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 @ 3:21 AM
Ignite Modification Date:
2025-12-26 @ 1:59 AM
NCT ID:
NCT00535405
Group ID:
EG001
Title:
Ezetimibe 10 mg/Simvastatin 20 mg
Description:
Ezetimibe (EZ) 10 mg/simvastatin (Simva) 20 mg once daily for 12 weeks
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
8
Serious Number At Risk:
256
Other Number Affected:
32
Other Number At Risk:
256
Study:
NCT00535405
Results Section:
NCT00535405
Adverse Events Module:
NCT00535405