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 @ 11:47 AM
Ignite Modification Date:
2025-12-26 @ 10:19 AM
NCT ID:
NCT01432561
Group ID:
EG000
Title:
Cysteamine Bitartrate
Description:
Cysteamine bitartrate, 500mg once a day, three days.
Cysteamine bitartrate : 500 mg total, single dose taken orally on visits 2, 3 \& 4 which must occur within a 14 day period.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
8
Other Number Affected:
3
Other Number At Risk:
8
Study:
NCT01432561
Results Section:
NCT01432561
Adverse Events Module:
NCT01432561