2,756 reports of this reaction
1.3% of all BEVACIZUMAB reports
#19 most reported adverse reaction
NEUROPATHY PERIPHERAL is the #19 most commonly reported adverse reaction for BEVACIZUMAB, manufactured by Genentech, Inc.. There are 2,756 FDA adverse event reports linking BEVACIZUMAB to NEUROPATHY PERIPHERAL. This represents approximately 1.3% of all 204,762 adverse event reports for this drug.
Patients taking BEVACIZUMAB who experience neuropathy peripheral should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NEUROPATHY PERIPHERAL is a less commonly reported adverse event for BEVACIZUMAB, but still significant enough to appear in the safety profile.
In addition to neuropathy peripheral, the following adverse reactions have been reported for BEVACIZUMAB:
The following drugs have also been linked to neuropathy peripheral in FDA adverse event reports:
NEUROPATHY PERIPHERAL has been reported as an adverse event in 2,756 FDA reports for BEVACIZUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
NEUROPATHY PERIPHERAL accounts for approximately 1.3% of all adverse event reports for BEVACIZUMAB, making it a notable side effect.
If you experience neuropathy peripheral while taking BEVACIZUMAB, 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.