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 |
|---|---|---|---|---|---|---|---|---|
| Methylene Blue MMX® 200mg | Oral dose, 8 Methylene Blue MMX® tablets over a 4hr schedule Methylene Blue MMX® | None | None | 1 | 485 | 234 | 488 | View |
| Methylene Blue MMX® 100mg | Oral dose, 4 Methylene Blue MMX® tablets and 4 Placebo tablets over a 4hr schedule Methylene Blue MMX® Placebo: Sugar pill manufactured to mimic Methylene Blue MMX® tablet. | None | None | 1 | 241 | 102 | 241 | View |
| Placebo | Oral dose, 8 Placebo tablets over a 4hr schedule Placebo: Sugar pill manufactured to mimic Methylene Blue MMX® tablet. | None | None | 0 | 479 | 7 | 479 | View |