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. 2012 Jan 3;7(1):e28115. doi: 10.1371/journal.pone.0028115

Table 3. Adverse events or intercurrent illness throughout treatment with weekly pegIFN-α-2a (135 µg) plus oral Ribavirin (400 mg twice daily); n = 58 patients.

Total Grade 1 -2 Grade 3 Grade 4
no. (%) no. (%) no. (%) no. (%)
Flu-like syndrome 30 (51.7) 27 (46.5) 3 (5.1)
Myalgia 9 (15.5) 8 (13.7) 1 (1.7)
Fatigue 28 (48.2) 28 (48.2)
Unintentional weight loss ≥10% 14 (24.1) 14 (24.1)
Anorexia 23 (39.6) 23 (39.6)
Depression 14 (24.1) 13 (22.4) 1 (1.7)
Irritability - nervousness 12 (20.6) 11 (18.9) 1 (1.7)
Insomnia 11 (18.9) 10 (16.7) 1 (1.7)
Nausea – vomiting 15 (25.8) 15 (25.8)
Anemia 7 (12.0) 6 (10.3) 1 (1.7)
Neutropenia 21 (36.2) 18 (31.0) 3 (5.1)
Thrombocytopenia 10 (18.3) 10 (18.3)
Other
- Subarachnoid hemorrhage (death) 1 (1.7) 1 (1.7)
- Neuroleptic malignant syndrome (death) 1 (1.7) 1 (1.7)
- Sudden death 1 (1.7) 1 (1.7)
- Pneumococcal pneumonia 1 (1.7) 1 (1.7)
- Esophageal stenosis (relapse) 1 (1.7) 1 (1.7)
- Thrush 1 (1.7) 1 (1.7)
- Deep vein thrombosis 1 (1.7) 1 (1.7)
- Cough 2 (3.4) 2 (3.4)
- Headache 2 (3.4) 2 (3.4)
- Dizziness 1 (1.7) 1 (1.7)
- Injection site erythema 1 (1.7) 1 (1.7)