2 reports of this reaction
1.9% of all SODIUM SULFACETAMIDE, SULFUR reports
#3 most reported adverse reaction
HYPERSENSITIVITY is the #3 most commonly reported adverse reaction for SODIUM SULFACETAMIDE, SULFUR, manufactured by Acella Pharmaceuticals, LLC. There are 2 FDA adverse event reports linking SODIUM SULFACETAMIDE, SULFUR to HYPERSENSITIVITY. This represents approximately 1.9% of all 106 adverse event reports for this drug.
Patients taking SODIUM SULFACETAMIDE, SULFUR 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 a less commonly reported adverse event for SODIUM SULFACETAMIDE, SULFUR, but still significant enough to appear in the safety profile.
In addition to hypersensitivity, the following adverse reactions have been reported for SODIUM SULFACETAMIDE, SULFUR:
The following drugs have also been linked to hypersensitivity in FDA adverse event reports:
HYPERSENSITIVITY has been reported as an adverse event in 2 FDA reports for SODIUM SULFACETAMIDE, SULFUR. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPERSENSITIVITY accounts for approximately 1.9% of all adverse event reports for SODIUM SULFACETAMIDE, SULFUR, making it one of the most commonly reported side effect.
If you experience hypersensitivity while taking SODIUM SULFACETAMIDE, 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.