Indication

Idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis is a specific, chronic, and progressive fibrosing interstitial lung disease of unknown etiology that is limited to the respiratory system. Read more about Idiopathic pulmonary fibrosis

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Drugs that treat it

Common Idiopathic pulmonary fibrosis therapies.

Showing 19–27 of 135 drugs

OFEV (nintedanib esylate)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·SYSTEMIC SCLEROSIS-ASSOCIATED INTERSTITIAL LUNG DISEASE·+2
Boehringer Ingelheim
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About Idiopathic pulmonary fibrosis.

Idiopathic pulmonary fibrosis is a specific, chronic, and progressive fibrosing interstitial lung disease of unknown etiology that is limited to the respiratory system.

It primarily occurs in older adults, typically presenting in individuals over 50 to 60 years of age, and has a slight male predominance.

Pathophysiologically, repetitive micro-injury to the alveolar epithelium triggers aberrant wound healing, progressive fibroblast proliferation, and excessive extracellular matrix deposition, culminating in the destruction of normal lung architecture and a hallmark radiological or histopathological pattern of usual interstitial pneumonia.

Clinically, affected patients develop worsening exertional dyspnea, an intractable nonproductive cough, bibasilar inspiratory crackles, digital clubbing, and restrictive ventilatory impairment that often leads to respiratory failure.

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