230 reports of this reaction
3.6% of all CEFADROXIL reports
#3 most reported adverse reaction
DRUG HYPERSENSITIVITY is the #3 most commonly reported adverse reaction for CEFADROXIL, manufactured by Aurobindo Pharma Limited. There are 230 FDA adverse event reports linking CEFADROXIL to DRUG HYPERSENSITIVITY. This represents approximately 3.6% of all 6,348 adverse event reports for this drug.
Patients taking CEFADROXIL who experience drug 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.
DRUG HYPERSENSITIVITY is moderately reported among CEFADROXIL users, representing a notable but not dominant share of adverse events.
In addition to drug hypersensitivity, the following adverse reactions have been reported for CEFADROXIL:
The following drugs have also been linked to drug hypersensitivity in FDA adverse event reports:
DRUG HYPERSENSITIVITY has been reported as an adverse event in 230 FDA reports for CEFADROXIL. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRUG HYPERSENSITIVITY accounts for approximately 3.6% of all adverse event reports for CEFADROXIL, making it one of the most commonly reported side effect.
If you experience drug hypersensitivity while taking CEFADROXIL, 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.