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 @ 3:38 AM
Ignite Modification Date:
2025-12-26 @ 2:23 AM
NCT ID:
NCT00024102
Group ID:
EG002
Title:
Capecitabine
Description:
Capecitabine (2000 mg/m\^2 in 2 doses days 1-14) repeated every 21 days for 6 cycles
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
26
Serious Number At Risk:
299
Other Number Affected:
279
Other Number At Risk:
299
Study:
NCT00024102
Results Section:
NCT00024102
Adverse Events Module:
NCT00024102