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 @ 7:15 PM
Ignite Modification Date:
2025-12-25 @ 4:53 PM
NCT ID:
NCT01095003
Group ID:
EG001
Title:
Capecitabine Single-agent
Description:
Capecitabine: Capecitabine 825mg/m² per os twice per day for 14 consecutive days starting day 1 of each cycle repeated every 3 weeks
Deaths Number Affected:
348
Deaths Number At Risk:
None
Serious Number Affected:
85
Serious Number At Risk:
383
Other Number Affected:
262
Other Number At Risk:
383
Study:
NCT01095003
Results Section:
NCT01095003
Adverse Events Module:
NCT01095003