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 an oral formulation for oral use. It is indicated for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and non‑small cell lung cancer in appropriate patients.

GNH India supplies Nintedanib Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Pharmaceuticals S.R.L

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Indications & Clinical Uses

  • Nintedanib is used to treat fibrotic lung disorders and certain cancers by targeting multiple growth factor pathways.
  • Idiopathic pulmonary fibrosis: slows disease progression and reduces decline in lung function.
  • Systemic sclerosis‑associated interstitial lung disease: improves lung capacity and delays functional deterioration.
  • Non‑small cell lung cancer: used in combination regimens to inhibit tumor angiogenesis and growth.

How It Works

  • Nintedanib inhibits several 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 blocking these pathways, it reduces fibroblast proliferation, angiogenesis, and extracellular matrix deposition, thereby attenuating fibrotic processes and tumor vascularization.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Diarrhea: mild to moderate, often manageable with supportive care.
  • Nausea: occasional, may improve over time.
  • Elevated liver enzymes: transient increases in ALT/AST.
  • Decreased appetite: reduced food intake.
  • Vomiting: occasional episodes.
  • Abdominal pain: mild discomfort.

Serious or Rare Side Effects

  • Hepatotoxicity: significant liver injury requiring monitoring.
  • Cardiovascular events: rare cases of arterial thromboembolism.
  • Severe bleeding: especially in patients on anticoagulants.
  • Interstitial lung disease exacerbation: rare worsening of underlying disease.
  • Severe hypersensitivity: rash, angioedema, or anaphylaxis.
  • Gastrointestinal perforation: extremely rare but serious.

Precautions & Warnings

  • Patients should be monitored for organ function and potential adverse events.
  • Liver function monitoring: check ALT/AST before starting and periodically during therapy.
  • Cardiovascular assessment: evaluate risk factors for arterial events.
  • Bleeding risk: avoid concomitant anticoagulants unless necessary.
  • Pregnancy and lactation: discuss risks with a healthcare professional.
  • Drug interactions: review all concomitant medications for potential interactions.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture and light.

Avoid Interactions

Nintedanib may interact with other medicines that affect its metabolism or increase bleeding risk.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise nintedanib exposure.
  • Anticoagulants (e.g., warfarin, direct oral anticoagulants): increase bleeding risk.
  • Antiplatelet agents (e.g., aspirin, clopidogrel): additive hemorrhagic potential.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole): may modestly increase levels.
  • P‑glycoprotein inhibitors (e.g., verapamil): could affect absorption.
  • CYP3A4 inducers (e.g., rifampicin): may reduce efficacy.
  • NSAIDs: monitor for gastrointestinal bleeding.
  • Herbal supplements affecting liver enzymes: assess on a case‑by‑case basis.

Frequently Asked Questions

Nintedanib Teva is prescribed for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and non‑small cell lung cancer. In each case, it works by inhibiting pathways that drive fibrosis or tumor angiogenesis, helping to slow disease progression.

Nintedanib blocks multiple receptor tyrosine kinases—VEGFR, PDGFR, and FGFR—thereby reducing fibroblast activity, new blood‑vessel formation, and extracellular matrix deposition. This dual antifibrotic and anti‑angiogenic action underlies its therapeutic effects in lung fibrosis and certain cancers.

The specific dose and dosing schedule of Nintedanib Teva are determined by the prescribing clinician based on the patient’s condition, weight, renal and hepatic function, and other individual factors. Patients should follow the exact regimen provided by their healthcare professional.

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 who are pregnant, planning to become pregnant, or breastfeeding should discuss alternatives with their physician.

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 needs), and import documentation.

Nintedanib differs from pirfenidone, another antifibrotic, by targeting a broader range of tyrosine kinases (VEGFR, PDGFR, FGFR). This broader inhibition may offer benefits in certain interstitial lung diseases and in combination cancer regimens, while the safety profile and tolerability can vary between the two agents.

Nintedanib Teva should be stored at ambient temperature, below 25 °C. Keep the product in its original packaging, protect it from moisture and direct light, and ensure the container is tightly closed when not in use.

Nintedanib Teva is taken orally, usually with food to reduce gastrointestinal discomfort. The tablets (or capsules) are swallowed whole with a full glass of water and should not be crushed, chewed, or split unless directed by a healthcare professional.

Serious risks include liver injury (elevated transaminases), severe bleeding, arterial thromboembolic events, and rare cases of gastrointestinal perforation. Patients should be monitored regularly for liver function, signs of bleeding, and any new cardiovascular symptoms.

Nintedanib is contraindicated in patients with known hypersensitivity to the drug or any of its excipients, those with severe liver impairment, and individuals currently receiving strong CYP3A4 inhibitors. Clinicians should also assess bleeding risk before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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