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 @ 6:45 PM
Ignite Modification Date:
2025-12-25 @ 4:17 PM
NCT ID:
NCT01721057
Group ID:
EG002
Title:
Baricitinib 4 Mg-Treatment Period
Description:
Baricitinib 4 mg administered orally once daily through Week 24.
Participants continued to take background cDMARD therapy throughout study.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
12
Serious Number At Risk:
227
Other Number Affected:
127
Other Number At Risk:
227
Study:
NCT01721057
Results Section:
NCT01721057
Adverse Events Module:
NCT01721057