42 reports of this reaction
3.8% of all MENTHOL, METHYL SALICYLATE reports
#3 most reported adverse reaction
INTENTIONAL PRODUCT MISUSE is the #3 most commonly reported adverse reaction for MENTHOL, METHYL SALICYLATE, manufactured by Hisamitsu Pharmaceutical Co., Inc.. There are 42 FDA adverse event reports linking MENTHOL, METHYL SALICYLATE to INTENTIONAL PRODUCT MISUSE. This represents approximately 3.8% of all 1,107 adverse event reports for this drug.
Patients taking MENTHOL, METHYL SALICYLATE who experience intentional product misuse should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
INTENTIONAL PRODUCT MISUSE is moderately reported among MENTHOL, METHYL SALICYLATE users, representing a notable but not dominant share of adverse events.
In addition to intentional product misuse, the following adverse reactions have been reported for MENTHOL, METHYL SALICYLATE:
The following drugs have also been linked to intentional product misuse in FDA adverse event reports:
INTENTIONAL PRODUCT MISUSE has been reported as an adverse event in 42 FDA reports for MENTHOL, METHYL SALICYLATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
INTENTIONAL PRODUCT MISUSE accounts for approximately 3.8% of all adverse event reports for MENTHOL, METHYL SALICYLATE, making it one of the most commonly reported side effect.
If you experience intentional product misuse while taking MENTHOL, METHYL SALICYLATE, 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.