88 reports of this reaction
5.1% of all PYRITHIONE ZINC reports
#1 most reported adverse reaction
PRURITUS is the #1 most commonly reported adverse reaction for PYRITHIONE ZINC, manufactured by Wal-Mart Stores Inc. There are 88 FDA adverse event reports linking PYRITHIONE ZINC to PRURITUS. This represents approximately 5.1% of all 1,712 adverse event reports for this drug.
Patients taking PYRITHIONE ZINC 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 PYRITHIONE ZINC users, representing a notable but not dominant share of adverse events.
In addition to pruritus, the following adverse reactions have been reported for PYRITHIONE ZINC:
The following drugs have also been linked to pruritus in FDA adverse event reports:
PRURITUS has been reported as an adverse event in 88 FDA reports for PYRITHIONE ZINC. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRURITUS accounts for approximately 5.1% of all adverse event reports for PYRITHIONE ZINC, making it one of the most commonly reported side effect.
If you experience pruritus while taking PYRITHIONE ZINC, 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.