5% LIDOCAINE

N/A

Manufactured by 100 KARMA INC

31 FDA adverse event reports analyzed

Last updated: 2026-04-15

About 5% LIDOCAINE

5% LIDOCAINE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by 100 KARMA INC. The most commonly reported adverse reactions for 5% LIDOCAINE include PALLOR, ABDOMINAL PAIN, BLOOD PRESSURE DECREASED, CHILLS, CONVULSION. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for 5% LIDOCAINE.

Top Adverse Reactions

PALLOR7 reports
ABDOMINAL PAIN1 reports
BLOOD PRESSURE DECREASED1 reports
CHILLS1 reports
CONVULSION1 reports
DEATH1 reports
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE1 reports
DRUG HYPERSENSITIVITY1 reports
DYSAESTHESIA1 reports
ERYTHEMA1 reports
EYE SWELLING1 reports
FAILURE OF CHILD RESISTANT PRODUCT CLOSURE1 reports
HYPOAESTHESIA1 reports
MYOPATHY1 reports
PRODUCT LABEL CONFUSION1 reports
PRODUCT USE IN UNAPPROVED INDICATION1 reports
RASH1 reports
RHINORRHOEA1 reports
SEIZURE1 reports
SKIN NECROSIS1 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE1 reports
THROAT IRRITATION1 reports
THROAT TIGHTNESS1 reports
TONGUE DISORDER1 reports
TOXICITY TO VARIOUS AGENTS1 reports

Report Outcomes

Out of 17 classified reports for 5% LIDOCAINE:

Serious 64.7%Non-Serious 35.3%

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

Female12 (80.0%)
Male3 (20.0%)

Reports by Age

Age 442 reports
Age 592 reports
Age 31 reports
Age 61 reports
Age 111 reports
Age 451 reports
Age 461 reports
Age 471 reports
Age 481 reports
Age 531 reports
Age 551 reports
Age 751 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 5% LIDOCAINE?

This profile reflects 31 FDA FAERS reports that mention 5% LIDOCAINE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for 5% LIDOCAINE?

Frequently reported terms in FAERS include PALLOR, ABDOMINAL PAIN, BLOOD PRESSURE DECREASED, CHILLS, CONVULSION, DEATH. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures 5% LIDOCAINE?

Labeling and FAERS entries often list 100 KARMA INC in connection with 5% LIDOCAINE. 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.