Product image of Linagliptin-Metformin Linagliptin-Metformin Stada 2,5 Mg/500 Mg Filmtabletta (Metformin Hydrochloride, Linagliptin) supplied by GNH India

Linagliptin-Metformin Linagliptin-Metformin Stada 2,5 Mg/500 Mg Filmtabletta

Active Ingredient:
Metformin Hydrochloride, Linagliptin
Origin:
EU

Linagliptin-Metformin Linagliptin-Metformin Stada 2,5 Mg/500 Mg Filmtabletta (Metformin Hydrochloride, Linagliptin)

Linagliptin, the active ingredient in Linagliptin‑Metformin Stada 2,5 Mg/500 Mg Filmtabletta, is a DPP‑4 inhibitor presented as a 2.5 mg/500 mg film‑coated tablet for oral use. It treats type 2 diabetes mellitus in adults, often in combination with diet and exercise.

GNH India supplies Linagliptin‑Metformin Stada 2,5 Mg/500 Mg Filmtabletta as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Linagliptin/Metformin is indicated for the management of type 2 diabetes mellitus, targeting hyperglycaemia through complementary mechanisms.

  • Type 2 diabetes mellitus: improves glycaemic control as part of combination therapy.
  • Inadequate control on metformin alone: adds DPP‑4 inhibition to further lower HbA1c.
  • Fixed‑dose combination therapy: simplifies regimen and enhances patient adherence.

How It Works

  • Linagliptin selectively inhibits dipeptidyl peptidase‑4, raising endogenous GLP‑1 levels and promoting glucose‑dependent insulin secretion. Metformin hydrochloride suppresses hepatic gluconeogenesis, reduces intestinal glucose absorption, and increases peripheral insulin sensitivity, together providing additive glucose‑lowering effects in type 2 diabetes.

Side Effects

Common Side Effects

  • Nausea: mild to moderate gastrointestinal discomfort.
  • Diarrhoea: loose stools, usually transient.
  • Headache: mild tension‑type pain.
  • Nasopharyngitis: upper respiratory symptoms.
  • Dizziness: occasional light‑headedness.
  • Abdominal pain: mild cramping.

Serious or Rare Side Effects

  • Lactic acidosis: rare but life‑threatening metabolic disturbance.
  • Pancreatitis: severe abdominal pain with elevated enzymes.
  • Severe hypersensitivity: rash, angioedema, or anaphylaxis.
  • Hepatic failure: signs of liver dysfunction.
  • Hypoglycaemia: when combined with insulin or sulfonylureas.
  • Renal impairment: worsening kidney function may occur.

Precautions & Warnings

Before initiating therapy, evaluate patient-specific risk factors and monitor regularly.

  • Renal function assessment: check eGFR prior to start and periodically thereafter.
  • Hepatic impairment: use with caution in patients with liver disease.
  • Risk of lactic acidosis: avoid in severe renal or hepatic dysfunction.
  • Pregnancy and lactation: safety not established; consider alternative agents.
  • Drug interactions: review concomitant medicines that affect renal clearance or increase hypoglycaemia risk.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture.

Avoid Interactions

Linagliptin/Metformin may interact with several medicines; monitor and adjust therapy as needed.

Major Interactions (Avoid)

  • Severe renal impairment (eGFR <30 mL/min/1.73 m²): contraindicated.
  • Co‑administration with other DPP‑4 inhibitors: duplicate therapy risk.
  • Use with high‑dose metformin in hepatic failure: heightened lactic acidosis risk.

Moderate Interactions (Monitor Closely)

  • Sulfonylureas or insulin: increased hypoglycaemia potential.
  • Iodinated contrast media: temporary renal function decline; monitor renal parameters.

Frequently Asked Questions

Linagliptin‑Metformin Stada is prescribed to improve blood‑sugar control in adults with type 2 diabetes mellitus, usually as part of a comprehensive plan that includes diet, exercise, and other antidiabetic agents when needed.

Linagliptin blocks the enzyme dipeptidyl peptidase‑4, which raises levels of incretin hormones such as GLP‑1. This enhances glucose‑dependent insulin release and reduces glucagon secretion, helping to lower post‑prandial glucose.

The specific dose and dosing schedule are determined by the prescribing healthcare professional based on the individual’s clinical condition, renal function, and response to therapy.

Safety in pregnancy and lactation has not been established. Clinicians usually consider alternative treatments for pregnant or nursing women unless the benefits outweigh potential risks.

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 separate tablets of linagliptin and metformin, the fixed‑dose combination simplifies the regimen, reduces pill burden and may improve adherence, while delivering the same pharmacologic actions of a DPP‑4 inhibitor plus a biguanide.

Store the film‑coated tablets at ambient temperature, preferably below 25 °C, in the original container to protect them from moisture and light.

The tablet is taken orally, usually with or without food, as directed by the prescriber. Swallow the tablet whole; do not split, crush, or chew unless advised otherwise.

Serious concerns include lactic acidosis (especially in patients with renal or hepatic impairment), pancreatitis, severe hypersensitivity reactions, and hypoglycaemia when combined with insulin or sulfonylureas.

Patients with severe renal impairment (eGFR <30 mL/min/1.73 m²), known hypersensitivity to either component, or those with acute or chronic metabolic acidosis, including lactic acidosis, should avoid this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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