3 reports of this reaction
12.5% of all TITANIUM DIOXIDE, ZINC OXIDE reports
#1 most reported adverse reaction
SUNBURN is the #1 most commonly reported adverse reaction for TITANIUM DIOXIDE, ZINC OXIDE, manufactured by Edgewell Personal Care Brands LLC. There are 3 FDA adverse event reports linking TITANIUM DIOXIDE, ZINC OXIDE to SUNBURN. This represents approximately 12.5% of all 24 adverse event reports for this drug.
Patients taking TITANIUM DIOXIDE, ZINC OXIDE who experience sunburn should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SUNBURN is a frequently reported adverse event for TITANIUM DIOXIDE, ZINC OXIDE, accounting for a significant proportion of all reports.
In addition to sunburn, the following adverse reactions have been reported for TITANIUM DIOXIDE, ZINC OXIDE:
The following drugs have also been linked to sunburn in FDA adverse event reports:
SUNBURN has been reported as an adverse event in 3 FDA reports for TITANIUM DIOXIDE, ZINC OXIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
SUNBURN accounts for approximately 12.5% of all adverse event reports for TITANIUM DIOXIDE, ZINC OXIDE, making it one of the most commonly reported side effect.
If you experience sunburn while taking TITANIUM DIOXIDE, 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.