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

Nintedanib Teva

Active Ingredient:
Nintedanib
Origin:
EU

Nintedanib Teva (Nintedanib)

Nintedanib, the active ingredient in Nintedanib Teva, is a tyrosine kinase inhibitor presented as a tablet for oral use. It targets key pathways involved in fibrotic lung disease and certain cancers, and is indicated for the treatment of idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and specific non‑small cell lung cancer subtypes.

GNH India supplies Nintedanib Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, oncology centres and clinics worldwide, ensuring quality assurance and regulatory compliance across all markets.

Manufacturer / TM Owner

Teva Gmbh

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Indications & Clinical Uses

  • Nintedanib is used in fibrotic lung disorders and selected oncologic indications, where it modulates disease‑driving pathways.
  • Idiopathic pulmonary fibrosis: slows decline in lung function and reduces disease progression.
  • Systemic sclerosis‑associated interstitial lung disease: improves pulmonary function and delays worsening.
  • Non‑small cell lung cancer: used in combination therapy to inhibit tumor growth.

How It Works

  • Nintedanib inhibits multiple receptor tyrosine kinases, including vascular endothelial growth factor receptors (VEGFR 1‑3), fibroblast growth factor receptors (FGFR 1‑3) and platelet‑derived growth factor receptors (PDGFR‑α/β). By blocking these signaling pathways, the drug reduces fibroblast proliferation, angiogenesis, and extracellular matrix deposition, thereby limiting fibrotic tissue formation and tumor angiogenesis.

Side Effects

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

Common Side Effects

  • Diarrhea: frequent loose stools.
  • Nausea: mild to moderate sensation.
  • Vomiting: occasional episodes.
  • Elevated liver enzymes: increased ALT/AST levels.

Serious or Rare Side Effects

  • Hepatotoxicity: severe liver injury requiring monitoring.
  • Bleeding events: heightened risk of gastrointestinal or intracranial hemorrhage.
  • Cardiovascular events: arterial thromboembolism or myocardial infarction.

Precautions & Warnings

  • When prescribing Nintedanib, clinicians should consider several safety measures.
  • Liver function monitoring: perform baseline and periodic ALT/AST tests.
  • Bleeding risk assessment: avoid concomitant anticoagulants unless necessary.
  • Gastrointestinal health: monitor for severe diarrhea or colitis.
  • Pregnancy and lactation: use only if benefits outweigh risks; consult physician.
  • Drug interactions: review concomitant medications for CYP3A4 substrates.
  • Store at below 25°C: keep in original packaging, protect from moisture and light.

Avoid Interactions

Nintedanib can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase nintedanib exposure.
  • Anticoagulants (e.g., warfarin, direct oral anticoagulants): heightened bleeding risk.
  • P‑glycoprotein inhibitors (e.g., verapamil): may raise plasma levels.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy.
  • Antiplatelet agents (e.g., aspirin, clopidogrel): monitor for bleeding.
  • Diuretics: watch for dehydration that can worsen gastrointestinal side effects.

Frequently Asked Questions

Nintedanib Teva is approved for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and certain forms of non‑small cell lung cancer. In each case, the drug aims to slow disease progression by targeting pathways that drive fibrosis and tumor growth.

Nintedanib blocks several receptor tyrosine kinases—VEGFR, FGFR and PDGFR—thereby reducing fibroblast proliferation, angiogenesis, and extracellular matrix deposition. This dual antifibrotic and anti‑angiogenic action helps limit scar tissue formation in the lungs and restricts blood‑vessel growth that supports tumor cells.

The exact dose and schedule are set by the prescribing clinician based on the patient’s specific indication, disease severity, renal and hepatic function, and any concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Data on the use of nintedanib in pregnant or nursing women are limited. The drug should only be used if the potential benefit justifies the potential risk to the fetus or infant, and treatment decisions should be made in consultation with a healthcare professional.

To request Nintedanib Teva, 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 required import documentation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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