Other Event
Other Adverse Events are non-serious adverse events that exceed a specific frequency threshold (typically 5% within any study arm). These events are reported to provide comprehensive safety information about all noteworthy adverse occurrences during clinical trials. Each other event is categorized by term, organ system, assessment type, and source vocabulary for standardized reporting.
Other Event path is as follows:
Study -> Results Section -> Adverse Events Module -> Other Event
Study -> Results Section -> Adverse Events Module -> Other Event -> Other Event Stats
Other Event
Other Event Stats
| Group ID | # Events | # Affected | # At Risk | View |
|---|---|---|---|---|
| EG000 | None | 1 | 16 | View |
| EG001 | None | 0 | 16 | View |
| EG002 | None | 0 | 16 | View |
| EG003 | None | 0 | 16 | View |
| EG004 | None | 1 | 193 | View |
| EG005 | None | 0 | 191 | View |
| EG006 | None | 0 | 191 | View |
| EG007 | None | 0 | 196 | View |
| EG008 | None | 2 | 209 | View |
| EG009 | None | 0 | 207 | View |
| EG010 | None | 0 | 207 | View |
| EG011 | None | 0 | 212 | View |