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 @ 4:54 AM
Ignite Modification Date:
2025-12-26 @ 3:55 AM
NCT ID:
NCT02437318
Group ID:
EG001
Title:
Placebo + Fulvestrant
Description:
All-cause mortality from randomization until 30 days after last dose. Adverse Events from first dose until 30 days after last dose.
Deaths Number Affected:
12
Deaths Number At Risk:
None
Serious Number Affected:
54
Serious Number At Risk:
287
Other Number Affected:
244
Other Number At Risk:
287
Study:
NCT02437318
Results Section:
NCT02437318
Adverse Events Module:
NCT02437318