Product image of Nintedanib Eugia (Nintedanib) supplied by GNH India

Nintedanib Eugia

Active Ingredient:
Nintedanib
Origin:
EU

Nintedanib Eugia (Nintedanib)

Nintedanib, the active ingredient in Nintedanib Eugia, is a tyrosine kinase inhibitor presented as an oral formulation for oral use. It is indicated for the treatment of idiopathic pulmonary fibrosis, certain forms of non‑small cell lung cancer, and systemic sclerosis‑associated interstitial lung disease in adult patients.

GNH India supplies Nintedanib Eugia as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide. The company ensures quality compliance with EU standards and provides reliable logistics for global distribution.

Manufacturer / TM Owner

Eugia Pharma (Malta) Ltd

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Indications & Clinical Uses

Nintedanib is used in fibrotic lung disorders and selected oncologic indications, targeting pathways that drive fibroblast activity and tumor growth.

  • Idiopathic pulmonary fibrosis: slows disease progression and reduces decline in lung function.
  • Non‑small cell lung cancer: used in combination therapy to inhibit tumor angiogenesis and growth.
  • Systemic sclerosis‑associated interstitial lung disease: helps preserve pulmonary capacity and limit fibrotic remodeling.

How It Works

  • Nintedanib blocks multiple receptor tyrosine kinases, including vascular endothelial growth factor receptors (VEGFR 1‑3), platelet‑derived growth factor receptors (PDGFR‑α/β) and fibroblast growth factor receptors (FGFR 1‑3). By inhibiting these pathways, the drug reduces endothelial cell proliferation, fibroblast activation, and extracellular matrix deposition, thereby attenuating angiogenesis and fibrotic tissue formation in the lungs and other affected organs.

Side Effects

Nintedanib may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Diarrhea: frequent loose stools, often mild to moderate.
  • Nausea: feeling of sickness, may accompany meals.
  • Decreased appetite: reduced desire to eat, sometimes leading to weight loss.

Serious or Rare Side Effects

  • Elevated liver enzymes: may indicate hepatic injury, requires monitoring.
  • Bleeding events: increased risk of gastrointestinal or other hemorrhage.
  • Cardiovascular complications: such as hypertension or arterial thrombotic events.

Precautions & Warnings

When prescribing Nintedanib, clinicians should observe several safety considerations to minimize risk.

  • Monitor liver function: perform baseline and periodic ALT/AST tests.
  • Assess bleeding risk: avoid in patients with active ulcers or on anticoagulants.
  • Evaluate cardiovascular status: watch for hypertension or thrombotic events.
  • Avoid use in severe hepatic impairment: contraindicated in patients with Child‑Pugh C.
  • Adjust for drug interactions: review concomitant CYP3A4 modulators.
  • Store at room temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

Nintedanib interacts with several medicines that can alter its exposure or increase adverse effects.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may raise nintedanib plasma levels.
  • Anticoagulants (e.g., warfarin, direct oral anticoagulants): increase risk of serious bleeding.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., erythromycin, clarithromycin): may modestly increase exposure.
  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy by lowering drug levels.
  • P‑glycoprotein inhibitors (e.g., verapamil): can affect absorption.
  • Antacids containing aluminum or magnesium: may decrease oral bioavailability if taken simultaneously.

Frequently Asked Questions

Nintedanib Eugia is prescribed for adult patients with idiopathic pulmonary fibrosis, certain forms of non‑small cell lung cancer, and systemic sclerosis‑associated interstitial lung disease. In each condition the drug aims to slow disease progression by targeting key pathways involved in fibrosis and tumor angiogenesis.

Nintedanib inhibits multiple receptor tyrosine kinases—VEGFR, PDGFR and FGFR. Blocking these receptors reduces fibroblast proliferation, extracellular matrix deposition, and new blood‑vessel formation, which together limit fibrotic tissue development and tumor growth in the lungs.

The dosage of Nintedanib Eugia is determined by the prescribing clinician based on the specific indication, patient characteristics and any concomitant therapies. The prescriber will set the appropriate strength, frequency and duration according to current clinical guidelines.

Safety data for Nintedanib in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant. Women of child‑bearing potential should use effective contraception during treatment and for a period after the last dose.

To request Nintedanib Eugia, submit an enquiry on the product page at gnhindia.com with 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 needs) and the necessary import documentation.

For idiopathic pulmonary fibrosis, the primary alternative is pirfenidone, another antifibrotic agent. While both aim to slow lung function decline, Nintedanib targets a broader range of tyrosine kinases, which may provide additional benefit in certain patients but can be associated with a higher incidence of gastrointestinal side effects.

Nintedanib Eugia should be stored at room temperature, below 25 °C. Keep the product in its original container, protect it from moisture and direct light, and avoid exposing it to extreme temperatures that could compromise tablet integrity.

The medication is taken orally, usually with food to reduce gastrointestinal discomfort. Patients should swallow the tablet whole with a full glass of water and follow the dosing schedule prescribed by their healthcare professional.

Key serious risks include liver injury (elevated transaminases), bleeding complications, and cardiovascular events such as hypertension or arterial thrombosis. Patients should be monitored regularly for liver function, signs of bleeding, and blood pressure changes throughout therapy.

Nintedanib is contraindicated in patients with severe hepatic impairment (Child‑Pugh C), active uncontrolled bleeding, or known hypersensitivity to the drug. It should also be avoided in pregnancy unless absolutely necessary, and used with caution in individuals with significant cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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