1,277 reports of this reaction
2.3% of all ABIRATERONE ACETATE reports
#7 most reported adverse reaction
ASTHENIA is the #7 most commonly reported adverse reaction for ABIRATERONE ACETATE, manufactured by Janssen Biotech, Inc.. There are 1,277 FDA adverse event reports linking ABIRATERONE ACETATE to ASTHENIA. This represents approximately 2.3% of all 56,299 adverse event reports for this drug.
Patients taking ABIRATERONE ACETATE who experience asthenia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ASTHENIA is a less commonly reported adverse event for ABIRATERONE ACETATE, but still significant enough to appear in the safety profile.
In addition to asthenia, the following adverse reactions have been reported for ABIRATERONE ACETATE:
The following drugs have also been linked to asthenia in FDA adverse event reports:
ASTHENIA has been reported as an adverse event in 1,277 FDA reports for ABIRATERONE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ASTHENIA accounts for approximately 2.3% of all adverse event reports for ABIRATERONE ACETATE, making it a notable side effect.
If you experience asthenia 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.