2 reports of this reaction
2.7% of all CAMPHOR AND MENTHOL reports
#9 most reported adverse reaction
HAEMORRHAGE is the #9 most commonly reported adverse reaction for CAMPHOR AND MENTHOL, manufactured by Bayer HealthCare LLC. There are 2 FDA adverse event reports linking CAMPHOR AND MENTHOL to HAEMORRHAGE. This represents approximately 2.7% of all 75 adverse event reports for this drug.
Patients taking CAMPHOR AND MENTHOL who experience haemorrhage should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HAEMORRHAGE is a less commonly reported adverse event for CAMPHOR AND MENTHOL, but still significant enough to appear in the safety profile.
In addition to haemorrhage, the following adverse reactions have been reported for CAMPHOR AND MENTHOL:
The following drugs have also been linked to haemorrhage in FDA adverse event reports:
HAEMORRHAGE has been reported as an adverse event in 2 FDA reports for CAMPHOR AND MENTHOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
HAEMORRHAGE accounts for approximately 2.7% of all adverse event reports for CAMPHOR AND MENTHOL, making it a notable side effect.
If you experience haemorrhage 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.