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 the treatment of idiopathic pulmonary fibrosis and certain forms of non‑small cell lung cancer, helping to slow disease progression in adult patients.

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‑approved batches to meet global demand.

Manufacturer / TM Owner

Teva Pharmaceuticals Polska Sp. Z O.O.

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Indications & Clinical Uses

Nintedanib acts on fibrotic and oncogenic pathways, providing therapeutic benefit in specific pulmonary and oncologic conditions.

  • Idiopathic pulmonary fibrosis: slows the decline in lung function and reduces disease progression.
  • Non‑small cell lung cancer: used in combination regimens to inhibit tumor angiogenesis and 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 pathways, the drug reduces fibroblast proliferation, angiogenesis, and extracellular matrix deposition, thereby attenuating fibrotic remodeling and tumor vascularization.

Side Effects

Adverse reactions may occur with Nintedanib treatment and are categorized by frequency and severity.

Common Side Effects

  • Diarrhea: frequent, often mild to moderate.
  • Nausea: occasional, may be transient.
  • Vomiting: occasional, usually mild.
  • Decreased appetite: reported in some patients.
  • Abdominal pain: mild to moderate.
  • Headache: occasional.

Serious or Rare Side Effects

  • Elevated liver enzymes (ALT, AST): may indicate hepatic injury.
  • Bleeding events: including gastrointestinal hemorrhage.
  • Gastrointestinal perforation: rare but potentially life‑threatening.
  • Arterial thromboembolic events: such as myocardial infarction or stroke.
  • Severe infections: opportunistic infections have been reported.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor for adverse events.

  • Liver function monitoring: check ALT, AST, and bilirubin before and during treatment.
  • Cardiovascular assessment: evaluate history of ischemic heart disease or thromboembolic disorders.
  • Bleeding risk: avoid concomitant use of strong anticoagulants unless necessary.
  • Gastrointestinal health: use caution in patients with a history of ulcer disease or perforation.
  • Pregnancy and lactation: avoid use unless benefits outweigh potential risks.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

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, itraconazole): may raise nintedanib exposure.
  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic effect.
  • Anticoagulants (e.g., warfarin) and antiplatelet agents (e.g., aspirin): increase bleeding potential.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., erythromycin, fluconazole): may modestly increase plasma levels.
  • P‑gp/BCRP inhibitors (e.g., verapamil): may slightly elevate exposure.
  • Diuretics: monitor electrolytes as nintedanib can affect renal handling.

Frequently Asked Questions

Nintedanib Teva is prescribed for adult patients with idiopathic pulmonary fibrosis to slow lung function decline, and for certain cases of non‑small cell lung cancer where it is combined with other anticancer agents to inhibit tumor growth and angiogenesis.

Nintedanib blocks several receptor tyrosine kinases—VEGFR, FGFR, and PDGFR—thereby reducing fibroblast activity, new blood‑vessel formation, and the deposition of scar tissue. This dual antifibrotic and anti‑angiogenic action underlies its therapeutic effects in lung fibrosis and cancer.

The specific dose and dosing schedule of Nintedanib Teva are determined by the prescribing physician based on the patient’s condition, weight, renal and hepatic function, and other clinical factors. Patients should follow the prescriber’s instructions exactly.

Safety data for Nintedanib Teva in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To request Nintedanib Teva, submit an enquiry on the product page at gnhindia.com indicating 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 necessary import documentation.

Nintedanib differs from other antifibrotics such as pirfenidone by targeting a broader range of tyrosine kinases, which gives it both antifibrotic and anti‑angiogenic properties. Clinical studies show comparable efficacy in slowing lung function decline, but the side‑effect profile and drug‑interaction potential vary, so choice depends on individual patient factors.

Nintedanib Teva should be stored at temperatures below 25 °C, in its original packaging, protected from moisture and direct sunlight. Do not store in a bathroom or near a heat source, and keep the container tightly closed when not in use.

Nintedanib Teva is taken orally, usually with food to reduce gastrointestinal discomfort. The tablets are swallowed whole with a glass of water and should be taken at the same time each day as directed by the prescriber.

Serious risks include significant liver enzyme elevations, gastrointestinal bleeding, and rare events such as intestinal perforation or arterial thromboembolic episodes. Patients should be monitored regularly for liver function, signs of bleeding, and any new severe abdominal symptoms.

Nintedanib Teva is contraindicated in patients with severe hepatic impairment, active bleeding disorders, recent major surgery involving the gastrointestinal tract, or known hypersensitivity to nintedanib or any excipients. It should also be used with caution in those with uncontrolled cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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