1,429 reports of this reaction
4.2% of all REGORAFENIB reports
#3 most reported adverse reaction
PALMAR PLANTAR ERYTHRODYSAESTHESIA SYNDROME is the #3 most commonly reported adverse reaction for REGORAFENIB, manufactured by Bayer HealthCare Pharmaceuticals Inc.. There are 1,429 FDA adverse event reports linking REGORAFENIB to PALMAR PLANTAR ERYTHRODYSAESTHESIA SYNDROME. This represents approximately 4.2% of all 34,211 adverse event reports for this drug.
Patients taking REGORAFENIB who experience palmar plantar erythrodysaesthesia syndrome should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PALMAR PLANTAR ERYTHRODYSAESTHESIA SYNDROME is moderately reported among REGORAFENIB users, representing a notable but not dominant share of adverse events.
In addition to palmar plantar erythrodysaesthesia syndrome, the following adverse reactions have been reported for REGORAFENIB:
The following drugs have also been linked to palmar plantar erythrodysaesthesia syndrome in FDA adverse event reports:
PALMAR PLANTAR ERYTHRODYSAESTHESIA SYNDROME has been reported as an adverse event in 1,429 FDA reports for REGORAFENIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
PALMAR PLANTAR ERYTHRODYSAESTHESIA SYNDROME accounts for approximately 4.2% of all adverse event reports for REGORAFENIB, making it one of the most commonly reported side effect.
If you experience palmar plantar erythrodysaesthesia syndrome while taking REGORAFENIB, 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.