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 @ 9:49 PM
Ignite Modification Date:
2025-12-25 @ 7:27 PM
NCT ID:
NCT00436332
Group ID:
EG000
Title:
Erlotinib and Bevacizumab
Description:
Patients receive oral erlotinib hydrochloride once daily on days 1-21 and bevacizumab IV over 30-90 minutes on day 1.
Deaths Number Affected:
56
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
79
Other Number Affected:
77
Other Number At Risk:
79
Study:
NCT00436332
Results Section:
NCT00436332
Adverse Events Module:
NCT00436332