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:
EG000
Title:
Open-label (OL) Adalimumab (Period 1), Full Analysis Set
Description:
40 mg every other week (eow), Weeks 0-28. The Full Analysis Set included all participants who enrolled in the open-label period (Period 1) and received at least 1 dose of adalimumab.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
673
Other Number Affected:
221
Other Number At Risk:
673
Study:
NCT01808118
Results Section:
NCT01808118
Adverse Events Module:
NCT01808118