3 reports of this reaction
4.0% of all CAMPHOR AND MENTHOL reports
#4 most reported adverse reaction
ABDOMINAL DISCOMFORT is the #4 most commonly reported adverse reaction for CAMPHOR AND MENTHOL, manufactured by Bayer HealthCare LLC. There are 3 FDA adverse event reports linking CAMPHOR AND MENTHOL to ABDOMINAL DISCOMFORT. This represents approximately 4.0% of all 75 adverse event reports for this drug.
Patients taking CAMPHOR AND MENTHOL who experience abdominal discomfort should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ABDOMINAL DISCOMFORT is moderately reported among CAMPHOR AND MENTHOL users, representing a notable but not dominant share of adverse events.
In addition to abdominal discomfort, the following adverse reactions have been reported for CAMPHOR AND MENTHOL:
The following drugs have also been linked to abdominal discomfort in FDA adverse event reports:
ABDOMINAL DISCOMFORT has been reported as an adverse event in 3 FDA reports for CAMPHOR AND MENTHOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL DISCOMFORT accounts for approximately 4.0% of all adverse event reports for CAMPHOR AND MENTHOL, making it a notable side effect.
If you experience abdominal discomfort while taking CAMPHOR 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.