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Table 2 Tolerability and adverse drug reactions (ADRs) of pirfenidone therapy

From: A multicentre retrospective observational study on Polish experience of pirfenidone therapy in patients with idiopathic pulmonary fibrosis: the PolExPIR study

Full dose treatment, n (%)

272 (88.6)

Different than full dose treatment, n (%)

35 (11.4)

Intermittent drug interruption and/or reduction of dosing, n (%)

74 (24.1)

ADRs

 Nausea, n (%)

75 (24.43)

 Decreased appetite, n (%)

105 (34.2)

 Diarrhoea, n (%)

33 (10.75)

 Vomiting, n (%)

15 (4.89)

 Dyspepsia, n (%)

71 (23.13)

 Loss of weight, n (%)

100 (32.57)

 Cough, n (%)

88 (28.66)

 Fatigue, n (%)

110 (35.83)

 Dizziness, n (%)

42 (13.68)

 Skin rash, n (%)

58 (18.89)

 Photosensitivity, n (%)

54 (17.59)

 Elevated liver enzymes, n (%)

9 (2.93)

 Sleep disturbances, n (%)

49 (15.96)

 Other, n (%)

36 (11.73)

  1. Abbreviations: ADRs adverse drug reactions