1 reports of this reaction
1.4% of all TITANIUM DIOXIDE AND ZINC OXIDE reports
#16 most reported adverse reaction
APPLICATION SITE BURN is the #16 most commonly reported adverse reaction for TITANIUM DIOXIDE AND ZINC OXIDE, manufactured by KAS Direct LLC dba BabyGanics. There are 1 FDA adverse event reports linking TITANIUM DIOXIDE AND ZINC OXIDE to APPLICATION SITE BURN. This represents approximately 1.4% of all 69 adverse event reports for this drug.
Patients taking TITANIUM DIOXIDE AND ZINC OXIDE who experience application site burn should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
APPLICATION SITE BURN is a less commonly reported adverse event for TITANIUM DIOXIDE AND ZINC OXIDE, but still significant enough to appear in the safety profile.
In addition to application site burn, the following adverse reactions have been reported for TITANIUM DIOXIDE AND ZINC OXIDE:
The following drugs have also been linked to application site burn in FDA adverse event reports:
APPLICATION SITE BURN has been reported as an adverse event in 1 FDA reports for TITANIUM DIOXIDE AND ZINC OXIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
APPLICATION SITE BURN accounts for approximately 1.4% of all adverse event reports for TITANIUM DIOXIDE AND ZINC OXIDE, making it a notable side effect.
If you experience application site burn while taking TITANIUM DIOXIDE AND 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.