4 reports of this reaction
1.6% of all SULFACETAMIDE SODIUM, SULFUR reports
#10 most reported adverse reaction
DRY SKIN is the #10 most commonly reported adverse reaction for SULFACETAMIDE SODIUM, SULFUR, manufactured by Aurobindo Pharma Limited. There are 4 FDA adverse event reports linking SULFACETAMIDE SODIUM, SULFUR to DRY SKIN. This represents approximately 1.6% of all 251 adverse event reports for this drug.
Patients taking SULFACETAMIDE SODIUM, 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 less commonly reported adverse event for SULFACETAMIDE SODIUM, SULFUR, but still significant enough to appear in the safety profile.
In addition to dry skin, the following adverse reactions have been reported for SULFACETAMIDE SODIUM, 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 4 FDA reports for SULFACETAMIDE SODIUM, SULFUR. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRY SKIN accounts for approximately 1.6% of all adverse event reports for SULFACETAMIDE SODIUM, SULFUR, making it a notable side effect.
If you experience dry skin while taking SULFACETAMIDE SODIUM, 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.