9 reports of this reaction
2.4% of all AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE reports
#5 most reported adverse reaction
SUNBURN is the #5 most commonly reported adverse reaction for AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE, manufactured by The Kroger Co.. There are 9 FDA adverse event reports linking AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE to SUNBURN. This represents approximately 2.4% of all 376 adverse event reports for this drug.
Patients taking AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE 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 less commonly reported adverse event for AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE, but still significant enough to appear in the safety profile.
In addition to sunburn, the following adverse reactions have been reported for AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE:
The following drugs have also been linked to sunburn in FDA adverse event reports:
SUNBURN has been reported as an adverse event in 9 FDA reports for AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
SUNBURN accounts for approximately 2.4% of all adverse event reports for AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE, making it a notable side effect.
If you experience sunburn while taking AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE, 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.