Serious Event
Serious Adverse Events (SAEs) are adverse events that result in death, are life-threatening, require or prolong hospitalization, cause persistent or significant disability/incapacity, or are congenital anomalies/birth defects. Each serious event is categorized by term, organ system, assessment type, and source vocabulary to provide standardized reporting across clinical trials.
Serious Event path is as follows:
Study -> Results Section -> Adverse Events Module -> Serious Event
Study -> Results Section -> Adverse Events Module -> Serious Event -> Serious Event Stats
Serious Event
Serious Event Stats
| Group ID | # Events | # Affected | # At Risk | View |
|---|---|---|---|---|
| EG000 | None | 0 | 1 | View |
| EG001 | None | 0 | 1 | View |
| EG002 | None | 0 | 3 | View |
| EG003 | None | 0 | 3 | View |
| EG004 | None | 0 | 3 | View |
| EG005 | None | 0 | 3 | View |
| EG006 | None | 0 | 3 | View |
| EG007 | None | 0 | 4 | View |
| EG008 | None | 0 | 6 | View |
| EG009 | None | 1 | 3 | View |
| EG010 | None | 0 | 11 | View |
| EG011 | None | 0 | 3 | View |
| EG012 | None | 0 | 80 | View |