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 @ 5:12 AM
Ignite Modification Date:
2025-12-26 @ 4:17 AM
NCT ID:
NCT00266227
Group ID:
EG000
Title:
Arm A: Rituximab Retreatment
Description:
1000 mg rituximab intravenous initial treatment on day 1 and day 15 plus 10-25 mg/week methotrexate followed by re-treatment during weeks 24 -40 consisting of two additional doses of 1000 mg rituximab 14 days apart plus 10-25 mg/week methotrexate.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
42
Serious Number At Risk:
320
Other Number Affected:
291
Other Number At Risk:
320
Study:
NCT00266227
Results Section:
NCT00266227
Adverse Events Module:
NCT00266227