LIDOCAINE HCL, MENTHOL

N/A

Manufactured by Amazon.com Services LLC

208 FDA adverse event reports analyzed

Last updated: 2026-04-15

About LIDOCAINE HCL, MENTHOL

LIDOCAINE HCL, MENTHOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Amazon.com Services LLC. The most commonly reported adverse reactions for LIDOCAINE HCL, MENTHOL include FATIGUE, NAUSEA, DIARRHOEA, ERYTHEMA, PARAESTHESIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for LIDOCAINE HCL, MENTHOL.

Top Adverse Reactions

FATIGUE7 reports
NAUSEA5 reports
DIARRHOEA4 reports
ERYTHEMA4 reports
PARAESTHESIA4 reports
PRURITUS4 reports
RASH4 reports
CHEST PAIN3 reports
COGNITIVE DISORDER3 reports
DISTURBANCE IN ATTENTION3 reports
DRY SKIN3 reports
DYSPEPSIA3 reports
DYSPNOEA3 reports
FEELING ABNORMAL3 reports
HALLUCINATION3 reports
HYPERSENSITIVITY3 reports
HYPOAESTHESIA3 reports
MENTAL IMPAIRMENT3 reports
MUSCULAR WEAKNESS3 reports
MYALGIA3 reports
PAIN3 reports
PAIN IN EXTREMITY3 reports
PANIC ATTACK3 reports
VISUAL IMPAIRMENT3 reports
VOMITING3 reports
ABASIA2 reports
ABDOMINAL DISTENSION2 reports
ANAEMIA2 reports
ANXIETY2 reports
ARTHRALGIA2 reports
ASTHENIA2 reports
BALANCE DISORDER2 reports
BODY TEMPERATURE DECREASED2 reports
CHEST DISCOMFORT2 reports
CONSTIPATION2 reports
COUGH2 reports
DEVICE FAILURE2 reports
DEVICE ISSUE2 reports
DIZZINESS2 reports
EJECTION FRACTION DECREASED2 reports
EPISTAXIS2 reports
EXTRASYSTOLES2 reports
FEELING HOT2 reports
FLATULENCE2 reports
GAIT DISTURBANCE2 reports
HEART RATE IRREGULAR2 reports
HOSPITALISATION2 reports
HYPERVENTILATION2 reports
IMPAIRED GASTRIC EMPTYING2 reports
INSOMNIA2 reports
LIVER FUNCTION TEST ABNORMAL2 reports
LYMPHOEDEMA2 reports
MALAISE2 reports
MEMORY IMPAIRMENT2 reports
MIDDLE INSOMNIA2 reports
MOVEMENT DISORDER2 reports
MUSCLE SPASMS2 reports
MUSCLE TIGHTNESS2 reports
MUSCULOSKELETAL DISCOMFORT2 reports
MUSCULOSKELETAL PAIN2 reports
NASAL CONGESTION2 reports
NASAL ULCER2 reports
NEUROPATHY PERIPHERAL2 reports
ONYCHALGIA2 reports
PALMAR ERYTHEMA2 reports
RENAL FUNCTION TEST ABNORMAL2 reports
SOMNOLENCE2 reports
SPEECH DISORDER2 reports
TENSION2 reports
THYROID FUNCTION TEST ABNORMAL2 reports
WEIGHT INCREASED2 reports
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS2 reports
ABDOMINAL DISCOMFORT1 reports
ABDOMINAL INFECTION1 reports
ABDOMINAL PAIN1 reports
ABDOMINAL PAIN UPPER1 reports
ACNE1 reports
ADVERSE EVENT1 reports
ALOPECIA1 reports
AMNESIA1 reports
APPLICATION SITE PAIN1 reports
APPLICATION SITE PRURITUS1 reports
APPLICATION SITE RASH1 reports
BACK PAIN1 reports
BLOOD LACTATE DEHYDROGENASE1 reports
BLOOD LACTATE DEHYDROGENASE INCREASED1 reports
BLOOD PRESSURE INCREASED1 reports
BUTTOCK INJURY1 reports
CARDIAC ARREST1 reports
CHEMICAL BURN1 reports
COLD SWEAT1 reports
CONFUSIONAL STATE1 reports
CONSCIOUSNESS FLUCTUATING1 reports
DEATH1 reports
DECREASED INTEREST1 reports
DEHYDRATION1 reports
DELIRIUM1 reports
DEMENTIA1 reports
DEPRESSED MOOD1 reports
DEVICE ALARM ISSUE1 reports

Report Outcomes

Out of 33 classified reports for LIDOCAINE HCL, MENTHOL:

Serious 66.7%Non-Serious 33.3%

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

Female22 (68.8%)
Male10 (31.3%)

Reports by Age

Age 523 reports
Age 352 reports
Age 562 reports
Age 592 reports
Age 602 reports
Age 622 reports
Age 642 reports
Age 361 reports
Age 371 reports
Age 491 reports
Age 501 reports
Age 551 reports
Age 611 reports
Age 651 reports
Age 691 reports
Age 701 reports
Age 711 reports
Age 751 reports
Age 771 reports
Age 851 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 LIDOCAINE HCL, MENTHOL?

This profile reflects 208 FDA FAERS reports that mention LIDOCAINE HCL, MENTHOL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for LIDOCAINE HCL, MENTHOL?

Frequently reported terms in FAERS include FATIGUE, NAUSEA, DIARRHOEA, ERYTHEMA, PARAESTHESIA, PRURITUS. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures LIDOCAINE HCL, MENTHOL?

Labeling and FAERS entries often list Amazon.com Services LLC in connection with LIDOCAINE HCL, 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.