173 reports of this reaction
1.5% of all FLUOCINONIDE reports
#13 most reported adverse reaction
DERMATITIS ATOPIC is the #13 most commonly reported adverse reaction for FLUOCINONIDE, manufactured by Bausch Health US, LLC. There are 173 FDA adverse event reports linking FLUOCINONIDE to DERMATITIS ATOPIC. This represents approximately 1.5% of all 11,702 adverse event reports for this drug.
Patients taking FLUOCINONIDE who experience dermatitis atopic should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DERMATITIS ATOPIC is a less commonly reported adverse event for FLUOCINONIDE, but still significant enough to appear in the safety profile.
In addition to dermatitis atopic, the following adverse reactions have been reported for FLUOCINONIDE:
The following drugs have also been linked to dermatitis atopic in FDA adverse event reports:
DERMATITIS ATOPIC has been reported as an adverse event in 173 FDA reports for FLUOCINONIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DERMATITIS ATOPIC accounts for approximately 1.5% of all adverse event reports for FLUOCINONIDE, making it a notable side effect.
If you experience dermatitis atopic 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.