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 @ 4:05 AM
Ignite Modification Date:
2025-12-26 @ 3:01 AM
NCT ID:
NCT01552902
Group ID:
EG002
Title:
Methylphenidate
Description:
Methylphenidate (Concerta, OROS-MPH) 18 to 72 mg over encapsulated capsule once daily orally along with placebo over encapsulated capsule (no placebo administered when methylphenidate 72 mg \[2\*36 mg capsules\] was administered) for 4 weeks (forced dose titration), followed by methylphenidate 72 mg (2\*36 mg capsules) over encapsulated capsule once daily orally for 2 weeks (dose maintenance).
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
219
Other Number Affected:
99
Other Number At Risk:
219
Study:
NCT01552902
Results Section:
NCT01552902
Adverse Events Module:
NCT01552902