CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL

N/A

Manufactured by Procter & Gamble Manufactura S de RL de CV

485 FDA adverse event reports analyzed

Last updated: 2026-04-15

About CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL

CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Procter & Gamble Manufactura S de RL de CV. The most commonly reported adverse reactions for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL include DYSPNOEA, COUGH, DIARRHOEA, DIZZINESS, FATIGUE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL.

Top Adverse Reactions

DYSPNOEA22 reports
COUGH19 reports
DIARRHOEA13 reports
DIZZINESS12 reports
FATIGUE12 reports
HEART RATE INCREASED11 reports
PNEUMONIA11 reports
VOMITING10 reports
EXPOSURE VIA INGESTION9 reports
EXPOSURE VIA INHALATION9 reports
HYPOTENSION9 reports
DRY MOUTH8 reports
OFF LABEL USE8 reports
HEADACHE7 reports
HYPERSENSITIVITY7 reports
NAUSEA7 reports
PRODUCT USE ISSUE7 reports
BLOOD POTASSIUM DECREASED6 reports
DRUG INEFFECTIVE6 reports
DRUG INTERACTION6 reports
FEELING ABNORMAL6 reports
INCORRECT ROUTE OF PRODUCT ADMINISTRATION6 reports
MALAISE6 reports
OXYGEN SATURATION DECREASED6 reports
PNEUMONIA LIPOID6 reports
PRODUCT USE IN UNAPPROVED INDICATION6 reports
SEIZURE6 reports
WEIGHT DECREASED6 reports
ACCIDENTAL EXPOSURE TO PRODUCT BY CHILD5 reports
ASTHENIA5 reports
BLOOD CALCIUM DECREASED5 reports
BLOOD CHLORIDE DECREASED5 reports
CONDITION AGGRAVATED5 reports
CONTUSION5 reports
DEATH5 reports
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE5 reports
DRUG HYPERSENSITIVITY5 reports
INSOMNIA5 reports
NASAL CONGESTION5 reports
PAIN5 reports
PRODUCT ADMINISTERED AT INAPPROPRIATE SITE5 reports
RESPIRATORY RATE INCREASED5 reports
SEPTIC SHOCK5 reports
ABDOMINAL DISCOMFORT4 reports
ARTHRALGIA4 reports
BACK PAIN4 reports
CHEST PAIN4 reports
CONSTIPATION4 reports
DYSPHONIA4 reports
GAIT DISTURBANCE4 reports
PRURITUS4 reports
PYREXIA4 reports
SOMNOLENCE4 reports
TREMOR4 reports
ABDOMINAL PAIN UPPER3 reports
BLOOD CREATININE INCREASED3 reports
BLOOD PRESSURE INCREASED3 reports
CONFUSIONAL STATE3 reports
COVID 193 reports
DEHYDRATION3 reports
DRUG ABUSE3 reports
DYSPEPSIA3 reports
FALL3 reports
HYPOAESTHESIA3 reports
ILLNESS3 reports
INCORRECT ROUTE OF DRUG ADMINISTRATION3 reports
INFLUENZA3 reports
INTENTIONAL PRODUCT MISUSE3 reports
MUSCULAR WEAKNESS3 reports
MYALGIA3 reports
NASOPHARYNGITIS3 reports
OROPHARYNGEAL PAIN3 reports
OVERDOSE3 reports
PAIN IN EXTREMITY3 reports
PARAESTHESIA3 reports
PRODUCT DOSE OMISSION ISSUE3 reports
RASH3 reports
RHINORRHOEA3 reports
SEASONAL ALLERGY3 reports
VISION BLURRED3 reports
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS3 reports
ABDOMINAL PAIN2 reports
ALOPECIA2 reports
BALANCE DISORDER2 reports
BEDRIDDEN2 reports
BLOOD CALCIUM ABNORMAL2 reports
BLOOD POTASSIUM ABNORMAL2 reports
BLOOD UREA INCREASED2 reports
BONE DISORDER2 reports
BRADYCARDIA2 reports
BREATH SOUNDS ABNORMAL2 reports
BRONCHITIS2 reports
CARDIAC FAILURE2 reports
CHEST DISCOMFORT2 reports
CHILLS2 reports
DECREASED APPETITE2 reports
DEPENDENCE2 reports
DRUG DEPENDENCE2 reports
DRUG DOSE OMISSION2 reports
DRUG EFFECT DELAYED2 reports

Report Outcomes

Out of 151 classified reports for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL:

Serious 70.9%Non-Serious 29.1%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female76 (59.4%)
Male51 (39.8%)
Unknown1 (0.8%)

Reports by Age

Age 727 reports
Age 615 reports
Age 675 reports
Age 554 reports
Age 644 reports
Age 684 reports
Age 43 reports
Age 543 reports
Age 743 reports
Age 62 reports
Age 92 reports
Age 232 reports
Age 242 reports
Age 472 reports
Age 562 reports
Age 632 reports
Age 662 reports
Age 702 reports
Age 732 reports
Age 802 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL?

This profile reflects 485 FDA FAERS reports that mention CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL?

Frequently reported terms in FAERS include DYSPNOEA, COUGH, DIARRHOEA, DIZZINESS, FATIGUE, HEART RATE INCREASED. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL?

Labeling and FAERS entries often list Procter & Gamble Manufactura S de RL de CV in connection with CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.