12,764 reports of this reaction
10.1% of all SALICYLIC ACID reports
#2 most reported adverse reaction
DRY SKIN is the #2 most commonly reported adverse reaction for SALICYLIC ACID, manufactured by Alchemee, LLC. There are 12,764 FDA adverse event reports linking SALICYLIC ACID to DRY SKIN. This represents approximately 10.1% of all 126,851 adverse event reports for this drug.
SALICYLIC ACID has an overall safety score of 65 out of 100. Patients taking SALICYLIC ACID who experience dry skin should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRY SKIN is a frequently reported adverse event for SALICYLIC ACID, accounting for a significant proportion of all reports.
In addition to dry skin, the following adverse reactions have been reported for SALICYLIC ACID:
The following drugs have also been linked to dry skin in FDA adverse event reports:
DRY SKIN has been reported as an adverse event in 12,764 FDA reports for SALICYLIC ACID. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRY SKIN accounts for approximately 10.1% of all adverse event reports for SALICYLIC ACID, making it one of the most commonly reported side effect.
If you experience dry skin while taking SALICYLIC ACID, 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.