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 @ 3:25 AM
Ignite Modification Date:
2025-12-26 @ 2:05 AM
NCT ID:
NCT01431105
Group ID:
EG000
Title:
Atorvasatin
Description:
Atorvastatin dose titration to maximum tolerated dose
Atorvastatin: Atorvastatin dose titration to maximum tolerated dose (once daily for 6 weeks)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
34
Other Number Affected:
24
Other Number At Risk:
34
Study:
NCT01431105
Results Section:
NCT01431105
Adverse Events Module:
NCT01431105