MECLIZINE

N/A

Manufactured by Advanced Rx LLC

38,863 FDA adverse event reports analyzed

Last updated: 2026-04-14

About MECLIZINE

MECLIZINE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Advanced Rx LLC. The most commonly reported adverse reactions for MECLIZINE include DIZZINESS, NAUSEA, FATIGUE, HEADACHE, DIARRHOEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for MECLIZINE.

Top Adverse Reactions

DIZZINESS1,567 reports
NAUSEA1,350 reports
FATIGUE1,303 reports
HEADACHE1,010 reports
DIARRHOEA991 reports
PAIN984 reports
FALL964 reports
DYSPNOEA851 reports
CHRONIC KIDNEY DISEASE839 reports
ASTHENIA793 reports
DRUG INEFFECTIVE734 reports
VOMITING691 reports
RENAL FAILURE637 reports
ANXIETY609 reports
VERTIGO606 reports

Report Outcomes

Out of 15,600 classified reports for MECLIZINE:

Serious 63.1%Non-Serious 36.9%

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

Female10,928 (74.1%)
Male3,804 (25.8%)
Unknown10 (0.1%)

Reports by Age

Age 63268 reports
Age 65263 reports
Age 71262 reports
Age 74259 reports
Age 69246 reports
Age 66238 reports
Age 64231 reports
Age 67228 reports
Age 70228 reports
Age 73226 reports
Age 75226 reports
Age 68224 reports
Age 72215 reports
Age 78215 reports
Age 62214 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.