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 |
|---|---|---|---|---|---|---|---|---|
| Healthy Behaviors-Daughters | General health education, activities General Health education, activities: Intervention focuses on information regarding general health knowledge and healthy behaviors (not including sex). | 0 | None | 0 | 59 | 0 | 59 | View |
| Risky Sex Prevention-Daughters | education, activities, empowerment, racial pride building Education, activities, empowerment, racial pride building: Intervention focuses on information aimed toward reducing or preventing risky sex behaviors of minority adolescent females. | 0 | None | 0 | 51 | 0 | 51 | View |
| Risky Sex Prevention-Mothers | Activities, empowerment | 0 | None | 0 | 48 | 0 | 48 | View |
| Healthy Behaviors-Mothers | General health education, activities | 0 | None | 0 | 54 | 0 | 54 | View |