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 @ 5:43 PM
Ignite Modification Date:
2025-12-25 @ 3:12 PM
NCT ID:
NCT00510068
Group ID:
EG002
Title:
Open Label - Everolimus 10mg
Description:
Afinitor OL (for data collected in the open-label period of the study): The open-label set included only patients who received at least one dose of open-label everolimus 10 mg and had at least one safety assessment during the open-label period of the study.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
108
Serious Number At Risk:
225
Other Number Affected:
218
Other Number At Risk:
225
Study:
NCT00510068
Results Section:
NCT00510068
Adverse Events Module:
NCT00510068