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:
2025-12-24 @ 4:13 PM
Ignite Modification Date:
2025-12-25 @ 2:12 PM
NCT ID:
NCT00110266
Group ID:
EG000
Title:
Deferasirox
Description:
Participants received Deferasirox 20 mg/kg/day orally OD for one year. The appropriate daily dose was calculated by participants actual body weight. Deferasirox was taken every morning 30 minutes before breakfast, preferably around the same time between 7:00 and 9:00 AM each day. The tablets was dropped into water or apple juice or orange juice and gently stirred for 1 to 3 minutes until completely dispersed.
Deaths Number Affected:
17
Deaths Number At Risk:
None
Serious Number Affected:
78
Serious Number At Risk:
173
Other Number Affected:
166
Other Number At Risk:
173
Study:
NCT00110266
Results Section:
NCT00110266
Adverse Events Module:
NCT00110266