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:
2025-12-24 @ 2:28 PM
Ignite Modification Date:
2025-12-25 @ 1:02 PM
NCT ID:
NCT01231659
Group ID:
EG000
Title:
Everolimus + Letrozole
Description:
All patients received 2 tablets (5 mg each) of Everolimus (a total of 10 mg) + 1 tablet of Letrozole (2.5 mg) daily until disease progression or as described in the protocol.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
26
Serious Number At Risk:
72
Other Number Affected:
71
Other Number At Risk:
72
Study:
NCT01231659
Results Section:
NCT01231659
Adverse Events Module:
NCT01231659