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: 2025-12-25 @ 4:05 AM
Ignite Modification Date: 2025-12-26 @ 3:01 AM
NCT ID: NCT00943202
Term: Irritability
Organ System: General disorders
Assessment Type: SYSTEMATIC_ASSESSMENT
Source Vocabulary: MedDRA (13.0)
Notes: Solicited from participants aged 6 to less than 36 months only.
Study: NCT00943202
Study Brief: Sanofi Pasteur, TIV + H1N1, Pediatric Population
Other Event Stats (If Any):

Other Event Stats

Group ID # Events # Affected # At Risk View
EG000 38 22 35 View
EG001 45 20 33 View
EG002 42 23 35 View
EG003 28 17 28 View