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 @ 6:54 PM
Ignite Modification Date:
2025-12-25 @ 4:27 PM
NCT ID:
NCT01212757
Group ID:
EG005
Title:
APR Exposure Period Up to 5 Years: APR 30 mg
Description:
Participants who received 30 mg apremilast twice daily regardless of when their apremilast-exposure started (at Weeks 0, 16, or 24).
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
41
Serious Number At Risk:
234
Other Number Affected:
166
Other Number At Risk:
234
Study:
NCT01212757
Results Section:
NCT01212757
Adverse Events Module:
NCT01212757