12 reports of this reaction
2.5% of all CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL reports
#4 most reported adverse reaction
DIZZINESS is the #4 most commonly reported adverse reaction for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL, manufactured by Procter & Gamble Manufactura S de RL de CV. There are 12 FDA adverse event reports linking CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL to DIZZINESS. This represents approximately 2.5% of all 485 adverse event reports for this drug.
Patients taking CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL who experience dizziness should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIZZINESS 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 dizziness, the following adverse reactions have been reported for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL:
The following drugs have also been linked to dizziness in FDA adverse event reports:
DIZZINESS has been reported as an adverse event in 12 FDA reports for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIZZINESS accounts for approximately 2.5% of all adverse event reports for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL, making it a notable side effect.
If you experience dizziness 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.