BENZOCAINE AND MENTHOL

N/A

Manufactured by RB Health (US) LLC

672 FDA adverse event reports analyzed

Last updated: 2026-04-15

About BENZOCAINE AND MENTHOL

BENZOCAINE AND MENTHOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by RB Health (US) LLC. The most commonly reported adverse reactions for BENZOCAINE AND MENTHOL include DYSPNOEA, NAUSEA, DEATH, DIZZINESS, FATIGUE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for BENZOCAINE AND MENTHOL.

Top Adverse Reactions

DYSPNOEA31 reports
NAUSEA19 reports
DEATH16 reports
DIZZINESS15 reports
FATIGUE15 reports
VOMITING15 reports
SEPSIS14 reports
COUGH13 reports
PAIN13 reports
ASTHENIA12 reports
RENAL FAILURE12 reports
HEADACHE11 reports
URINARY TRACT INFECTION11 reports
ACUTE KIDNEY INJURY10 reports
CHRONIC KIDNEY DISEASE10 reports
DEEP VEIN THROMBOSIS10 reports
DIARRHOEA10 reports
PNEUMONIA10 reports
ARTHRALGIA9 reports
CONSTIPATION9 reports
ERYTHEMA9 reports
ABDOMINAL PAIN8 reports
ANAEMIA8 reports
CHEST PAIN8 reports
INSOMNIA8 reports
PULMONARY EMBOLISM8 reports
PYREXIA8 reports
ANXIETY7 reports
BLOOD GLUCOSE INCREASED7 reports
CELLULITIS7 reports
HYPOTENSION7 reports
INFECTION7 reports
SWOLLEN TONGUE7 reports
THROAT TIGHTNESS7 reports
ACUTE RESPIRATORY FAILURE6 reports
CEREBROVASCULAR ACCIDENT6 reports
DECREASED APPETITE6 reports
END STAGE RENAL DISEASE6 reports
FALL6 reports
HAEMOGLOBIN DECREASED6 reports
HYPERHIDROSIS6 reports
HYPERTENSION6 reports
INJURY6 reports
NASOPHARYNGITIS6 reports
OROPHARYNGEAL PAIN6 reports
PAIN IN EXTREMITY6 reports
PALPITATIONS6 reports
WEIGHT INCREASED6 reports
CARDIO RESPIRATORY ARREST5 reports
DEPRESSION5 reports
DYSPHAGIA5 reports
DYSPHONIA5 reports
FEBRILE NEUTROPENIA5 reports
FEELING ABNORMAL5 reports
HYPERPARATHYROIDISM SECONDARY5 reports
LIP SWELLING5 reports
MUSCLE SPASMS5 reports
NASAL CONGESTION5 reports
NECROTISING FASCIITIS5 reports
NEPHROGENIC ANAEMIA5 reports
RASH5 reports
SWELLING FACE5 reports
URTICARIA5 reports
VISION BLURRED5 reports
AMNESIA4 reports
BURNING SENSATION4 reports
CARDIAC DISORDER4 reports
CONDITION AGGRAVATED4 reports
COVID 194 reports
DRUG INEFFECTIVE4 reports
DYSPNOEA EXERTIONAL4 reports
DYSURIA4 reports
EMOTIONAL DISTRESS4 reports
FOURNIER^S GANGRENE4 reports
GAIT DISTURBANCE4 reports
GASTROINTESTINAL HAEMORRHAGE4 reports
HEART RATE INCREASED4 reports
HYPOAESTHESIA4 reports
HYPOXIA4 reports
JOINT SWELLING4 reports
MALAISE4 reports
MEMORY IMPAIRMENT4 reports
MYALGIA4 reports
OEDEMA PERIPHERAL4 reports
OFF LABEL USE4 reports
PHARYNGEAL OEDEMA4 reports
PRODUCTIVE COUGH4 reports
PRURITUS4 reports
RESPIRATORY FAILURE4 reports
TACHYCARDIA4 reports
THROAT IRRITATION4 reports
THROMBOCYTOPENIA4 reports
UNRESPONSIVE TO STIMULI4 reports
ABDOMINAL DISCOMFORT3 reports
ABDOMINAL PAIN UPPER3 reports
ABSCESS LIMB3 reports
AGITATION3 reports
ANAL ABSCESS3 reports
BALANCE DISORDER3 reports
BRONCHITIS3 reports

Report Outcomes

Out of 250 classified reports for BENZOCAINE AND MENTHOL:

Serious 84.0%Non-Serious 16.0%

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

Female152 (61.8%)
Male93 (37.8%)
Unknown1 (0.4%)

Reports by Age

Age 587 reports
Age 696 reports
Age 746 reports
Age 766 reports
Age 155 reports
Age 455 reports
Age 615 reports
Age 635 reports
Age 675 reports
Age 715 reports
Age 304 reports
Age 314 reports
Age 474 reports
Age 504 reports
Age 564 reports
Age 684 reports
Age 704 reports
Age 754 reports
Age 774 reports
Age 343 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 BENZOCAINE AND MENTHOL?

This profile reflects 672 FDA FAERS reports that mention BENZOCAINE AND MENTHOL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for BENZOCAINE AND MENTHOL?

Frequently reported terms in FAERS include DYSPNOEA, NAUSEA, DEATH, DIZZINESS, FATIGUE, VOMITING. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures BENZOCAINE AND MENTHOL?

Labeling and FAERS entries often list RB Health (US) LLC in connection with BENZOCAINE 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.