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 |
|---|---|---|---|---|---|---|---|---|
| Pooled Placebo | Participants received placebo matched to 550 mg or 1100 mg AT-527 twice a day (BID) on Days 1-5. | 0 | None | 1 | 40 | 1 | 40 | View |
| AT-527 550 mg (1x550 mg) | Participants received 550 mg AT-527 (1x550 mg) twice a day (BID) on Days 1-5. | 0 | None | 1 | 30 | 1 | 30 | View |
| AT-527 1100 mg (4x275 mg) | Participants received 1100 mg AT-527 (4x275 mg) twice a day (BID) on Days 1-5. | 0 | None | 1 | 30 | 5 | 30 | View |