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 @ 9:16 PM
Ignite Modification Date:
2025-12-25 @ 7:04 PM
NCT ID:
NCT02747004
Group ID:
EG002
Title:
200mg Abemaciclib + 2mg Prophylactic Loperamide
Description:
Participants received oral dose of 200 milligrams (mg) Abemaciclib every 12 hours (Q12H) along with 2mg Prophylactic Loperamide on days 1 to days 28 of a 28 day cycle.
Note: During Cycle 1, 2mg prophylactic loperamide was administered orally with the first dose of abemaciclib daily. During Cycle 2 and beyond, loperamide was administered at investigator's discretion and/or if clinically indicated.
Deaths Number Affected:
29
Deaths Number At Risk:
None
Serious Number Affected:
21
Serious Number At Risk:
77
Other Number Affected:
75
Other Number At Risk:
77
Study:
NCT02747004
Results Section:
NCT02747004
Adverse Events Module:
NCT02747004