MECLIZINE HCL

N/A

Manufactured by Rising Pharma Holdings, Inc.

4,811 FDA adverse event reports analyzed

Last updated: 2026-04-15

About MECLIZINE HCL

MECLIZINE HCL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Rising Pharma Holdings, Inc.. The most commonly reported adverse reactions for MECLIZINE HCL include FATIGUE, DIZZINESS, DRUG INEFFECTIVE, FALL, NAUSEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for MECLIZINE HCL.

Top Adverse Reactions

FATIGUE196 reports
DIZZINESS191 reports
DRUG INEFFECTIVE166 reports
FALL163 reports
NAUSEA160 reports
DIARRHOEA131 reports
HEADACHE127 reports
PAIN113 reports
ASTHENIA105 reports
DEATH105 reports
GAIT DISTURBANCE82 reports
MALAISE81 reports
VOMITING77 reports
DYSPNOEA73 reports
DEPRESSION71 reports

Report Outcomes

Out of 2,181 classified reports for MECLIZINE HCL:

Serious 51.9%Non-Serious 48.1%

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

Female1,496 (72.6%)
Male563 (27.3%)
Unknown1 (0.0%)

Reports by Age

Age 5840 reports
Age 7338 reports
Age 6637 reports
Age 7037 reports
Age 6936 reports
Age 6534 reports
Age 7734 reports
Age 7232 reports
Age 7632 reports
Age 5730 reports
Age 7130 reports
Age 7530 reports
Age 7427 reports
Age 8227 reports
Age 5526 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.