Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 11:28 PM
Ignite Modification Date:
2025-12-25 @ 9:15 PM
NCT ID:
NCT04583956
Group ID:
EG000
Title:
Remdesivir + Risankizumab
Description:
200-mg intravenous (IV) remdesivir loading dose on Day 1, followed by a 100-mg once-daily IV maintenance dose up to a 10-day total course while hospitalized and 1200-mg IV risankizumab infusion (300-mg x 4 vials) once on Day 1.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
24
Serious Number At Risk:
100
Other Number Affected:
24
Other Number At Risk:
100
Study:
NCT04583956
Results Section:
NCT04583956
Adverse Events Module:
NCT04583956