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 @ 9:10 PM
Ignite Modification Date:
2025-12-25 @ 7:00 PM
NCT ID:
NCT01218204
Group ID:
EG004
Title:
Atorvastatin 10 mg (Part B Run-in)
Description:
After washout participants received atorvastatin 10 mg for a 4-week stabilization Run-in Period.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
62
Other Number Affected:
19
Other Number At Risk:
62
Study:
NCT01218204
Results Section:
NCT01218204
Adverse Events Module:
NCT01218204