256 reports of this reaction
1.6% of all CHLORPHENIRAMINE MALEATE reports
#12 most reported adverse reaction
NEUROPATHY PERIPHERAL is the #12 most commonly reported adverse reaction for CHLORPHENIRAMINE MALEATE, manufactured by Rite Aid Corporation. There are 256 FDA adverse event reports linking CHLORPHENIRAMINE MALEATE to NEUROPATHY PERIPHERAL. This represents approximately 1.6% of all 15,638 adverse event reports for this drug.
Patients taking CHLORPHENIRAMINE MALEATE 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 CHLORPHENIRAMINE MALEATE, but still significant enough to appear in the safety profile.
In addition to neuropathy peripheral, the following adverse reactions have been reported for CHLORPHENIRAMINE MALEATE:
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 256 FDA reports for CHLORPHENIRAMINE MALEATE. 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 CHLORPHENIRAMINE MALEATE, making it a notable side effect.
If you experience neuropathy peripheral while taking CHLORPHENIRAMINE MALEATE, 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.