31 reports of this reaction
1.8% of all PYRITHIONE ZINC reports
#10 most reported adverse reaction
PRODUCT USE ISSUE is the #10 most commonly reported adverse reaction for PYRITHIONE ZINC, manufactured by Wal-Mart Stores Inc. There are 31 FDA adverse event reports linking PYRITHIONE ZINC to PRODUCT USE ISSUE. This represents approximately 1.8% of all 1,712 adverse event reports for this drug.
Patients taking PYRITHIONE ZINC who experience product use issue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRODUCT USE ISSUE is a less commonly reported adverse event for PYRITHIONE ZINC, but still significant enough to appear in the safety profile.
In addition to product use issue, the following adverse reactions have been reported for PYRITHIONE ZINC:
The following drugs have also been linked to product use issue in FDA adverse event reports:
PRODUCT USE ISSUE has been reported as an adverse event in 31 FDA reports for PYRITHIONE ZINC. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT USE ISSUE accounts for approximately 1.8% of all adverse event reports for PYRITHIONE ZINC, making it a notable side effect.
If you experience product use issue 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.