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Overall rates of adverse events in Studies 1 and 2.
| Placebo | OnabotA 240 U |
OnabotA 360 U |
|
|---|---|---|---|
| Number (%) of Patients | |||
| Study 1 | |||
| Any AEs | 28/36 (77.8%) | 22/36 (61.1%) | 26/36 (72.2%) |
| Treatment-related AEs | 5/36 (13.9%) | 6/36 (16.7%) | 5/36 (13.9%) |
| Serious AEs | 3/36 (8.3%) | 1/36 (2.8%) | 3/36 (8.3%) |
| Study 2 | |||
| Any AEs | 25/48 (52.1%) | 30/52 (57.7%) | 28/55 (50.9%) |
| Treatment-related AEs | 4/48 (8.3%) | 5/52 (9.6%) | 7/55 (12.7%) |
| Serious AEs | 7/48 (14.6%) | 9/52 (17.3%) | 6/55 (10.9%) |
AE = adverse event.
