2,235 reports of this reaction
4.3% of all CETUXIMAB reports
#1 most reported adverse reaction
RASH is the #1 most commonly reported adverse reaction for CETUXIMAB, manufactured by ImClone LLC. There are 2,235 FDA adverse event reports linking CETUXIMAB to RASH. This represents approximately 4.3% of all 51,547 adverse event reports for this drug.
Patients taking CETUXIMAB who experience rash should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
RASH is moderately reported among CETUXIMAB users, representing a notable but not dominant share of adverse events.
In addition to rash, the following adverse reactions have been reported for CETUXIMAB:
The following drugs have also been linked to rash in FDA adverse event reports:
RASH has been reported as an adverse event in 2,235 FDA reports for CETUXIMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
RASH accounts for approximately 4.3% of all adverse event reports for CETUXIMAB, making it one of the most commonly reported side effect.
If you experience rash while taking CETUXIMAB, 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.