Table 4.
Percentage of subjects for each treatment group reporting adverse events
| Adverse event | Quetiapine (%, n) | Placebo (%, n) |
| Sedation | 75% (15) | 33.3%(7) |
| Dry mouth | 15% (3) | 0 |
| Headache | 15% (3) | 38% (8) |
| Fatigue | 15% (3) | 19% (4) |
| Irritability | 10% (2) | 4.7% (1) |
| Impaired concentration | 10% (2) | 0 |
| Dizziness | 5% (1) | 14.3% (3) |
| Nausea | 5% (1) | 9.5% (2) |
| Increased appetite | 5% (1) | 9.5% (2) |
| Delayed ejaculation | 5% (1) | 0 |
| Weight gain | 5% (1) | 0 |
| Worsening mood | 5%(1) | 4.7%(1) |
| Memory difficulties | 5%(1) | 0 |
| Muscle aches | 5%(1) | 0 |
| Abdominal tenderness | 5%(1) | 0 |
| Slurred speech | 5%(1) | 0 |