Adverse Events Module
For researchers submitting trial data to ClinicalTrials.gov, the Adverse Events module is one of four mandatory results sections. It requires reporting in three primary categories: All-Cause Mortality: A table tracking all deaths that occurred during the study, regardless of cause. Serious Adverse Events (SAEs): A tabular summary of events resulting in death, life-threatening conditions, hospitalization, or significant disability. Other Adverse Events: A table for non-serious events that exceed a specific frequency threshold, such as 5% within any study arm.
Adverse Events Module path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Groups
Study -> Results Section -> Adverse Events Module -> Serious Events
Study -> Results Section -> Adverse Events Module -> Other Events
Adverse Events Module
Event Groups
| Title | Description | Deaths # Affected | Deaths # At Risk | Serious # Affected | Serious # At Risk | Other # Affected | Other # At Risk | View |
|---|---|---|---|---|---|---|---|---|
| VACCINE MDD | SEASONAL INFLUENZA VACCINE (0.5ML) DELIVERED I.M. INFLUENZA VACCINE: THE PURPOSE OF THE STUDY IS TO EVALUATE THE EFFICACY OF THE SEASONAL INFLUENZA VACCINE IN PEOPLE WITH MAJOR DEPRESSIVE DISORDER | None | None | 0 | 6 | 0 | 6 | View |
| PLACEBO MDD | SALINE (0.5ML) DELIVERED I.M. NaCl-saline placebo: placebo | None | None | 0 | 0 | 0 | 0 | View |
| VACCINE HC | SEASONAL INFLUENZA VACCINE (0.5ML) DELIVERED I.M. INFLUENZA VACCINE: THE PURPOSE OF THE STUDY IS TO EVALUATE THE EFFICACY OF THE SEASONAL INFLUENZA VACCINE IN PEOPLE WITH MAJOR DEPRESSIVE DISORDER | None | None | 0 | 0 | 0 | 0 | View |
| PLACEBO HC | SALINE (0.5ML) DELIVERED I.M. NaCl-saline placebo: placebo | None | None | 0 | 0 | 0 | 0 | View |