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 @ 4:33 AM
Ignite Modification Date:
2025-12-26 @ 3:35 AM
NCT ID:
NCT01698918
Group ID:
EG001
Title:
Everolimus+Exemestane (Second-line On-treatment)
Description:
AEs during second-line on-treatment period were collected from first second-line dose to 28 days post second-line treatment
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
8
Serious Number At Risk:
53
Other Number Affected:
43
Other Number At Risk:
53
Study:
NCT01698918
Results Section:
NCT01698918
Adverse Events Module:
NCT01698918