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 @ 12:00 AM
Ignite Modification Date:
2025-12-25 @ 9:58 PM
NCT ID:
NCT00871858
Group ID:
EG001
Title:
Arm B (FULV)
Description:
Patients receive fulvestrant intramuscularly ( 250 mg/5 ml solution) on days 1, 14, and 28 and then once a month thereafter until 6 months.
fulvestrant: Given intramuscularly
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
58
Other Number Affected:
43
Other Number At Risk:
58
Study:
NCT00871858
Results Section:
NCT00871858
Adverse Events Module:
NCT00871858