12,907 reports of this reaction
1.7% of all RITUXIMAB reports
#6 most reported adverse reaction
RASH is the #6 most commonly reported adverse reaction for RITUXIMAB, manufactured by Genentech, Inc.. There are 12,907 FDA adverse event reports linking RITUXIMAB to RASH. This represents approximately 1.7% of all 743,156 adverse event reports for this drug.
RITUXIMAB has an overall safety score of 85 out of 100. Patients taking RITUXIMAB 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 a less commonly reported adverse event for RITUXIMAB, but still significant enough to appear in the safety profile.
In addition to rash, the following adverse reactions have been reported for RITUXIMAB:
The following drugs have also been linked to rash in FDA adverse event reports:
RASH has been reported as an adverse event in 12,907 FDA reports for RITUXIMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
RASH accounts for approximately 1.7% of all adverse event reports for RITUXIMAB, making it a notable side effect.
If you experience rash while taking RITUXIMAB, 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.