406 reports of this reaction
3.5% of all FLUOCINONIDE reports
#4 most reported adverse reaction
PRURITUS is the #4 most commonly reported adverse reaction for FLUOCINONIDE, manufactured by Bausch Health US, LLC. There are 406 FDA adverse event reports linking FLUOCINONIDE to PRURITUS. This represents approximately 3.5% of all 11,702 adverse event reports for this drug.
Patients taking FLUOCINONIDE who experience pruritus should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRURITUS is moderately reported among FLUOCINONIDE users, representing a notable but not dominant share of adverse events.
In addition to pruritus, the following adverse reactions have been reported for FLUOCINONIDE:
The following drugs have also been linked to pruritus in FDA adverse event reports:
PRURITUS has been reported as an adverse event in 406 FDA reports for FLUOCINONIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRURITUS accounts for approximately 3.5% of all adverse event reports for FLUOCINONIDE, making it a notable side effect.
If you experience pruritus while taking FLUOCINONIDE, 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.