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:
2025-12-26 @ 10:44 PM
Ignite Modification Date:
2025-12-26 @ 10:44 PM
NCT ID:
NCT02435212
Group ID:
EG002
Title:
DFX Granules - Core Phase
Description:
Participants received deferasirox (DFX) granules orally once daily based on body weight in the form of stick packs for 48 weeks in the Core phase. The starting dose was 14 mg/kg/day which was then adjusted based on tolerability, safety and efficacy considerations.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
27
Serious Number At Risk:
110
Other Number Affected:
97
Other Number At Risk:
110
Study:
NCT02435212
Results Section:
NCT02435212
Adverse Events Module:
NCT02435212