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 @ 4:34 AM
Ignite Modification Date:
2025-12-26 @ 3:35 AM
NCT ID:
NCT00413218
Group ID:
EG000
Title:
Isavuconazole (ISA)
Description:
Participants received 3 intravenous (IV) loading doses of 200 mg of isavuconazole on days 1 and 2, followed by an IV maintenance dose of 200 mg once daily from day 3 to day 56. On day 11 at the discretion of the investigator, non-neutropenic patients could switch from IV to oral therapy. Oral therapy consisted of 200 mg isavuconazole once daily.
Deaths Number Affected:
55
Deaths Number At Risk:
None
Serious Number Affected:
112
Serious Number At Risk:
220
Other Number Affected:
162
Other Number At Risk:
220
Study:
NCT00413218
Results Section:
NCT00413218
Adverse Events Module:
NCT00413218