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 @ 2:12 PM
Ignite Modification Date:
2025-12-25 @ 12:51 PM
NCT ID:
NCT01124695
Group ID:
EG000
Title:
Tamoxifen
Description:
Patients receive oral tamoxifen citrate at 20 mg once daily on days 1-28. Treatment repeats every 28 days in the absence of disease progression or unacceptable toxicities.
Deaths Number Affected:
69
Deaths Number At Risk:
None
Serious Number Affected:
30
Serious Number At Risk:
122
Other Number Affected:
18
Other Number At Risk:
122
Study:
NCT01124695
Results Section:
NCT01124695
Adverse Events Module:
NCT01124695