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 @ 2:00 AM
Ignite Modification Date:
2025-12-26 @ 12:24 AM
NCT ID:
NCT02106494
Group ID:
EG001
Title:
Ondansetron + Fosaprepitant + Dexamethasone
Description:
Day 1 - Single IV dose of Ondansetron 0.15 mg/kg (up to a maximum of 16 mg) + Placebo for APF530 SC+ Fosaprepitant 150 mg IV + Dexamethasone 12 mg IV
Day 2 - Dexamethasone 8 mg PO QD
Days 3 and 4 - Dexamethasone 8 mg PO BID
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
28
Serious Number At Risk:
459
Other Number Affected:
407
Other Number At Risk:
459
Study:
NCT02106494
Results Section:
NCT02106494
Adverse Events Module:
NCT02106494