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 @ 3:45 AM
Ignite Modification Date:
2025-12-26 @ 2:32 AM
NCT ID:
NCT03336502
Group ID:
EG000
Title:
POS IV (MK-5592)
Description:
POS 300 mg intravenous (IV) infusion twice on Day 1 followed by 300 mg IV infusion once daily on Days 2 to 10 (±1). At the discretion of the investigator, participants may have received POS 300 mg IV infusion once daily or 200 mg oral suspension 3 times daily for up to 18 additional days
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
15
Serious Number At Risk:
70
Other Number Affected:
70
Other Number At Risk:
70
Study:
NCT03336502
Results Section:
NCT03336502
Adverse Events Module:
NCT03336502