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 @ 12:33 PM
Ignite Modification Date:
2025-12-25 @ 12:10 PM
NCT ID:
NCT03277261
Group ID:
EG001
Title:
Teriflunomide + IV Placebo
Description:
Participants were administered teriflunomide 14 mg tablet, orally, QD from Day 1 up to the last day of Week 95 along with the placebo IV infusion on Days 1, 15, 168, 336 and 504 (Week 72).
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
275
Other Number Affected:
181
Other Number At Risk:
275
Study:
NCT03277261
Results Section:
NCT03277261
Adverse Events Module:
NCT03277261