6 reports of this reaction
5.6% of all OCTINOXATE reports
#6 most reported adverse reaction
HYPERSENSITIVITY is the #6 most commonly reported adverse reaction for OCTINOXATE, manufactured by ALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETI. There are 6 FDA adverse event reports linking OCTINOXATE to HYPERSENSITIVITY. This represents approximately 5.6% of all 107 adverse event reports for this drug.
Patients taking OCTINOXATE who experience hypersensitivity should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPERSENSITIVITY is moderately reported among OCTINOXATE users, representing a notable but not dominant share of adverse events.
In addition to hypersensitivity, the following adverse reactions have been reported for OCTINOXATE:
The following drugs have also been linked to hypersensitivity in FDA adverse event reports:
HYPERSENSITIVITY has been reported as an adverse event in 6 FDA reports for OCTINOXATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPERSENSITIVITY accounts for approximately 5.6% of all adverse event reports for OCTINOXATE, making it a notable side effect.
If you experience hypersensitivity while taking OCTINOXATE, 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.