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 @ 7:02 PM
Ignite Modification Date:
2025-12-25 @ 4:35 PM
NCT ID:
NCT05584657
Group ID:
EG000
Title:
Sulopenem Etzadroxil/Probenecid
Description:
Sulopenem etzadroxil/probenecid 500 mg/500 mg PO twice daily for 5 days
Sulopenem etzadroxil/probenecid: Oral sulopenem twice daily for 5 days
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
1107
Other Number Affected:
198
Other Number At Risk:
1107
Study:
NCT05584657
Results Section:
NCT05584657
Adverse Events Module:
NCT05584657