Table 4

Side effects

ParametersAllBoceprevirTelaprevirp-Value
n=23n=8n=15
Fatigue20 (87)7 (87.5)13 (86.7)1
Depression5 (21.7)05 (33.3)0.12
Nausea5 (21.7)2 (25)3 (20)1
Skin or subcutaneous tissue disorder
 Toxic skin eruption1
  Grade 11 (4.3)01 (6.6)
  Grade 21 (4.3)01 (6.6)
 Pruritus9 (39.1)2 (25)7 (46.6)0.4
Haematologic variables
 Decreased haemoglobin concentration0.22
  Grade 1: 9.5–10.9 g/dl3 (13)1 (12.5)2 (13.3)
  Grade 2: 8.0–9.4 g/dl11 (47.8)2 (25)9 (60)
  Grade 3: 6.5–7.9 g/dl3 (13)1 (12.5)2 (13.3)
  Grade 4: <6.5 g/dl000
  Erythropoietin use20 (87)7 (87.5)13 (86.6)1
  Red-cell transfusion9 (39.1)2 (25)7 (46.6)0.4
 Decreased absolute neutrophil count0.56
  Grade 1: 1500–1900/mm32 (8.7)02 (13.3)
  Grade 2: 1000–1400/mm38 (34.8)4 (50)4 (26.6)
  Grade 3: 500–1000/mm38 (34.8)3 (37.5)5 (33.3)
  Grade 4: <500/mm32 (8.7)1 (12.5)1 (6.6)
  Use of granulocyte-stimulating agent2 (8.7)1 (12.5)1 (6.6)1
 Decreased platelet count0.59
  Grade 1: 75000–99000/mm33 (13)03 (20)
  Grade 2: 50000–74000/mm38 (34.8)3 (37.5)5 (33.3)
  Grade 3: 25000–49000/mm34 (17.4)1 (12.5)3 (20)
  Grade 4:<25000/mm3000
Infection11 (47.8)3 (37.5)8 (53.3)0.67
 Urinary tract3 (13)2 (25)1 (6.6)
 Pneumopathy3 (13)1 (12.5)2 (13.3)
 Cholecystitis1 (4.3)01 (6.6)
 Dental abscess1 (4.3)01 (6.6)
 Breast abscess1 (4.3)01 (6.6)
 Otitis1 (4.3)01 (6.6)
Reason for discontinuation
 Virological non-response5 (21.7)3 (37.5)2 (13.3)
 Virological relapse2 (8.7)02 (13.3)
 Depression1 (4.3)1 (12.5)0
  • Except where indicated otherwise values are n (%).