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:
EG000
Title:
Everolimus+Letrozole (First-line on Treatment)
Description:
AEs during first-line on-treatment period were collected from the initial first-line dose to 28 days after the last first-line dose, for participants without second-line. For those with second-line treatment, the period lasts until the minimum of 28 days after the last first-line dose or one day before second-line treatment administration.
Deaths Number Affected:
11
Deaths Number At Risk:
None
Serious Number Affected:
72
Serious Number At Risk:
202
Other Number Affected:
202
Other Number At Risk:
202
Study:
NCT01698918
Results Section:
NCT01698918
Adverse Events Module:
NCT01698918