5 reports of this reaction
41.7% of all MENTHOL, CAMPHOR reports
#2 most reported adverse reaction
NO ADVERSE EVENT is the #2 most commonly reported adverse reaction for MENTHOL, CAMPHOR, manufactured by Chattem, Inc.. There are 5 FDA adverse event reports linking MENTHOL, CAMPHOR to NO ADVERSE EVENT. This represents approximately 41.7% of all 12 adverse event reports for this drug.
Patients taking MENTHOL, CAMPHOR who experience no adverse event should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NO ADVERSE EVENT is a frequently reported adverse event for MENTHOL, CAMPHOR, accounting for a significant proportion of all reports.
In addition to no adverse event, the following adverse reactions have been reported for MENTHOL, CAMPHOR:
The following drugs have also been linked to no adverse event in FDA adverse event reports:
NO ADVERSE EVENT has been reported as an adverse event in 5 FDA reports for MENTHOL, CAMPHOR. This does not prove causation, but indicates an association observed in post-market surveillance data.
NO ADVERSE EVENT accounts for approximately 41.7% of all adverse event reports for MENTHOL, CAMPHOR, making it one of the most commonly reported side effect.
If you experience no adverse event while taking MENTHOL, CAMPHOR, 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.