Product image of Nipfilan (Nintedanib) supplied by GNH India

Nipfilan

Active Ingredient:
Nintedanib
Origin:
EU

Nipfilan (Nintedanib)

Nintedanib, the active ingredient in Nipfilan, is a tyrosine kinase inhibitor presented as an oral formulation for oral use. It is indicated for idiopathic pulmonary fibrosis and systemic sclerosis‑associated interstitial lung disease in adult patients.

GNH India supplies Nipfilan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

G.L. Pharma Gmbh

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Indications & Clinical Uses

  • Nipfilan belongs to the tyrosine kinase inhibitor class and is used to treat fibrotic lung conditions.
  • Idiopathic pulmonary fibrosis (IPF): slows disease progression and reduces decline in lung function.
  • Systemic sclerosis‑associated interstitial lung disease (SSc‑ILD): improves lung capacity and delays fibrosis.
  • Progressive fibrosing interstitial lung disease (PF‑ILD): helps preserve lung function across multiple fibrotic subtypes.

How It Works

  • Nintedanib blocks the intracellular kinase activity of several receptor tyrosine kinases, including VEGFR, PDGFR and FGFR. By inhibiting these pathways it reduces fibroblast proliferation, angiogenesis and extracellular matrix deposition, thereby limiting the development of fibrotic tissue in the lungs.

Side Effects

Nipfilan may cause a range of adverse reactions.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Diarrhea: frequent loose stools.
  • Abdominal pain: cramping or discomfort.
  • Decreased appetite: reduced desire to eat.
  • Vomiting: occasional expulsion of stomach contents.
  • Weight loss: unintended loss of body weight.

Serious or Rare Side Effects

  • Elevated liver enzymes: potential liver injury.
  • Bleeding events: increased risk of gastrointestinal or other bleeding.
  • Cardiovascular events: possible heart failure or ischemic events.
  • Severe infections: opportunistic or serious bacterial infections.
  • Gastrointestinal perforation: rare but life‑threatening ulceration.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

  • Before initiating therapy, clinicians should evaluate several safety parameters.
  • Monitor liver function: perform baseline and periodic hepatic enzyme tests.
  • Assess cardiovascular risk: consider history of heart disease before use.
  • Evaluate bleeding risk: avoid in patients with active ulcers or on strong anticoagulants.
  • Counsel on gastrointestinal symptoms: advise patients to report persistent nausea or diarrhea.
  • Avoid in severe hepatic impairment: contraindicated when liver function is markedly compromised.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nipfilan can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce effectiveness.
  • NSAIDs (e.g., ibuprofen, naproxen): increase gastrointestinal toxicity.
  • Statins (e.g., simvastatin, atorvastatin): potential for increased statin levels.

Frequently Asked Questions

Nipfilan contains nintedanib and is approved for the treatment of idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and other progressive fibrosing interstitial lung diseases. In these conditions it helps slow the decline of lung function and reduces the formation of scar tissue.

Nintedanib inhibits multiple receptor tyrosine kinases—VEGFR, PDGFR and FGFR—blocking signals that drive fibroblast growth, new blood‑vessel formation and extracellular matrix production. By disrupting these pathways, the drug limits the development and progression of fibrotic tissue in the lungs.

The exact dose of Nipfilan is determined by the prescribing physician based on the patient’s clinical condition, weight, renal and hepatic function, and other medications. Dosage adjustments are made according to the prescriber’s assessment and local labeling.

Safety data for nintedanib in pregnancy and lactation are limited. The product should only be used if the potential benefit justifies the potential risk to the fetus or infant, and it is generally avoided unless specifically advised by a qualified healthcare professional.

To request Nipfilan, 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.

Nipfilan (nintedanib) and pirfenidone are the two main antifibrotic agents approved for idiopathic pulmonary fibrosis. Nintedanib targets multiple tyrosine kinases, while pirfenidone has a different anti‑inflammatory and anti‑oxidant mechanism. Choice of therapy depends on patient tolerance, comorbidities and physician preference.

Nipfilan should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, heat and direct sunlight to maintain stability and potency throughout its shelf life.

Nipfilan is taken orally, usually as a tablet, with food to reduce gastrointestinal upset. The exact dosing schedule is set by the prescribing clinician, who will also advise on any necessary dose adjustments based on tolerability and clinical response.

The most serious risks include liver enzyme elevations that may indicate hepatic injury, severe bleeding events, cardiovascular complications such as heart failure, and rare but life‑threatening gastrointestinal perforations. Patients should be monitored regularly for these adverse outcomes.

Nipfilan is contraindicated in patients with severe hepatic impairment, uncontrolled bleeding disorders, or known hypersensitivity to nintedanib or any of its excipients. Caution is also advised for individuals with significant cardiovascular disease or those taking strong CYP3A4 inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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