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 @ 11:44 PM
Ignite Modification Date:
2025-12-25 @ 9:37 PM
NCT ID:
NCT01969851
Group ID:
EG000
Title:
Lacosamide 1 Month - <4 Years
Description:
Subjects, aged 1 month to \<4 years, who were administered Lacosamide oral solution (for subjects weighing \<50 kg) or tablet (for subjects weighing \>=50 kg). The initial dose of 2 mg/kg/day (for subjects weighing \<50 kg), or 100 mg/day (for subjects weighing \>=50 kg) was titrated to optimize tolerability and seizure control to at least 4 mg/kg/day for subjects weighing \<50 kg, or 200 mg/day for subjects weighing \>=50 kg; not to exceed 12 mg/kg/day for subjects weighing \<50 kg, or 600 mg/day in subjects weighing \>=50 kg.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
10
Other Number Affected:
10
Other Number At Risk:
10
Study:
NCT01969851
Results Section:
NCT01969851
Adverse Events Module:
NCT01969851