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:
2025-12-25 @ 2:47 AM
Ignite Modification Date:
2025-12-26 @ 1:27 AM
NCT ID:
NCT03370133
Group ID:
EG001
Title:
Bimekizumab 320 mg Q4W Initial Period (SS)
Description:
During the 16-week Initial Treatment Period participants received bimekizumab 320 mg Q4W. Participants formed the SS.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
5
Serious Number At Risk:
321
Other Number Affected:
87
Other Number At Risk:
321
Study:
NCT03370133
Results Section:
NCT03370133
Adverse Events Module:
NCT03370133