329 reports of this reaction
2.0% of all APALUTAMIDE reports
#10 most reported adverse reaction
ARTHRALGIA is the #10 most commonly reported adverse reaction for APALUTAMIDE, manufactured by Janssen Products, LP. There are 329 FDA adverse event reports linking APALUTAMIDE to ARTHRALGIA. This represents approximately 2.0% of all 16,304 adverse event reports for this drug.
Patients taking APALUTAMIDE who experience arthralgia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ARTHRALGIA is a less commonly reported adverse event for APALUTAMIDE, but still significant enough to appear in the safety profile.
In addition to arthralgia, the following adverse reactions have been reported for APALUTAMIDE:
The following drugs have also been linked to arthralgia in FDA adverse event reports:
ARTHRALGIA has been reported as an adverse event in 329 FDA reports for APALUTAMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ARTHRALGIA accounts for approximately 2.0% of all adverse event reports for APALUTAMIDE, making it a notable side effect.
If you experience arthralgia while taking APALUTAMIDE, 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.