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 @ 5:12 PM
Ignite Modification Date:
2025-12-25 @ 2:50 PM
NCT ID:
NCT01468350
Group ID:
EG001
Title:
PART A: Dalfampridine-ER 10mg
Description:
6 subjects randomized into Sequence BA (placebo - dalfampridine-ER) 5 subjects randomized into Sequence AB (dalfampridine-ER - placebo)
A single witnessed dose of placebo and a single witnessed dose of dalfampridine-ER 10 mg, two days apart
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
11
Other Number Affected:
2
Other Number At Risk:
11
Study:
NCT01468350
Results Section:
NCT01468350
Adverse Events Module:
NCT01468350