61 reports of this reaction
2.0% of all HALOBETASOL PROPIONATE reports
#8 most reported adverse reaction
ARTHRALGIA is the #8 most commonly reported adverse reaction for HALOBETASOL PROPIONATE, manufactured by Lacer Pharma, LLC. There are 61 FDA adverse event reports linking HALOBETASOL PROPIONATE to ARTHRALGIA. This represents approximately 2.0% of all 3,036 adverse event reports for this drug.
Patients taking HALOBETASOL PROPIONATE 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 HALOBETASOL PROPIONATE, but still significant enough to appear in the safety profile.
In addition to arthralgia, the following adverse reactions have been reported for HALOBETASOL PROPIONATE:
The following drugs have also been linked to arthralgia in FDA adverse event reports:
ARTHRALGIA has been reported as an adverse event in 61 FDA reports for HALOBETASOL PROPIONATE. 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 HALOBETASOL PROPIONATE, making it a notable side effect.
If you experience arthralgia while taking HALOBETASOL PROPIONATE, 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.