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

135 drugs 94 manufacturers

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Drugs that treat it

Common Idiopathic pulmonary fibrosis therapies.

Showing 91–99 of 135 drugs

PREDNISONE

GLUCOCORTICOSTEROIDS·PULMONARY TUBERCULOSIS·+67
CAMBRIDGE THERA

PREDNISONE

GLUCOCORTICOSTEROIDS·PULMONARY TUBERCULOSIS·+67
DENTON PHARMA I

PREDNISONE

GLUCOCORTICOSTEROIDS·PULMONARY TUBERCULOSIS·+67
APHENA PHARMA S

PIRFENIDONE

PULMONARY FIBROSIS TREATMENT AGENTS - ANTIFIBROTIC THERAPY·IDIOPATHIC PULMONARY FIBROSIS
NOVADOZ PHARMAC

PIRFENIDONE

PULMONARY FIBROSIS TREATMENT AGENTS - ANTIFIBROTIC THERAPY·IDIOPATHIC PULMONARY FIBROSIS
EXELAN PHARMACE

PIRFENIDONE

PULMONARY FIBROSIS TREATMENT AGENTS - ANTIFIBROTIC THERAPY·IDIOPATHIC PULMONARY FIBROSIS
TEVA USA

PREDNISONE

GLUCOCORTICOSTEROIDS·PULMONARY TUBERCULOSIS·+67
PD-RX PHARM

PREDNISONE

GLUCOCORTICOSTEROIDS·PULMONARY TUBERCULOSIS·+67
AHP
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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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