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 @ 3:52 AM
Ignite Modification Date:
2025-12-26 @ 2:41 AM
NCT ID:
NCT00129402
Group ID:
EG002
Title:
Long-term Coadministration of Ezetimibe With Simvastatin
Description:
Column 3 provides the combined AE data collected for
all subjects that participated during Period 3. One subject who entered Period 3 did not receive study medication and was not included in the analysis.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
227
Other Number Affected:
42
Other Number At Risk:
227
Study:
NCT00129402
Results Section:
NCT00129402
Adverse Events Module:
NCT00129402