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 @ 4:50 AM
Ignite Modification Date:
2025-12-26 @ 3:51 AM
NCT ID:
NCT00843518
Group ID:
EG004
Title:
LY451395 Post-Study
Description:
The 30-day period after a participant had taken the last dose of study drug, during which time serious adverse event (SAE) information was collected.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
63
Other Number Affected:
0
Other Number At Risk:
63
Study:
NCT00843518
Results Section:
NCT00843518
Adverse Events Module:
NCT00843518