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Frequency of adverse events during the study period (efficacy population)
| Adverse events reported by ≥5% of patients, n (%) | n = 53 |
| Insomnia | 12 (22.6) |
| Increased prolactin | 9 (17.0) |
| Weight gain | 7 (13.2) |
| Anxiety | 3 (5.7) |
| Epigastralgia | 3 (5.7) |
| Reduced appetite | 3 (5.7) |
| Adverse events related to the study drug, n (%) | n = 53 |
| Increased prolactin | 9 (17.0) |
| Weight gain | 5 (9.4) |
