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

Nintedanib Teva Gmbh

Active Ingredient:
Nintedanib
Origin:
EU

Nintedanib Teva Gmbh (Nintedanib)

Nintedanib, the active ingredient in Nintedanib Teva Gmbh, is a tyrosine kinase inhibitor presented as a capsule for oral use. It treats idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and is used with docetaxel in non‑small cell lung cancer.

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

Manufacturer / TM Owner

Teva Gmbh

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Indications & Clinical Uses

Nintedanib is indicated for fibrotic lung disorders and certain cancer regimens.

  • Idiopathic pulmonary fibrosis: slows disease progression and reduces decline in lung function.
  • Systemic sclerosis‑associated interstitial lung disease: improves lung capacity and delays worsening.
  • Non‑small cell lung cancer (in combination with docetaxel): enhances response rates and overall survival.

How It Works

  • Nintedanib inhibits 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 blocking these pathways, it reduces fibroblast proliferation, migration, and transformation, leading to antifibrotic and anti‑angiogenic effects that limit tissue scarring 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, often mild to moderate.
  • Nausea: feeling of sickness or urge to vomit.
  • Vomiting: occasional episodes of expulsion of stomach contents.
  • Elevated liver enzymes: increase in ALT/AST observed in blood tests.

Serious or Rare Side Effects

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

Precautions & Warnings

Before prescribing Nintedanib, clinicians should consider several precautionary measures.

  • Liver function monitoring: assess ALT, AST, bilirubin before and during therapy.
  • Gastrointestinal management: advise patients to stay hydrated and report severe diarrhea.
  • Drug interactions: review concomitant medications that affect CYP3A4.
  • Pregnancy contraindication: avoid use in pregnant women; teratogenic risk.
  • Bleeding risk: evaluate patients with history of ulcers or anticoagulant use.
  • Store at ambient temperature: keep below 25°C in original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole): may modestly raise levels.
  • P-glycoprotein substrates (e.g., digoxin): potential altered concentrations.
  • Antacids or proton pump inhibitors: may affect absorption; monitor GI tolerance.

Frequently Asked Questions

Nintedanib Teva Gmbh is prescribed for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and in combination with docetaxel for non‑small cell lung cancer. In each case it aims to slow disease progression, preserve lung function, or improve cancer treatment outcomes.

Nintedanib blocks several receptor tyrosine kinases—VEGFR, PDGFR and FGFR—thereby reducing fibroblast activity and angiogenesis. This dual antifibrotic and anti‑angiogenic action limits tissue scarring in lung disease and hampers tumor blood‑vessel formation in cancer.

The exact dose and schedule of Nintedanib are determined by the prescribing clinician based on the specific indication, patient characteristics and any concomitant therapies. Patients should follow the individualized regimen provided by their healthcare professional.

Nintedanib is contraindicated during pregnancy because it may cause fetal harm. Women of childbearing potential should use effective contraception. Breastfeeding is not recommended while taking Nintedanib, as safety for the infant has not been established.

To 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.

The primary alternative for idiopathic pulmonary fibrosis is pirfenidone, another antifibrotic agent. While both aim to slow lung function decline, Nintedanib targets multiple tyrosine kinases and is also approved for certain cancers, whereas pirfenidone has a different safety profile, notably fewer gastrointestinal effects but more photosensitivity.

Nintedanib capsules should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect them from moisture and direct sunlight. Do not refrigerate or freeze the product.

Nintedanib is taken orally as a capsule, usually with food to lessen gastrointestinal discomfort. Patients should swallow the capsule whole with water and follow the dosing schedule prescribed by their clinician.

Serious risks include liver injury (hepatotoxicity), significant bleeding events, and rare cardiovascular complications such as arterial thromboembolism. Patients should be monitored regularly for liver enzyme elevations and signs of bleeding, and any concerning symptoms should be reported promptly.

Nintedanib should not be used by pregnant women, individuals with severe liver impairment, or patients with uncontrolled bleeding disorders. Caution is also advised for those on strong CYP3A4 inhibitors or anticoagulants, and the drug is contraindicated in patients with known hypersensitivity to its components.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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