DYSPNOEA is the #16 most commonly reported adverse reaction for ABIRATERONE ACETATE, manufactured by Janssen Biotech, Inc.. There are 779 FDA adverse event reports linking ABIRATERONE ACETATE to DYSPNOEA. This represents approximately 1.4% of all 56,299 adverse event reports for this drug.
Patients taking ABIRATERONE ACETATE who experience dyspnoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
Reporting Frequency
DYSPNOEA779 of 56,299 reports
DYSPNOEA is a less commonly reported adverse event for ABIRATERONE ACETATE, but still significant enough to appear in the safety profile.
Other Side Effects of ABIRATERONE ACETATE
In addition to dyspnoea, the following adverse reactions have been reported for ABIRATERONE ACETATE:
DYSPNOEA has been reported as an adverse event in 779 FDA reports for ABIRATERONE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is DYSPNOEA with ABIRATERONE ACETATE?
DYSPNOEA accounts for approximately 1.4% of all adverse event reports for ABIRATERONE ACETATE, making it a notable side effect.
What should I do if I experience DYSPNOEA while taking ABIRATERONE ACETATE?
If you experience dyspnoea 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.