298 reports of this reaction
3.2% of all ZINC OXIDE reports
#4 most reported adverse reaction
OFF LABEL USE is the #4 most commonly reported adverse reaction for ZINC OXIDE, manufactured by MONAT GLOBAL CORP. There are 298 FDA adverse event reports linking ZINC OXIDE to OFF LABEL USE. This represents approximately 3.2% of all 9,433 adverse event reports for this drug.
Patients taking ZINC OXIDE who experience off label use should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OFF LABEL USE is moderately reported among ZINC OXIDE users, representing a notable but not dominant share of adverse events.
In addition to off label use, the following adverse reactions have been reported for ZINC OXIDE:
The following drugs have also been linked to off label use in FDA adverse event reports:
OFF LABEL USE has been reported as an adverse event in 298 FDA reports for ZINC OXIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 3.2% of all adverse event reports for ZINC OXIDE, making it a notable side effect.
If you experience off label use while taking ZINC OXIDE, 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.