82 reports of this reaction
3.9% of all TAZAROTENE reports
#2 most reported adverse reaction
ERYTHEMA is the #2 most commonly reported adverse reaction for TAZAROTENE, manufactured by Almirall, LLC. There are 82 FDA adverse event reports linking TAZAROTENE to ERYTHEMA. This represents approximately 3.9% of all 2,077 adverse event reports for this drug.
Patients taking TAZAROTENE who experience erythema should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ERYTHEMA is moderately reported among TAZAROTENE users, representing a notable but not dominant share of adverse events.
In addition to erythema, the following adverse reactions have been reported for TAZAROTENE:
The following drugs have also been linked to erythema in FDA adverse event reports:
ERYTHEMA has been reported as an adverse event in 82 FDA reports for TAZAROTENE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ERYTHEMA accounts for approximately 3.9% of all adverse event reports for TAZAROTENE, making it one of the most commonly reported side effect.
If you experience erythema while taking TAZAROTENE, 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.