LIDOCAINE HYDROCHLORIDE, MENTHOL

N/A

Manufactured by ANI Pharmaceuticals, Inc.

30 FDA adverse event reports analyzed

Last updated: 2026-04-15

About LIDOCAINE HYDROCHLORIDE, MENTHOL

LIDOCAINE HYDROCHLORIDE, MENTHOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by ANI Pharmaceuticals, Inc.. The most commonly reported adverse reactions for LIDOCAINE HYDROCHLORIDE, MENTHOL include ABDOMINAL PAIN UPPER, BLOOD CHOLESTEROL INCREASED, CONSTIPATION, COVID-19 PNEUMONIA, DIARRHOEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for LIDOCAINE HYDROCHLORIDE, MENTHOL.

Top Adverse Reactions

ABDOMINAL PAIN UPPER1 reports
BLOOD CHOLESTEROL INCREASED1 reports
CONSTIPATION1 reports
COVID 19 PNEUMONIA1 reports
DIARRHOEA1 reports
DRUG INEFFECTIVE1 reports
DRUG INTERACTION1 reports
DRY MOUTH1 reports
ERYTHEMA1 reports
FLATULENCE1 reports
GASTROINTESTINAL DISORDER1 reports
GASTROINTESTINAL SOUNDS ABNORMAL1 reports
GROIN PAIN1 reports
INSOMNIA1 reports
JOINT LOCK1 reports
MICTURITION URGENCY1 reports
NAUSEA1 reports
NERVOUSNESS1 reports
NEURALGIA1 reports
NOCTURIA1 reports
ORCHITIS NONINFECTIVE1 reports
PAIN IN EXTREMITY1 reports
PROSTATIC DISORDER1 reports
PRURITUS1 reports
SKIN DISORDER1 reports
STRESS1 reports
URETHRAL STENOSIS1 reports
VOMITING1 reports
WEIGHT DECREASED1 reports
WHEEZING1 reports

Report Outcomes

Out of 3 classified reports for LIDOCAINE HYDROCHLORIDE, 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

Male2 (66.7%)
Female1 (33.3%)

Reports by Age

Age 871 reports
Age 207181 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 HYDROCHLORIDE, MENTHOL?

This profile reflects 30 FDA FAERS reports that mention LIDOCAINE HYDROCHLORIDE, MENTHOL. Reporting is voluntary and does not prove that the drug caused any listed event.

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

Frequently reported terms in FAERS include ABDOMINAL PAIN UPPER, BLOOD CHOLESTEROL INCREASED, CONSTIPATION, COVID-19 PNEUMONIA, DIARRHOEA, DRUG INEFFECTIVE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures LIDOCAINE HYDROCHLORIDE, MENTHOL?

Labeling and FAERS entries often list ANI Pharmaceuticals, Inc. in connection with LIDOCAINE HYDROCHLORIDE, 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.