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Number of subjects who experienced adverse events, regardless of study drug relationship (safety population, N=22)
| Adverse event, n (%) | All subjects (N=22) |
|---|---|
| Total | 12 (54.5) |
| Headache | 6 (27.3) |
| Dry skin | 2 (9.1) |
| Myalgia | 2 (9.1) |
| Nasopharyngitis | 2 (9.1) |
| Nausea | 2 (9.1) |
| Diarrhea | 1 (4.5) |
| Dizziness | 1 (4.5) |
| Erythema | 1 (4.5) |
| Oral herpes | 1 (4.5) |
| Phlebitis | 1 (4.5) |
| Rhinitis | 1 (4.5) |
| Vaginal hemorrhage | 1 (4.5) |
| Vomiting | 1 (4.5) |
Note: All adverse events were grade 1 or 2.
