Table 3

 Adverse events reported by patients in the three groups who received peginterferon alpha-2b plus ribavirin for 24, 36, or 48 weeks

Adverse eventGroup A (24 weeks) (n = 95)Group B (36 weeks) (n = 96)Group C (48 weeks) (n = 96)
Fatigue56 (60)59 (64)62 (66)
Influenza-like illness53 (57)58 (63)59 (63)
Headache49 (53)52 (57)58 (62)
Myalgia48 (52)52 (57)58 (62)
Pyrexia41 (44)50 (54)53 (62)
Insomnia31(33)35 (38)46 (49)
Injection site erythema28 (30)34 (37)39 (42)
Irritability26 (28)33 (36)30 (32)
Back pain23 (25)25 (27)29 (31)
Rigors16 (17)17 (18)21 (22)
Sore throat13 (14)16 (17)20 (21)
Cough12 (13)15 (16)20 (21)
Pruritus10 (11)15 (16)18 (19)
Anorexia9 (10)14 (15)18 (19)
Arthralgia8 (9)12 (13)17 (18)
Dyspnoea8 (9)11 (12)15 (16)
Rash7 (8)10 (11)12 (13)
Depression3 (3)3 (3)9 (9)
Dry mouth5 (5)7 (8)8 (9)
Alopecia4 (4)6 (7)7 (7)
Nausea4 (4)4 (4)7 (7)
Dizziness3 (3)5 (5)6 (6)
Abdominal pain3 (3)5 (5)7 (7)
Dry skin2 (2)6 (7)7 (7)
Diarrhoea2 (2)6 (7)8 (9)
Vomiting1 (2)3 (3)5 (5)
Discontinuation of therapy (n (%))
    Haematological abnormalities1 (2)2 (2)
    Psychiatric003 (3)
    Hypothyroidism001 (1)
Reduction or omission of 1–2 doses for adverse events or laboratory abnormalities
    PEG-IFN-α-2b5 (5)11 (12)12 (13)
    Ribavirin9 (10)13 (14)18 (19)