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 @ 3:31 PM
Ignite Modification Date:
2025-12-25 @ 1:45 PM
NCT ID:
NCT03789292
Group ID:
EG001
Title:
Treatment 1: EU-approved Humira
Description:
Patients were administered EU-approved Humira (40mg/0.4mL) by SC injection via PFS EOW in combination with MTX and folic acid from Week 0 to Week 24.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
324
Other Number Affected:
118
Other Number At Risk:
324
Study:
NCT03789292
Results Section:
NCT03789292
Adverse Events Module:
NCT03789292