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Its rapidly broken down in the liver into amino acids and excreted through urine and bile

doi: 10.1002/jsfa.903 CrossRef Full Text | Google Scholar Briat, J.-F., Gojon, A., Plassard, C., Rouached, H., and Lemaire, G

[3] Currently, a diagnosis of IPF requires: Exclusion of known causes of interstitial lung disease (ILD), e.g., domestic and occupational environmental exposures, connective tissue disorders, or drug exposure/toxicity The presence of a typical radiological pattern of usual interstitial pneumonia (UIP) on high-resolution computed tomography (HRCT)