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 @ 2:50 AM
Ignite Modification Date:
2025-12-26 @ 1:32 AM
NCT ID:
NCT01464333
Group ID:
EG000
Title:
Humira
Description:
Participants who were prescribed Humira per approved prescribing information of Humira in Japan.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
58
Serious Number At Risk:
389
Other Number Affected:
104
Other Number At Risk:
389
Study:
NCT01464333
Results Section:
NCT01464333
Adverse Events Module:
NCT01464333