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 @ 4:03 AM
Ignite Modification Date:
2025-12-26 @ 2:58 AM
NCT ID:
NCT02704702
Group ID:
EG004
Title:
Treatment C(Single Dose)
Description:
Sequence 1(ABC)/Sequence 2(ACB)/Sequence 3(BAC)/Sequence 4(BCA)/Sequence 5(CAB)/Sequence 6(CBA)
There will be a washout of at least 7 days between the each period.
Treatment A: Fimasartan
Treatment B: Rosuvastatin
Treatment C: Fimasartan + Rosuvastatin
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
34
Other Number Affected:
6
Other Number At Risk:
34
Study:
NCT02704702
Results Section:
NCT02704702
Adverse Events Module:
NCT02704702