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 @ 2:50 PM
Ignite Modification Date:
2025-12-25 @ 1:17 PM
NCT ID:
NCT01076959
Group ID:
EG000
Title:
Humira
Description:
Patients who received Humira for 24 weeks during the PMDA review period.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
469
Serious Number At Risk:
7740
Other Number Affected:
863
Other Number At Risk:
7740
Study:
NCT01076959
Results Section:
NCT01076959
Adverse Events Module:
NCT01076959