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 @ 1:22 AM
Ignite Modification Date: 2025-12-25 @ 11:31 PM
NCT ID: NCT00997893
Term: Non-serious; irregular uterine bleeding
Organ System: Reproductive system and breast disorders
Assessment Type: NON_SYSTEMATIC_ASSESSMENT
Source Vocabulary: None
Notes: Participant had heavy and moderate uterine bleeding. Exam and transvaginal ultrasound was performed. Possible hyperplasia was found and later biopsied with benign results. Event was self reported by participant.
Study: NCT00997893
Study Brief: Research Investigation of Soy and Estrogen
Other Event Stats (If Any):

Other Event Stats

Group ID # Events # Affected # At Risk View
EG000 1 1 14 View
EG001 0 0 13 View
EG002 0 0 13 View