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 @ 4:02 AM
Ignite Modification Date:
2025-12-26 @ 2:55 AM
NCT ID:
NCT01286402
Group ID:
EG000
Title:
Bupropion SR (Sustained Release)
Description:
Group receiving bupropion SR medication
Bupropion SR: - 150mg (1 pill), taken orally, taken daily for the 1st 3 days
\- 300mg (2 pills), taken orally, taken daily for the rest of the 8 weeks of drug treatment
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
5
Other Number Affected:
2
Other Number At Risk:
5
Study:
NCT01286402
Results Section:
NCT01286402
Adverse Events Module:
NCT01286402