Table 6.
Placebo (n = 63) | Ato75 (n = 63) | AD109 2.5/75 mg (n = 42) | AD109 5/75 mg (n = 41) | |
---|---|---|---|---|
Any adverse event | 25 (39.7%) | 51 (81%) | 26 (61.9%) | 32 (78%) |
Adverse event leading to discontinuation | 1 (2%) | 12 (19%) | 5 (12%) | 5 (12%) |
Most common adverse events* | ||||
Dry mouth | 3 (5%) | 17 (27%) | 10 (24%) | 24 (59%) |
Insomnia | 2 (3%) | 23 (37%) | 11 (26%) | 9 (22%) |
Urinary hesitation/flow decrease | 0 | 14 (22%) | 3 (7%) | 9 (22%) |
Constipation | 2 (3%) | 2 (3%) | 0 | 5 (12%) |
Nausea | 2 (3%) | 4 (6%) | 5 (12%) | 4 (10%) |
Decreased appetite | 1 (2%) | 5 (8%) | 2 (5%) | 4 (10%) |
Feeling jittery | 1 (2%) | 2 (3%) | 2 (5%) | 3 (7%) |
Somnolence | 1 (2%) | 0 | 1 (2%) | 3 (7%) |
Definition of abbreviation: Ato75 = atomoxetine 75 mg.
Most common adverse events are those reported in at least three participants in any treatment group.