IVERMECTIN

N/A

Manufactured by Merck Sharp & Dohme LLC

12,395 FDA adverse event reports analyzed

Last updated: 2026-04-15

About IVERMECTIN

IVERMECTIN is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Merck Sharp & Dohme LLC. The most commonly reported adverse reactions for IVERMECTIN include DRUG INEFFECTIVE, HEADACHE, ASTHENIA, PYREXIA, OFF LABEL USE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for IVERMECTIN.

Top Adverse Reactions

DRUG INEFFECTIVE728 reports
HEADACHE635 reports
ASTHENIA588 reports
PYREXIA484 reports
OFF LABEL USE463 reports
PRODUCT USE IN UNAPPROVED INDICATION445 reports
PRURITUS374 reports
DIARRHOEA286 reports
OCULAR HYPERAEMIA255 reports
COMA246 reports
CONJUNCTIVAL HAEMORRHAGE238 reports
ERYTHEMA237 reports
BACK PAIN225 reports
VERTIGO218 reports
ARTHRALGIA203 reports

Report Outcomes

Out of 5,936 classified reports for IVERMECTIN:

Serious 58.9%Non-Serious 41.1%

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

Female2,666 (52.4%)
Male2,393 (47.0%)
Unknown31 (0.6%)

Reports by Age

Age 6496 reports
Age 5688 reports
Age 5485 reports
Age 6084 reports
Age 6578 reports
Age 4077 reports
Age 4677 reports
Age 4275 reports
Age 4475 reports
Age 6274 reports
Age 6172 reports
Age 5871 reports
Age 6371 reports
Age 6870 reports
Age 4769 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

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.