Table 2.
Prevalence of adverse events (AEs) related to the use of direct-acting antivirals in the study group according to the participants’ age
| Symptom | All participants (n = 165) |
Young children (n = 35) |
Older children (n = 130) |
p |
|---|---|---|---|---|
| Number of children with any AE* | 74 (45%) | 16 (46%) | 58 (45%) | NS |
| Abdominal pain | 17 (10%) | 6 (17%) | 9 (7%) | NS |
| Fatigue/asthenia | 16 (10%) | 1 (3%) | 15 (12%) | NS |
| Headache | 14 (8%) | 0 | 14 (11%) | 0.04 |
| Diarrhea | 10 (6%) | 3 (9%) | 7 (5%) | NS |
| Somnolence | 9 (5%) | 0 | 9 (7%) | NS |
| Pruritus | 7 (4%) | 2 (6%) | 5 (4%) | NS |
| Vomiting | 7 (4%) | 3 (9%) | 4 (3%) | NS |
| Rash | 7 (4%) | 3 (9%) | 4 (3%) | NS |
| Nausea | 3 (2%) | 0 | 3 (2%) | NS |
| Dizziness | 3 (2%) | 0 | 3 (2%) | NS |
| Epistaxis | 3 (2%) | 2 (6%) | 1 (1%) | NS |
| Other** | 7 (4%) | 0 | 7 (5%) | NS |
*There were children who reported more than one AE
NS nonsignificant (p ≥ 0.05)
**Include the following AEs that occurred in no more than two children: syncope, hair loss, calf cramps, abnormal taste, and chest pain