Product image of Gluvedus (Metformin Hydrochloride, Vildagliptin) supplied by GNH India

Gluvedus

Active Ingredient:
Metformin Hydrochloride, Vildagliptin
Origin:
EU

Gluvedus (Metformin Hydrochloride, Vildagliptin)

Gluvedus is a prescription oral medication that combines Metformin Hydrochloride and Vildagliptin. It is formulated as a tablet (strength not specified) and is marketed in the European Union. The product belongs to the biguanide and DPP‑4 inhibitor combination class and is used to improve blood glucose control in adults with type 2 diabetes mellitus.

Manufacturer / TM Owner

Verisfield S.M.S.A

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Indications & Clinical Uses

Gluvedus is indicated for the management of type 2 diabetes mellitus, typically when diet, exercise, and monotherapy are insufficient. It may be prescribed as part of a comprehensive treatment plan that includes lifestyle modifications.

  • Adjunct to diet and exercise in adults with type 2 diabetes.
  • Combination therapy when metformin alone does not achieve glycemic targets.
  • Used in patients requiring both insulin sensitization and incretin‑based effects.
  • May be considered when a single‑pill regimen is preferred for adherence.
  • Often prescribed alongside other antihyperglycemic agents as needed.

Side Effects

Side effects of Gluvedus vary in frequency and severity. Common reactions are usually mild and transient, while serious events are less frequent but require medical attention.

Common

  • Nausea or upset stomach
  • Diarrhea or loose stools
  • Headache
  • Upper respiratory tract infection symptoms
  • Mild hypoglycemia (especially with concomitant sulfonylureas)

Serious

  • Lactic acidosis (rare, associated with metformin)
  • Severe hypoglycemia
  • Pancreatitis
  • Severe allergic reactions such as rash or angioedema
  • Hepatic dysfunction

Precautions & Warnings

Before starting Gluvedus, certain health considerations should be reviewed. Patients and clinicians should be aware of the following precautions:

  • Assess renal function; avoid use in severe renal impairment.
  • Monitor liver enzymes periodically, especially in patients with hepatic disease.
  • Evaluate risk of lactic acidosis, particularly in conditions that predispose to hypoxia.
  • Use caution in elderly patients due to increased susceptibility to adverse effects.
  • Discontinue before any radiographic studies involving iodinated contrast agents.
  • Counsel women of childbearing potential about unknown pregnancy safety.

Avoid Interactions

Gluvedus can interact with several drug classes, influencing its efficacy or safety profile. Interactions are grouped by the level of risk.

Avoid

  • Iodinated contrast media (risk of renal impairment and lactic acidosis).
  • Strong CYP2C9 inhibitors that may increase vildagliptin levels.
  • Alcohol excess, which can potentiate metformin‑related lactic acidosis.

Use with caution

  • Sulfonylureas or insulin (increased risk of hypoglycemia).
  • Diuretics that affect renal function.
  • Corticosteroids, which may raise blood glucose levels.
  • Other antihyperglycemic agents, requiring dose adjustments.

Frequently Asked Questions

Gluvedus combines metformin, which reduces hepatic glucose production and improves insulin sensitivity, with vildagliptin, a DPP‑4 inhibitor that increases endogenous incretin levels to enhance glucose‑dependent insulin secretion.

It is prescribed for adults with type 2 diabetes mellitus who need additional glycemic control beyond diet, exercise, and metformin monotherapy.

Renal function should be evaluated before initiating Gluvedus; it is generally avoided in patients with severe renal impairment due to the risk of metformin‑associated lactic acidosis.

Common side effects include nausea, diarrhea, headache, mild upper respiratory symptoms, and occasional mild hypoglycemia, especially when used with other glucose‑lowering agents.

Serious reactions such as lactic acidosis, severe hypoglycemia, pancreatitis, severe allergic reactions, or signs of hepatic dysfunction should be reported to a healthcare professional promptly.

Yes, Gluvedus should be discontinued before undergoing radiographic studies that use iodinated contrast media to reduce the risk of renal impairment and lactic acidosis.

The pregnancy safety category for Gluvedus is not established; clinicians should weigh potential benefits against risks and consider alternative therapies when possible.

Excessive alcohol intake can increase the risk of metformin‑related lactic acidosis, so patients are advised to limit alcohol while taking Gluvedus.

Yes, but dose adjustments and close monitoring for hypoglycemia are recommended when Gluvedus is used together with insulin.

Regular monitoring of blood glucose, renal function, and liver enzymes is advised, along with periodic assessment for any adverse effects.

Patients should follow a balanced diet and maintain consistent carbohydrate intake; specific restrictions are not required, but adherence to dietary recommendations supports optimal glycemic control.

If a dose is missed, take it as soon as remembered unless it is close to the time of the next scheduled dose; do not double the dose. Consult a healthcare provider for personalized guidance.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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