Table S1.
Adverse events (per patient), mean ± SD 14.4±3.76 | ||
---|---|---|
Adverse events requiring medical treatment (per patient), mean ± SD 2.2±2.16 | ||
| ||
Common adverse event | Patients, n (%) | Requiring medical treatment, n (%)a |
Fatigue | 24 (80) | 0 |
Rash | 22 (73.3) | 13 (59.1) |
Mood change | 22 (73.3) | 3 (13.6) |
Depression | 9 (30) | 2 (22.2) |
Irritability | 16 (53.3) | 1 (6.25) |
Pruritus | 18 (60) | 0 |
Upper respiratory tract symptoms | 16 (53.3) | 4 (25) |
Weight loss | 15 (50) | 0 |
Headache | 14 (46.7) | 0 |
Sleep disturbance | 12 (40) | 5 (41.7) |
Flu-like symptoms (non-specific) | 12 (40) | 0 |
Myalgia | 11 (36.7) | 0 |
Severe hematological adverse event | ||
Hemoglobin | ||
Hb 80–99 (gL−1) | 9 (30) | 1 (11.1) |
Hb <80 (gL−1) | 1 (3.3) | 0 |
Neutrophils | ||
0.5–0.99 (×109 L−1) | 17 (56.6) | 0 |
<0.5 (×109 L−1) | 3 (10) | 0 |
Platelets | ||
50–99 (×109 L−1) | 12 (40) | 0 |
<50 (×109 L−1) | 2 (6.7) | 1 (50) |
Serious adverse events (requiring hospital admission) | 2 (6.7) | 2 (100) |
Immune thrombocytopenic purpura | 1 (3.3) | 1 (100) |
Osteomyelitis | 1 (3.3) | 1 (100) |
Note:
Percentage of total number of patients who experienced the adverse event.
Abbreviations: Hb, hemoglobin; IFN, interferon.