LIDOCAINE AND MENTHOL

N/A

Manufactured by Rite Aid Corporation

148 FDA adverse event reports analyzed

Last updated: 2026-04-15

About LIDOCAINE AND MENTHOL

LIDOCAINE AND MENTHOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Rite Aid Corporation. The most commonly reported adverse reactions for LIDOCAINE AND MENTHOL include DRUG INEFFECTIVE, NO ADVERSE EVENT, PAIN, PNEUMONIA, APPLICATION SITE PAIN. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for LIDOCAINE AND MENTHOL.

Top Adverse Reactions

DRUG INEFFECTIVE13 reports
NO ADVERSE EVENT12 reports
PAIN8 reports
PNEUMONIA4 reports
APPLICATION SITE PAIN3 reports
DIZZINESS3 reports
ATRIAL FIBRILLATION2 reports
BACK PAIN2 reports
DISCOMFORT2 reports
DRUG HYPERSENSITIVITY2 reports
DYSPNOEA2 reports
LOCAL SWELLING2 reports
MALAISE2 reports
NAUSEA2 reports
RASH2 reports
RASH ERYTHEMATOUS2 reports
URTICARIA2 reports
ABASIA1 reports
ABDOMINAL DISCOMFORT1 reports
ABDOMINAL PAIN UPPER1 reports
ABSCESS1 reports
ACCIDENT1 reports
ACUTE RESPIRATORY FAILURE1 reports
ALANINE AMINOTRANSFERASE INCREASED1 reports
ANAPHYLACTIC REACTION1 reports
APATHY1 reports
APPLICATION SITE BURN1 reports
APPLICATION SITE DISCOLOURATION1 reports
APPLICATION SITE ERYTHEMA1 reports
APPLICATION SITE RASH1 reports
ARRHYTHMIA1 reports
ARTHRALGIA1 reports
ASPARTATE AMINOTRANSFERASE INCREASED1 reports
BLADDER OPERATION1 reports
BLISTER1 reports
BLOOD PRESSURE DECREASED1 reports
BOWEL MOVEMENT IRREGULARITY1 reports
BURN INFECTION1 reports
CARDIAC FAILURE CONGESTIVE1 reports
CATARACT OPERATION1 reports
CHEMICAL BURN1 reports
CHEST DISCOMFORT1 reports
CHRONIC SINUSITIS1 reports
COLD SWEAT1 reports
COMA1 reports
CONDITION AGGRAVATED1 reports
CONSTIPATION1 reports
CRYING1 reports
DEATH1 reports
DEMENTIA1 reports
DIVERTICULITIS1 reports
DRUG EFFECT LESS THAN EXPECTED1 reports
DRUG INTERACTION1 reports
DYSMENORRHOEA1 reports
DYSURIA1 reports
EAR PAIN1 reports
EPISTAXIS1 reports
ERYTHEMA1 reports
EXPLORATORY OPERATION1 reports
FATIGUE1 reports
FEAR1 reports
FLUSHING1 reports
HEART RATE INCREASED1 reports
HOSPITALISATION1 reports
HYPERHIDROSIS1 reports
HYPERTENSION1 reports
HYPOACUSIS1 reports
HYPOKINESIA1 reports
IMMUNE SYSTEM DISORDER1 reports
INJECTION SITE BRUISING1 reports
INSOMNIA1 reports
KNEE ARTHROPLASTY1 reports
LIMB DISCOMFORT1 reports
LOSS OF CONSCIOUSNESS1 reports
LUNG DISORDER1 reports
MEDICAL DEVICE IMPLANTATION1 reports
MUSCLE STRAIN1 reports
NASOPHARYNGITIS1 reports
NECK PAIN1 reports
NEGATIVE THOUGHTS1 reports
NERVE INJURY1 reports
NEUROPATHY PERIPHERAL1 reports
OEDEMA PERIPHERAL1 reports
OFF LABEL USE1 reports
PHARYNGEAL DISORDER1 reports
POST PROCEDURAL INFECTION1 reports
PRODUCT PACKAGING DIFFICULT TO OPEN1 reports
PRURITUS1 reports
RASH PAPULAR1 reports
RASH PRURITIC1 reports
RESPIRATORY DISORDER1 reports
SCAR1 reports
SECRETION DISCHARGE1 reports
SINUS OPERATION1 reports
SINUSITIS1 reports
SKIN BURNING SENSATION1 reports
SKIN EXFOLIATION1 reports
SPINAL FRACTURE1 reports
SUDDEN HEARING LOSS1 reports
SUICIDAL IDEATION1 reports

Report Outcomes

Out of 60 classified reports for LIDOCAINE AND MENTHOL:

Serious 45.0%Non-Serious 55.0%

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

Female26 (53.1%)
Male23 (46.9%)

Reports by Age

Age 683 reports
Age 512 reports
Age 522 reports
Age 622 reports
Age 702 reports
Age 221 reports
Age 321 reports
Age 451 reports
Age 491 reports
Age 551 reports
Age 561 reports
Age 581 reports
Age 651 reports
Age 691 reports
Age 741 reports
Age 751 reports
Age 811 reports
Age 951 reports
Age 1001 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 AND MENTHOL?

This profile reflects 148 FDA FAERS reports that mention LIDOCAINE AND MENTHOL. Reporting is voluntary and does not prove that the drug caused any listed event.

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

Frequently reported terms in FAERS include DRUG INEFFECTIVE, NO ADVERSE EVENT, PAIN, PNEUMONIA, APPLICATION SITE PAIN, DIZZINESS. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures LIDOCAINE AND MENTHOL?

Labeling and FAERS entries often list Rite Aid Corporation in connection with LIDOCAINE 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.