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 @ 3:48 AM
Ignite Modification Date:
2025-12-26 @ 2:36 AM
NCT ID:
NCT02563002
Group ID:
EG000
Title:
Pembrolizumab First Course
Description:
Participants received pembrolizumab 200 mg intravenously (IV) on Day 1 of each 21-day cycle (Q3W) for up to 35 treatments (approximately 2 years).
Deaths Number Affected:
68
Deaths Number At Risk:
None
Serious Number Affected:
62
Serious Number At Risk:
153
Other Number Affected:
145
Other Number At Risk:
153
Study:
NCT02563002
Results Section:
NCT02563002
Adverse Events Module:
NCT02563002