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:
2025-12-26 @ 1:18 PM
Ignite Modification Date:
2025-12-26 @ 1:18 PM
NCT ID:
NCT00331006
Group ID:
EG000
Title:
Rituximab
Description:
Rituximab administered at a dose of 375 mg/m\^2 by slow intravenous infusion once per week for 4 weeks
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
11
Serious Number At Risk:
16
Other Number Affected:
15
Other Number At Risk:
16
Study:
NCT00331006
Results Section:
NCT00331006
Adverse Events Module:
NCT00331006