447 reports of this reaction
2.8% of all CRISABOROLE reports
#9 most reported adverse reaction
ECZEMA is the #9 most commonly reported adverse reaction for CRISABOROLE, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 447 FDA adverse event reports linking CRISABOROLE to ECZEMA. This represents approximately 2.8% of all 15,699 adverse event reports for this drug.
Patients taking CRISABOROLE who experience eczema should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ECZEMA is a less commonly reported adverse event for CRISABOROLE, but still significant enough to appear in the safety profile.
In addition to eczema, the following adverse reactions have been reported for CRISABOROLE:
The following drugs have also been linked to eczema in FDA adverse event reports:
ECZEMA has been reported as an adverse event in 447 FDA reports for CRISABOROLE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ECZEMA accounts for approximately 2.8% of all adverse event reports for CRISABOROLE, making it a notable side effect.
If you experience eczema while taking CRISABOROLE, 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.