160 reports of this reaction
10.0% of all CAMPHOR, MENTHOL reports
#2 most reported adverse reaction
NO ADVERSE EVENT is the #2 most commonly reported adverse reaction for CAMPHOR, MENTHOL, manufactured by Chattem, Inc.. There are 160 FDA adverse event reports linking CAMPHOR, MENTHOL to NO ADVERSE EVENT. This represents approximately 10.0% of all 1,597 adverse event reports for this drug.
Patients taking CAMPHOR, MENTHOL 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 moderately reported among CAMPHOR, MENTHOL users, representing a notable but not dominant share of adverse events.
In addition to no adverse event, the following adverse reactions have been reported for CAMPHOR, MENTHOL:
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 160 FDA reports for CAMPHOR, MENTHOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
NO ADVERSE EVENT accounts for approximately 10.0% of all adverse event reports for CAMPHOR, MENTHOL, making it one of the most commonly reported side effect.
If you experience no adverse event while taking CAMPHOR, 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.