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:
EG002
Title:
Weeks 0-24: Apremilast 30 mg (Placebo- Controlled Phase)
Description:
Participants received 30 mg apremilast tablets PO BID during the 24-week placebo-controlled phase.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
162
Other Number Affected:
82
Other Number At Risk:
162
Study:
NCT01212757
Results Section:
NCT01212757
Adverse Events Module:
NCT01212757