Product image of Metformina + Sitagliptina Ratiopharm (Metformin Hydrochloride, Sitagliptin) supplied by GNH India

Metformina + Sitagliptina Ratiopharm

Active Ingredient:
Metformin Hydrochloride, Sitagliptin
Origin:
EU

Metformina + Sitagliptina Ratiopharm (Metformin Hydrochloride, Sitagliptin)

Metformin hydrochloride and sitagliptin, the active ingredient in Metformina + Sitagliptina Ratiopharm, is a biguanide and DPP‑4 inhibitor presented as an oral tablet formulation for oral use. It is indicated for the management of type 2 diabetes mellitus in adults.
GNH India supplies Metformina + Sitagliptina Ratiopharm as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Ratiopharm-Comercio E Industria De Produtos Farmaceuticos Lda

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Indications & Clinical Uses

Metformina + Sitagliptina Ratiopharm is used in the treatment of type 2 diabetes mellitus, acting on glucose metabolism pathways.

  • Type 2 diabetes mellitus: improves overall glycaemic control and reduces HbA1c levels.
  • Adjunct to diet and exercise in type 2 diabetes: provides additional glucose lowering when metformin alone is insufficient.
  • Combination therapy for metabolic control: enhances insulin secretion and peripheral insulin sensitivity, aiding long‑term disease management.

How It Works

  • Metformin reduces hepatic gluconeogenesis and increases peripheral insulin sensitivity, while sitagliptin inhibits the dipeptidyl peptidase‑4 enzyme, prolonging endogenous incretin activity. The combined effect results in decreased glucose production, enhanced insulin release in a glucose‑dependent manner, and improved overall glycaemic regulation.

Side Effects

Common Side Effects

  • Gastrointestinal upset: nausea, abdominal discomfort, or diarrhea.
  • Headache: mild to moderate intensity.
  • Upper respiratory symptoms: nasopharyngitis or mild cough.
  • Dizziness: transient light‑headedness.
  • Fatigue: general tiredness.

Serious or Rare Side Effects

  • Lactic acidosis: rare but potentially fatal metabolic disturbance.
  • Severe hypoglycaemia: especially when combined with insulin secretagogues.
  • Pancreatitis: acute inflammation of the pancreas.
  • Severe allergic reactions: rash, angioedema, or anaphylaxis.
  • Hepatic failure: marked liver enzyme elevation or dysfunction.

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor appropriately.

  • Renal function: assess creatinine clearance; adjust or avoid in severe impairment.
  • Hepatic disease: use with caution; monitor liver enzymes.
  • Risk of lactic acidosis: avoid in conditions predisposing to hypoxia.
  • Elderly patients: start at lower dose and monitor for adverse events.
  • Alcohol consumption: limit intake to reduce lactic acidosis risk.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Metformina + Sitagliptina Ratiopharm may interact with several drug classes.

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate renal dysfunction when combined with metformin.
  • Insulin secretagogues (e.g., sulfonylureas): increase risk of severe hypoglycaemia.
  • Strong CYP2C8 inhibitors: may elevate sitagliptin plasma levels.

Moderate Interactions (Monitor Closely)

  • Diuretics: can affect renal clearance of metformin.
  • ACE inhibitors or ARBs: may enhance renal effects of metformin.
  • Warfarin: monitor INR as sitagliptin may alter anticoagulant effect.

Frequently Asked Questions

Metformina + Sitagliptina Ratiopharm is prescribed for adults with type 2 diabetes mellitus to improve blood glucose control. It combines metformin, which lowers hepatic glucose output, with sitagliptin, which enhances insulin secretion in response to meals, providing a complementary approach to glycaemic management.

Metformin works by decreasing hepatic glucose production and increasing peripheral insulin sensitivity. Sitagliptin inhibits the enzyme dipeptidyl peptidase‑4, prolonging the action of incretin hormones that stimulate insulin release and suppress glucagon secretion in a glucose‑dependent manner. Together they target two distinct pathways to lower blood sugar.

The specific dose and dosing schedule are determined by the prescribing healthcare professional based on individual patient factors such as renal function, glycaemic targets, and concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose without medical guidance.

Safety data for the combination in pregnancy are limited, and it is generally recommended to avoid use unless the potential benefit justifies the risk. Metformin may be used in certain pregnancy situations, but sitagliptin lacks sufficient data. Breastfeeding mothers should consult their physician, as the drug may be excreted in milk.

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 (including any cold‑chain requirements), and necessary import documentation.

Compared with metformin monotherapy, the addition of sitagliptin offers greater HbA1c reduction without the weight gain associated with some other agents like sulfonylureas. Unlike insulin, it does not cause hypoglycaemia when used alone, and it provides a convenient oral fixed‑dose option versus injectable GLP‑1 receptor agonists.

Store the tablets at temperatures below 25 °C in their original packaging, protecting them from moisture and direct sunlight. Keep the container tightly closed and out of reach of children. Do not use the product after the expiry date printed on the label.

The medication is taken orally, usually with meals to reduce gastrointestinal discomfort. Tablets should be swallowed whole with a full glass of water. Patients should follow the dosing schedule prescribed by their healthcare provider and maintain consistent timing each day.

Serious risks include lactic acidosis, a rare but potentially fatal condition linked to metformin, especially in patients with renal impairment or severe hypoxia. Additionally, sitagliptin has been associated with pancreatitis and severe hypersensitivity reactions. Prompt medical attention is required if symptoms such as unexplained muscle pain, abdominal pain, or rash develop.

Patients with severe renal impairment (eGFR < 30 mL/min/1.73 m²), known hypersensitivity to metformin, sitagliptin, or any excipients, and those with a history of lactic acidosis should avoid this medication. It is also contraindicated in individuals with acute or chronic metabolic acidosis, including diabetic ketoacidosis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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