2,549 reports of this reaction
12.2% of all SULFUR reports
#1 most reported adverse reaction
DRY SKIN is the #1 most commonly reported adverse reaction for SULFUR, manufactured by Alchemee, LLC. There are 2,549 FDA adverse event reports linking SULFUR to DRY SKIN. This represents approximately 12.2% of all 20,945 adverse event reports for this drug.
Patients taking SULFUR 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 SULFUR, accounting for a significant proportion of all reports.
In addition to dry skin, the following adverse reactions have been reported for SULFUR:
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 2,549 FDA reports for SULFUR. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRY SKIN accounts for approximately 12.2% of all adverse event reports for SULFUR, making it one of the most commonly reported side effect.
If you experience dry skin while taking SULFUR, 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.