2,768 reports of this reaction
1.6% of all CAPECITABINE reports
#13 most reported adverse reaction
NEUROPATHY PERIPHERAL is the #13 most commonly reported adverse reaction for CAPECITABINE, manufactured by H2-Pharma, LLC. There are 2,768 FDA adverse event reports linking CAPECITABINE to NEUROPATHY PERIPHERAL. This represents approximately 1.6% of all 174,965 adverse event reports for this drug.
Patients taking CAPECITABINE 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 CAPECITABINE, but still significant enough to appear in the safety profile.
In addition to neuropathy peripheral, the following adverse reactions have been reported for CAPECITABINE:
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 2,768 FDA reports for CAPECITABINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NEUROPATHY PERIPHERAL accounts for approximately 1.6% of all adverse event reports for CAPECITABINE, making it a notable side effect.
If you experience neuropathy peripheral while taking CAPECITABINE, 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.