Other Event

Other Event

Other Adverse Events are non-serious adverse events that exceed a specific frequency threshold (typically 5% within any study arm). These events are reported to provide comprehensive safety information about all noteworthy adverse occurrences during clinical trials. Each other event is categorized by term, organ system, assessment type, and source vocabulary for standardized reporting.

Other Event path is as follows:

Study -> Results Section -> Adverse Events Module -> Other Event

Study -> Results Section -> Adverse Events Module -> Other Event -> Other Event Stats

Other Event


Ignite Creation Date: 2025-12-24 @ 12:42 PM
Ignite Modification Date: 2025-12-25 @ 12:13 PM
NCT ID: NCT01570361
Term: Hyperlipidaemia
Organ System: Metabolism and nutrition disorders
Assessment Type: SYSTEMATIC_ASSESSMENT
Source Vocabulary: MedDRA v19.0
Notes: None
Study: NCT01570361
Study Brief: Atrial Fibrillation Progression Trial
Other Event Stats (If Any):

Other Event Stats

Group ID # Events # Affected # At Risk View
EG002 0 0 15 View
EG003 0 0 15 View
EG000 0 0 102 View
EG001 1 1 108 View