6,122 reports of this reaction
10.9% of all ABIRATERONE ACETATE reports
#1 most reported adverse reaction
DEATH is the #1 most commonly reported adverse reaction for ABIRATERONE ACETATE, manufactured by Janssen Biotech, Inc.. There are 6,122 FDA adverse event reports linking ABIRATERONE ACETATE to DEATH. This represents approximately 10.9% of all 56,299 adverse event reports for this drug.
Patients taking ABIRATERONE ACETATE who experience death should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEATH is a frequently reported adverse event for ABIRATERONE ACETATE, accounting for a significant proportion of all reports.
In addition to death, the following adverse reactions have been reported for ABIRATERONE ACETATE:
The following drugs have also been linked to death in FDA adverse event reports:
DEATH has been reported as an adverse event in 6,122 FDA reports for ABIRATERONE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEATH accounts for approximately 10.9% of all adverse event reports for ABIRATERONE ACETATE, making it one of the most commonly reported side effect.
If you experience death while taking ABIRATERONE ACETATE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.