8 reports of this reaction
1.6% of all CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL reports
#12 most reported adverse reaction
DRY MOUTH is the #12 most commonly reported adverse reaction for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL, manufactured by Procter & Gamble Manufactura S de RL de CV. There are 8 FDA adverse event reports linking CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL to DRY MOUTH. This represents approximately 1.6% of all 485 adverse event reports for this drug.
Patients taking CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL who experience dry mouth should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRY MOUTH is a less commonly reported adverse event for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL, but still significant enough to appear in the safety profile.
In addition to dry mouth, the following adverse reactions have been reported for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL:
The following drugs have also been linked to dry mouth in FDA adverse event reports:
DRY MOUTH has been reported as an adverse event in 8 FDA reports for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRY MOUTH accounts for approximately 1.6% of all adverse event reports for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL, making it a notable side effect.
If you experience dry mouth while taking CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, 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.