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

Nintedanib Eg

Active Ingredient:
Nintedanib
Origin:
EU

Nintedanib Eg (Nintedanib)

Nintedanib, the active ingredient in Nintedanib Eg, is a tyrosine kinase inhibitor presented as an oral capsule for oral use. It is indicated for certain fibrotic lung conditions and for use in combination therapy for non‑small cell lung cancer.
GNH India supplies Nintedanib Eg as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Eg S.P.A.

1
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Indications & Clinical Uses

Nintedanib acts on pathways that drive fibrosis and tumor angiogenesis, making it useful in several serious respiratory and oncologic conditions.

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

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, angiogenesis, and extracellular matrix deposition, thereby attenuating fibrotic processes and tumor vascularization.

Side Effects

Nintedanib may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Diarrhoea: frequent loose stools, often mild to moderate.
  • Nausea: feeling of sickness, may be transient.
  • Vomiting: occasional episodes, usually self‑limiting.
  • Decreased appetite: reduced desire to eat.
  • Liver enzyme elevation: mild increases in ALT/AST.
  • Abdominal pain: discomfort in the stomach area.

Serious or Rare Side Effects

  • Severe liver injury: marked elevation of liver enzymes or hepatitis.
  • Gastrointestinal perforation: rare but potentially life‑threatening.
  • Cardiovascular events: such as myocardial infarction or stroke.
  • Severe bleeding: especially in patients on anticoagulants.
  • Interstitial lung disease exacerbation: worsening of underlying lung disease.
  • Allergic reactions: including rash, urticaria, or anaphylaxis.

Precautions & Warnings

Before initiating therapy, clinicians should assess baseline organ function and review concomitant medications.

  • Liver function monitoring: obtain baseline ALT/AST and repeat periodically.
  • Gastrointestinal assessment: monitor for persistent diarrhoea or abdominal pain.
  • Bleeding risk: evaluate patients on anticoagulants or with a history of bleeding.
  • Pregnancy and lactation: avoid use unless benefits outweigh potential risks.
  • Storage: Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Nintedanib can interact with several drug classes, 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.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole): may modestly raise plasma levels.
  • P-glycoprotein inhibitors (e.g., verapamil): could increase systemic exposure.
  • CYP3A4 inducers (e.g., rifampicin): may reduce efficacy by lowering drug concentrations.

Frequently Asked Questions

Nintedanib Eg is prescribed for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and as part of combination therapy for non‑small cell lung cancer. It targets the underlying fibrotic and angiogenic pathways that drive disease progression.

Nintedanib blocks several receptor tyrosine kinases—VEGFR, PDGFR, and FGFR—thereby reducing fibroblast growth, new blood‑vessel formation, and extracellular matrix production. This inhibition helps slow fibrosis and can limit tumor vascularization when used with other anticancer agents.

The specific dose and dosing schedule for Nintedanib Eg 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 prescriber’s instructions exactly.

The safety of Nintedanib in pregnancy or while breastfeeding has not been established. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and this decision must be made by a qualified healthcare professional.

To request Nintedanib Eg, 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 necessary import documentation.

Nintedanib differs from other antifibrotics such as pirfenidone by targeting a broader range of tyrosine kinases (VEGFR, PDGFR, FGFR). This multi‑target approach may offer additional benefits in certain fibrotic lung diseases, though individual response and safety profiles vary and should be evaluated by the treating physician.

Nintedanib Eg capsules should be stored at temperatures below 25 °C, in the original packaging, and protected from moisture. Do not expose the product to excessive heat or humidity to maintain its stability and potency.

Nintedanib Eg is taken orally as a capsule with water. It is usually administered with food to reduce gastrointestinal discomfort, but patients should follow the specific instructions provided by their healthcare provider.

Serious risks include severe liver injury, gastrointestinal perforation, major bleeding events, and rare cardiovascular complications such as myocardial infarction or stroke. Patients should be monitored regularly for signs of these events and report any concerning symptoms promptly.

Nintedanib is contraindicated in patients with known hypersensitivity to the drug or any of its excipients, and it should be avoided in individuals with severe hepatic impairment. Clinicians should also exercise caution in patients with a high bleeding risk or uncontrolled cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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