1 reports of this reaction
16.7% of all OCTINOXATE, TITANIUM DIOXIDE reports
#6 most reported adverse reaction
SKIN IRRITATION is the #6 most commonly reported adverse reaction for OCTINOXATE, TITANIUM DIOXIDE, manufactured by NARS Cosmetics. There are 1 FDA adverse event reports linking OCTINOXATE, TITANIUM DIOXIDE to SKIN IRRITATION. This represents approximately 16.7% of all 6 adverse event reports for this drug.
Patients taking OCTINOXATE, TITANIUM DIOXIDE who experience skin irritation should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SKIN IRRITATION is a frequently reported adverse event for OCTINOXATE, TITANIUM DIOXIDE, accounting for a significant proportion of all reports.
In addition to skin irritation, the following adverse reactions have been reported for OCTINOXATE, TITANIUM DIOXIDE:
The following drugs have also been linked to skin irritation in FDA adverse event reports:
SKIN IRRITATION has been reported as an adverse event in 1 FDA reports for OCTINOXATE, TITANIUM DIOXIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
SKIN IRRITATION accounts for approximately 16.7% of all adverse event reports for OCTINOXATE, TITANIUM DIOXIDE, making it a notable side effect.
If you experience skin irritation while taking OCTINOXATE, TITANIUM DIOXIDE, 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.