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 @ 2:48 AM
Ignite Modification Date:
2025-12-26 @ 1:30 AM
NCT ID:
NCT01928433
Group ID:
EG001
Title:
Finafloxacin 10 Days
Description:
Finafloxacin (i.v. and oral) for a total of 10 days.
Finafloxacin 800 mg i.v. once daily
Finafloxacin 800 mg tablets (as four 200 mg tablets) once daily
Ciprofloxacin placebo i.v. two times daily
Ciprofloxacin placebo oral (as two capsules each) two times daily
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
75
Other Number Affected:
19
Other Number At Risk:
75
Study:
NCT01928433
Results Section:
NCT01928433
Adverse Events Module:
NCT01928433