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 tablet for oral use. It is indicated for the treatment of idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and in combination therapy for non‑small cell lung cancer.

GNH India supplies Nintedanib Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory support for cross‑border procurement, ensuring timely delivery and product integrity.

Manufacturer / TM Owner

Teva Gmbh

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Indications & Clinical Uses

Nintedanib is employed to treat fibrotic lung conditions and as part of combination regimens for certain cancers, acting on pathways that drive fibroblast activity and tumor angiogenesis.

  • Idiopathic pulmonary fibrosis: slows disease progression and reduces decline in lung function.
  • Systemic sclerosis‑associated interstitial lung disease: helps preserve pulmonary capacity and delays worsening.
  • Non‑small cell lung cancer (in combination therapy): contributes to tumor growth inhibition when used with standard chemotherapy.

How It Works

  • Nintedanib blocks several receptor tyrosine kinases, notably VEGFR 1‑3, PDGFR‑α/β and FGFR 1‑3. Inhibition of these pathways reduces fibroblast proliferation, extracellular matrix deposition and angiogenesis, thereby attenuating fibrotic remodeling in the lung and limiting tumor vascular support.

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 manageable with dietary measures.
  • Nausea: mild to moderate feeling of queasiness.
  • Vomiting: occasional episodes of stomach emptying.
  • Elevated liver enzymes: increase in ALT/AST observed in laboratory tests.

Serious or Rare Side Effects

  • Hepatotoxicity: severe liver injury requiring monitoring and possible discontinuation.
  • Bleeding events: increased risk of gastrointestinal or other bleeding.
  • Cardiovascular events: rare cases of arterial thromboembolism.

Precautions & Warnings

When prescribing Nintedanib, clinicians should observe several precautionary measures to ensure patient safety.

  • Liver function monitoring: assess ALT, AST, and bilirubin before treatment and periodically thereafter.
  • Gastrointestinal management: advise patients to stay hydrated and report severe diarrhea promptly.
  • Drug interactions: review concomitant medications that affect CYP3A4 metabolism.
  • Pregnancy and lactation: avoid use due to unknown fetal risk; discontinue if pregnancy occurs.
  • Contraindications: do not use in patients with severe hepatic impairment.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Nintedanib can interact with other medicines, influencing its efficacy or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase nintedanib exposure and toxicity.
  • Anticoagulants (e.g., warfarin, direct oral anticoagulants): heightened bleeding risk.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole): may modestly raise plasma levels.
  • P-glycoprotein substrates (e.g., digoxin): potential for altered concentrations.
  • Acid‑reducing agents (e.g., proton pump inhibitors): may reduce absorption, monitor efficacy.

Frequently Asked Questions

Nintedanib Teva is an oral tyrosine kinase inhibitor approved for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and as part of combination therapy for non‑small cell lung cancer. It targets pathways that drive fibrosis and tumor angiogenesis.

The drug blocks multiple receptor tyrosine kinases, including VEGFR, PDGFR and FGFR. By inhibiting these signals it reduces fibroblast proliferation, extracellular matrix formation and new blood‑vessel growth, which together limit fibrotic tissue remodeling and tumor vascular support.

Dosing is individualized and set by the prescribing clinician based on the specific indication, patient characteristics and tolerability. Patients should follow the dose and schedule provided in their prescription.

Safety data in pregnancy and lactation are limited, and the drug is classified as having an unknown risk to the fetus. It is generally avoided in pregnant or nursing women, and effective contraception is recommended during treatment.

Enquiries are submitted through the product page at gnhindia.com, where you specify the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

For idiopathic pulmonary fibrosis, the primary alternative is pirfenidone, another antifibrotic agent. Nintedanib targets a broader range of kinases and may be preferred when patients have concomitant vascular involvement, while pirfenidone has a different side‑effect profile, notably photosensitivity.

Store the tablets at ambient temperature, preferably below 25 °C. Keep them in the original packaging, protect from moisture and direct sunlight, and keep out of reach of children.

Nintedanib is taken orally, usually with food to lessen gastrointestinal upset. The tablets are swallowed whole with a glass of water; patients should not crush or split them unless specifically instructed by a healthcare professional.

Serious adverse events include hepatotoxic

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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