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 @ 2:02 AM
Ignite Modification Date:
2025-12-26 @ 12:26 AM
NCT ID:
NCT02052960
Group ID:
EG001
Title:
Cetuximab
Description:
Cetuximab was administered once weekly as infusion to all patients randomized to the cetuximab arm.The initial dose was 400 mg/m2 body surface area (BSA) and each subsequent dose was 250 mg/m2 BSA.
Deaths Number Affected:
14
Deaths Number At Risk:
None
Serious Number Affected:
78
Serious Number At Risk:
122
Other Number Affected:
121
Other Number At Risk:
122
Study:
NCT02052960
Results Section:
NCT02052960
Adverse Events Module:
NCT02052960