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 @ 1:16 PM
Ignite Modification Date:
2025-12-25 @ 12:24 PM
NCT ID:
NCT02714595
Group ID:
EG000
Title:
Cefiderocol
Description:
Participants received 2 g cefiderocol administered intravenously over 3 hours, every 8 hours for 7-14 days.
Deaths Number Affected:
34
Deaths Number At Risk:
None
Serious Number Affected:
50
Serious Number At Risk:
101
Other Number Affected:
88
Other Number At Risk:
101
Study:
NCT02714595
Results Section:
NCT02714595
Adverse Events Module:
NCT02714595