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 @ 7:33 PM
Ignite Modification Date:
2025-12-25 @ 5:15 PM
NCT ID:
NCT01789203
Group ID:
EG000
Title:
Ciprofloxacin
Description:
Ciprofloxacin will be administered as two-250 mg capsules, administered once daily for 3 months post-transplant
Ciprofloxacin: Patients will be randomized 2:1 active comparator to placebo comparator.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
35
Serious Number At Risk:
133
Other Number Affected:
108
Other Number At Risk:
133
Study:
NCT01789203
Results Section:
NCT01789203
Adverse Events Module:
NCT01789203