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

Nintedanib Eugia

Active Ingredient:
Nintedanib
Origin:
EU

Nintedanib Eugia (Nintedanib)

Nintedanib, the active ingredient in Nintedanib Eugia, is a tyrosine kinase inhibitor presented as an oral formulation for oral use. It is indicated for the treatment of idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and certain forms of non‑small cell lung cancer in adult patients.

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

Manufacturer / TM Owner

Eugia Pharma (Malta) Ltd

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Indications & Clinical Uses

Nintedanib Eugia acts on multiple receptor tyrosine kinases involved in fibrotic and oncogenic pathways, providing therapeutic benefit in several serious lung conditions.

  • Idiopathic pulmonary fibrosis: slows decline in lung function and reduces disease progression.
  • Systemic sclerosis‑associated interstitial lung disease: mitigates fibrotic changes and preserves respiratory capacity.
  • Non‑small cell lung cancer: used in combination regimens to inhibit tumor growth and angiogenesis.

How It Works

  • Nintedanib inhibits a spectrum of receptor tyrosine kinases—including VEGFR 1‑3, PDGFR α/β, and FGFR 1‑3—thereby reducing fibroblast proliferation, migration, and differentiation. This multi‑target blockade curtails pathological angiogenesis and extracellular matrix deposition, slowing the progression of fibrosis and tumor vascularization.

Side Effects

Nintedanib may cause a range of adverse reactions, from mild to severe. Patients should be monitored regularly for any new symptoms.

Common Side Effects

  • Diarrhea: frequent loose stools, often mild to moderate.
  • Nausea and vomiting: gastrointestinal discomfort.
  • Abdominal pain: cramping or discomfort in the stomach area.
  • Decreased appetite: reduced desire to eat, potentially leading to weight loss.
  • Elevated liver enzymes: mild increases in ALT/AST.
  • Fatigue: general feeling of tiredness.

Serious or Rare Side Effects

  • Severe liver injury: jaundice, marked enzyme elevation, or hepatic failure.
  • Major bleeding events: gastrointestinal or intracranial hemorrhage.
  • Cardiovascular complications: myocardial infarction or stroke.
  • Gastrointestinal perforation: severe abdominal pain requiring urgent care.
  • Severe infections: opportunistic or bacterial infections.
  • Pulmonary embolism: sudden shortness of breath or chest pain.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient-specific risk factors and monitor relevant clinical parameters.

  • Liver function monitoring: check ALT/AST before treatment and periodically thereafter.
  • Bleeding risk assessment: avoid in patients with active bleeding or uncontrolled anticoagulation.
  • Cardiovascular evaluation: caution in patients with recent myocardial infarction or uncontrolled hypertension.
  • Pregnancy and lactation: avoid use due to unknown safety; discuss contraception.
  • Renal impairment: dose adjustment may be required in severe renal dysfunction.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Nintedanib can interact with several drug classes, influencing its efficacy and safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase nintedanib exposure.
  • Potent P‑gp inhibitors (e.g., verapamil): can raise plasma concentrations.
  • Anticoagulants (e.g., warfarin, direct oral anticoagulants): heightened risk of serious bleeding.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce therapeutic effect.
  • Antiplatelet agents (e.g., aspirin, clopidogrel): monitor for additive bleeding risk.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase gastrointestinal bleeding potential.

Frequently Asked Questions

Nintedanib Eugia is prescribed to treat idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and certain types of non‑small cell lung cancer. It works by inhibiting key pathways that drive fibrosis and tumor angiogenesis, helping to slow disease progression and improve lung function.

Nintedanib blocks multiple receptor tyrosine kinases—VEGFR 1‑3, PDGFR α/β, and FGFR 1‑3. By inhibiting these receptors, the drug reduces fibroblast activity, limits new blood‑vessel formation, and curtails the deposition of scar tissue, which together help control fibrotic lung disease and impede cancer growth.

The specific dose of Nintedanib Eugia is determined by the prescribing clinician based on the patient’s condition, weight, renal and hepatic function, and other individual factors. Healthcare professionals follow approved labeling and clinical guidelines when establishing the regimen.

Safety of Nintedanib during pregnancy and lactation has not been established. The product carries an unknown pregnancy category, and it is generally advised to avoid use in pregnant or nursing women unless the potential benefit justifies the potential risk. Contraception should be used during treatment.

To place an 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 required import documentation.

The primary alternative for idiopathic pulmonary fibrosis is pirfenidone, another antifibrotic agent. While both slow disease progression, Nintedanib targets a broader range of tyrosine kinases, offering additional anti‑angiogenic activity useful in certain lung cancers. Choice between them depends on patient tolerance, comorbidities, and physician assessment.

Nintedanib Eugia should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product in a dry place and avoid exposure to excessive heat or humidity to maintain stability.

Nintedanib Eugia is administered orally, usually as whole tablets or capsules swallowed with water. It can be taken with or without food, but consistent intake with respect to meals helps maintain stable absorption. Patients should follow the prescribing clinician’s instructions regarding timing and any dietary considerations.

Serious risks include severe liver injury, major bleeding events, cardiovascular complications such as myocardial infarction or stroke, gastrointestinal perforation, and life‑threatening infections. Patients should report signs of jaundice, unusual bruising, chest pain, severe abdominal pain, or fever promptly to their healthcare provider.

Nintedanib is contraindicated in patients with known hypersensitivity to the active substance or any excipients, those with active severe hepatic impairment, and individuals with uncontrolled bleeding disorders. Caution is also advised for patients with severe renal dysfunction, recent major cardiovascular events, or who are pregnant or breastfeeding.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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