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 @ 4:32 AM
Ignite Modification Date:
2025-12-26 @ 3:34 AM
NCT ID:
NCT01808118
Group ID:
EG003
Title:
Any Adalimumab Population
Description:
The Any Adalimumab Population consisted of all participants who received at least 1 dose of adalimumab any time during the study (including the open-label period, double-blind period and rescue period).
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
28
Serious Number At Risk:
673
Other Number Affected:
275
Other Number At Risk:
673
Study:
NCT01808118
Results Section:
NCT01808118
Adverse Events Module:
NCT01808118