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 @ 2:10 AM
Ignite Modification Date:
2025-12-26 @ 12:37 AM
NCT ID:
NCT01466660
Group ID:
EG001
Title:
Gefitinib
Description:
Gefitinib film-coated tablets, administered orally, once daily. Starting dose was 250mg, the investigator was allowed to modify dosing in the presence of drug-related adverse events. Continuous daily dosing until disease progression, occurrence of unacceptable adverse events, or other reason necessitating withdrawal.
Deaths Number Affected:
132
Deaths Number At Risk:
None
Serious Number Affected:
64
Serious Number At Risk:
159
Other Number Affected:
159
Other Number At Risk:
159
Study:
NCT01466660
Results Section:
NCT01466660
Adverse Events Module:
NCT01466660