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 @ 1:08 AM
Ignite Modification Date:
2025-12-25 @ 11:20 PM
NCT ID:
NCT04054193
Group ID:
EG001
Title:
Fosaprepitant Cycles 2-3
Description:
Participants received fosaprepitant dimeglumine once daily (QD) for 3 days and were followed for 14 days during Cycles 2-3. Participants also optionally received dexamethasone as background therapy, and a 5-HT3 receptor antagonist on Day 1 and optionally on Days 2-3 as background therapy, of each 17-day cycle.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
27
Serious Number At Risk:
69
Other Number Affected:
27
Other Number At Risk:
69
Study:
NCT04054193
Results Section:
NCT04054193
Adverse Events Module:
NCT04054193