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 @ 3:04 AM
Ignite Modification Date:
2025-12-26 @ 1:43 AM
NCT ID:
NCT02545933
Group ID:
EG001
Title:
Prasugrel/Ticagrelor Plus Vorapaxar
Description:
Prasugrel or ticagrelor plus vorapaxar 2.5mg od
Prasugrel: Patients will continue treatment with either prasugrel (10mg once daily) or ticagrelor (90mg twice/daily)
Vorapaxar: Vorapaxar will be administered at the dose of 2.5mg once daily
Ticagrelor: Patients will continue treatment with either prasugrel (10mg once daily) or ticagrelor (90mg twice/daily)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
43
Other Number Affected:
6
Other Number At Risk:
43
Study:
NCT02545933
Results Section:
NCT02545933
Adverse Events Module:
NCT02545933