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 @ 4:26 AM
Ignite Modification Date:
2025-12-26 @ 3:29 AM
NCT ID:
NCT02239120
Group ID:
EG000
Title:
Dabigatran Etexilate 110 or 150 Milligram (mg)
Description:
Participants were orally administered one 110 mg (for participants aged ≥75 years or with a creatinine clearance (CrCl) of 30 to \<50 millilitre/ minute (mL/min)) or one 150 mg (for participants aged \<75 years and with a CrCl of ≥50 mL/minute) Dabigatran etexilate (DE) capsule twice daily.
Deaths Number Affected:
56
Deaths Number At Risk:
None
Serious Number Affected:
724
Serious Number At Risk:
2676
Other Number Affected:
306
Other Number At Risk:
2676
Study:
NCT02239120
Results Section:
NCT02239120
Adverse Events Module:
NCT02239120