Table 3.
Reported adverse events (Part B).
| Distinct subjects [n (%)] | |||||
|---|---|---|---|---|---|
| Adverse event | Placebo (n = 12) | 250 mg (n = 12) | 500 mg (n = 12) | 1000 mg (n = 12) | Overall (n = 12) |
| Euphoric mood | 0 (0.0%) | 3 (25.0%) | 6 (50.0%) | 7 (58.3%) | 10 (83.3%) |
| Dizziness | 1 (8.3%) | 1 (8.3%) | 4 (33.3%) | 6 (50.0%) | 9 (75.0%) |
| Somnolence | 2 (16.7%) | 3 (25.0%) | 3 (25.0%) | 3 (25.0%) | 6 (50.0%) |
| Headache | 2 (16.7%) | 0 (0.0%) | 0 (0.0%) | 0 (0.0%) | 2 (16.7%) |
| Nausea | 0 (0.0%) | 0 (0.0%) | 0 (0.0%) | 1 (8.3%) | 1 (8.3%) |
| Pharyngitis | 0 (0.0%) | 0 (0.0%) | 0 (0.0%) | 1 (8.3%) | 1 (8.3%) |
| Muscle spasms | 0 (0.0%) | 0 (0.0%) | 0 (0.0%) | 1 (8.3%) | 1 (8.3%) |
| Rhinorrhea | 0 (0.0%) | 0 (0.0%) | 1 (8.3%) | 0 (0.0%) | 1 (8.3%) |
| Contact dermatitis | 0 (0.0%) | 0 (0.0%) | 1 (8.3%) | 1 (8.3%) | 1 (8.3%) |