Table 3 Subjects experiencing at least one adverse event likely due to study treatment, by study arm
Experienced an adverse event | Randomised Group | ||
|---|---|---|---|
Intervention | Standard | Total | |
No | 23 | 20 | 43 |
Yes | 4 (14.8%) | 5 (20.0%) | 9 |
Total | 27 | 25 | 52 |
Experienced an adverse event | Randomised Group | ||
|---|---|---|---|
Intervention | Standard | Total | |
No | 23 | 20 | 43 |
Yes | 4 (14.8%) | 5 (20.0%) | 9 |
Total | 27 | 25 | 52 |