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 @ 4:28 AM
Ignite Modification Date:
2025-12-26 @ 3:31 AM
NCT ID:
NCT00686920
Group ID:
EG000
Title:
New Rifaximin
Description:
Participants new to receiving rifaximin were administered a single rifaximin 550 milligram (mg) tablet 2 times per day (approximately every 12 hours) for at least 24 months, until regulatory approval of rifaximin for reduction in risk of overt HE recurrence, or until the sponsor closed the study.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
158
Serious Number At Risk:
252
Other Number Affected:
212
Other Number At Risk:
252
Study:
NCT00686920
Results Section:
NCT00686920
Adverse Events Module:
NCT00686920