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Adverse Events (Treated Set)
| n (%) | Child‐Pugh A (n = 8) | Child‐Pugh B (n = 8) | Healthy (n = 17) |
|---|---|---|---|
| Subjects with any AE | 0 | 3 (37.5) | 3 (17.6) |
| Headache | 0 | 0 | 1 (5.9) |
| Diarrhea | 0 | 1 (12.5) | 0 |
| Nausea | 0 | 1 (12.5) | 2 (11.8) |
| Vomiting | 0 | 0 | 1 (5.9) |
| Pruritus | 0 | 1 (12.5) | 0 |
| Skin irritation | 0 | 1 (12.5) | 0 |
Adverse events (AEs) were reported according to MedDRA version 17.1. AEs with onset between administration of trial medication and the end of the 28‐day posttreatment follow‐up period are shown.
