10 reports of this reaction
1.5% of all BENZOCAINE AND MENTHOL reports
#15 most reported adverse reaction
CHRONIC KIDNEY DISEASE is the #15 most commonly reported adverse reaction for BENZOCAINE AND MENTHOL, manufactured by RB Health (US) LLC. There are 10 FDA adverse event reports linking BENZOCAINE AND MENTHOL to CHRONIC KIDNEY DISEASE. This represents approximately 1.5% of all 672 adverse event reports for this drug.
Patients taking BENZOCAINE AND MENTHOL who experience chronic kidney disease should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
CHRONIC KIDNEY DISEASE is a less commonly reported adverse event for BENZOCAINE AND MENTHOL, but still significant enough to appear in the safety profile.
In addition to chronic kidney disease, the following adverse reactions have been reported for BENZOCAINE AND MENTHOL:
The following drugs have also been linked to chronic kidney disease in FDA adverse event reports:
CHRONIC KIDNEY DISEASE has been reported as an adverse event in 10 FDA reports for BENZOCAINE AND MENTHOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
CHRONIC KIDNEY DISEASE accounts for approximately 1.5% of all adverse event reports for BENZOCAINE AND MENTHOL, making it a notable side effect.
If you experience chronic kidney disease while taking BENZOCAINE AND MENTHOL, 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.