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 @ 4:48 AM
Ignite Modification Date:
2025-12-26 @ 3:50 AM
NCT ID:
NCT01854918
Group ID:
EG003
Title:
Years 2-3: Evolocumab + SOC / Evolocumab + SOC
Description:
Participants continued to receive evolocumab plus SOC for approximately 2 years during the all-IP period. Evolocumab was administered at a dose of 140 mg Q2W or 420 mg QM based on participant choice.
Deaths Number Affected:
16
Deaths Number At Risk:
None
Serious Number Affected:
344
Serious Number At Risk:
2391
Other Number Affected:
928
Other Number At Risk:
2391
Study:
NCT01854918
Results Section:
NCT01854918
Adverse Events Module:
NCT01854918