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 @ 2:31 AM
Ignite Modification Date:
2025-12-26 @ 1:06 AM
NCT ID:
NCT00355134
Group ID:
EG000
Title:
Core: Fingolimod 1.25 mg
Description:
Participants received 1.25 mg fingolimod orally once a day for up to 24 months during the core phase. Upon implementation of a protocol amendment, all patients taking 1.25 mg fingolimod were switched to 0.5 mg fingolimod orally once a day.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
53
Serious Number At Risk:
370
Other Number Affected:
335
Other Number At Risk:
370
Study:
NCT00355134
Results Section:
NCT00355134
Adverse Events Module:
NCT00355134