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 @ 4:23 AM
Ignite Modification Date:
2025-12-26 @ 3:25 AM
NCT ID:
NCT02022020
Group ID:
EG000
Title:
Dabigatran (Pradax® in Canada; Pradaxa® in the United States
Description:
Patients with Non-Valvular Atrial Fibrillation (NVAF) at two countries (United States and Canada) who received dabigatran etexilate (dabigatran capsules were approved at the 75 mg, 110 mg and 150 mg dosages, and the recommended dosing is orally twice daily).
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
184
Serious Number At Risk:
220
Other Number Affected:
79
Other Number At Risk:
220
Study:
NCT02022020
Results Section:
NCT02022020
Adverse Events Module:
NCT02022020