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 tablet for oral use. It is classified as an antifibrotic agent and is indicated for the treatment of idiopathic pulmonary fibrosis and for use in combination therapy for certain non‑small cell lung cancers in adult patients.

GNH India supplies Nintedanib Eg as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide, providing reliable sourcing for clinical and research needs and ensuring compliance with regulatory standards.

Manufacturer / TM Owner

Eurogenerics N.V./S.A.

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Indications & Clinical Uses

Nintedanib acts on fibrotic and oncogenic pathways, making it useful in several pulmonary and cancer indications.

  • Idiopathic pulmonary fibrosis: reduces the rate of forced vital capacity decline.
  • Systemic sclerosis‑associated interstitial lung disease: helps preserve lung function.
  • Non‑small cell lung cancer (in combination with chemotherapy): improves progression‑free 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, the drug decreases fibroblast proliferation, angiogenesis, and extracellular matrix deposition, thereby attenuating fibrotic remodeling and tumor‑driven vascular growth.

Side Effects

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

Common Side Effects

  • Diarrhea: frequent loose stools, often mild to moderate.
  • Nausea and vomiting: gastrointestinal upset that may affect appetite.
  • Decreased appetite: reduced food intake leading to weight loss.
  • Elevated liver enzymes: mild transaminase increases detected on routine labs.

Serious or Rare Side Effects

  • Severe liver injury: jaundice, hepatic failure requiring monitoring.
  • Major bleeding events: gastrointestinal or intracranial hemorrhage, especially with anticoagulants.
  • Cardiovascular complications: hypertension, arterial thrombotic events, or heart failure.
  • Gastrointestinal perforation: rare but potentially life‑threatening.
  • Severe infections: opportunistic infections in immunocompromised patients.

Precautions & Warnings

Before initiating therapy, clinicians should assess baseline organ function and counsel patients on potential risks.

  • Liver monitoring: perform baseline and periodic liver function tests.
  • Cardiovascular assessment: evaluate blood pressure and cardiac history.
  • Bleeding risk: review concomitant anticoagulant or antiplatelet use.
  • Gastrointestinal symptoms: advise patients to report persistent diarrhea or abdominal pain.
  • Pregnancy and lactation: avoid use unless benefits outweigh potential fetal risks.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nintedanib can interact with several drug classes, influencing its exposure or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): increase nintedanib plasma levels.
  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): markedly reduce nintedanib exposure.
  • Anticoagulants (e.g., warfarin, direct oral anticoagulants): may heighten bleeding risk.

Moderate Interactions (Monitor Closely)

  • P‑gp inhibitors (e.g., verapamil, amiodarone): modestly raise nintedanib concentrations.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase gastrointestinal bleeding potential.
  • Diuretics and antihypertensives: may exacerbate hypotension or electrolyte disturbances.

Frequently Asked Questions

Nintedanib Eg is prescribed for adults with idiopathic pulmonary fibrosis to slow lung function decline, for systemic sclerosis‑associated interstitial lung disease to preserve pulmonary capacity, and in combination with chemotherapy for certain non‑small cell lung cancers to improve progression‑free survival.

The drug blocks several receptor tyrosine kinases—VEGFR, PDGFR, and FGFR—thereby reducing fibroblast growth, new blood‑vessel formation, and extracellular matrix production. This dual antifibrotic and anti‑angiogenic action helps limit tissue scarring and tumor‑driven vascular development.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s indication, renal and hepatic function, and concomitant therapies. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

The safety of Nintedanib in pregnancy and lactation has not been established. It should be used only if the potential benefit justifies the potential risk to the fetus, and breastfeeding mothers should discuss alternatives with their healthcare provider.

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 (including any cold‑chain needs) and the necessary import documentation.

Compared with alternatives such as pirfenidone, Nintedanib targets a broader range of tyrosine kinases, offering both antifibrotic and anti‑angiogenic effects. Clinical trials have shown comparable efficacy in slowing lung function decline, but the side‑effect profile differs, with gastrointestinal events being more common with Nintedanib.

Store Nintedanib Eg at room temperature, below 25 °C, in the original packaging. Keep the product away from moisture, excessive heat and direct sunlight to maintain stability and potency.

Nintedanib Eg is taken orally, usually with food to reduce gastrointestinal upset. The tablets should be swallowed whole with a glass of water and not crushed or chewed unless directed by a healthcare professional.

Serious risks include severe liver injury, major bleeding events, cardiovascular complications such as hypertension or arterial thrombotic episodes, gastrointestinal perforation, and opportunistic infections. Patients should be monitored regularly for signs of these conditions.

Nintedanib is contraindicated in patients with severe hepatic impairment, uncontrolled bleeding disorders, or known hypersensitivity to the drug. Caution is also advised for individuals with significant cardiovascular disease, active infections, or those taking strong CYP3A4 inducers or inhibitors without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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