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 @ 1:46 AM
Ignite Modification Date:
2025-12-26 @ 12:04 AM
NCT ID:
NCT03269994
Group ID:
EG000
Title:
Cefoxitin
Description:
Participants will receive one dose of cefoxitin within 1 hour of incision time, redosed every 2-4 hours in the operating room until closure of the incision, and discontinued within 24 hours after anesthesia end time.
Deaths Number Affected:
10
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
400
Other Number Affected:
0
Other Number At Risk:
400
Study:
NCT03269994
Results Section:
NCT03269994
Adverse Events Module:
NCT03269994