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 @ 1:40 AM
Ignite Modification Date:
2025-12-25 @ 11:57 PM
NCT ID:
NCT01954394
Group ID:
EG002
Title:
Alirocumab: All Participants
Description:
All participants who received alirocumab/placebo in the parent studies and received alirocumab 75 mg or 150 mg SC injection Q2W added to stable LMT for up to 168 weeks in this study.
Deaths Number Affected:
11
Deaths Number At Risk:
None
Serious Number Affected:
212
Serious Number At Risk:
985
Other Number Affected:
549
Other Number At Risk:
985
Study:
NCT01954394
Results Section:
NCT01954394
Adverse Events Module:
NCT01954394