancer.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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