CHILDRENS ACETAMINOPHEN

N/A

Manufactured by AARNA USA INC.

52 FDA adverse event reports analyzed

Last updated: 2026-04-14

About CHILDRENS ACETAMINOPHEN

CHILDRENS ACETAMINOPHEN is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by AARNA USA INC.. The most commonly reported adverse reactions for CHILDRENS ACETAMINOPHEN include ACCIDENTAL EXPOSURE TO PRODUCT BY CHILD, FAILURE OF CHILD RESISTANT MECHANISM FOR PHARMACEUTICAL PRODUCT, OFF LABEL USE, WEIGHT DECREASED, RESPIRATORY SYNCYTIAL VIRUS INFECTION. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CHILDRENS ACETAMINOPHEN.

Top Adverse Reactions

ACCIDENTAL EXPOSURE TO PRODUCT BY CHILD3 reports
FAILURE OF CHILD RESISTANT MECHANISM FOR PHARMACEUTICAL PRODUCT3 reports
OFF LABEL USE3 reports
WEIGHT DECREASED3 reports
RESPIRATORY SYNCYTIAL VIRUS INFECTION2 reports
VOMITING2 reports
ABNORMAL BEHAVIOUR1 reports
ALANINE AMINOTRANSFERASE INCREASED1 reports
ANALGESIC DRUG LEVEL INCREASED1 reports
ASPARTATE AMINOTRANSFERASE INCREASED1 reports
BLOOD METHAEMOGLOBIN PRESENT1 reports
BLOOD PRESSURE DECREASED1 reports
BODY TEMPERATURE DECREASED1 reports
COMA1 reports
COMPLETED SUICIDE1 reports

Report Outcomes

Out of 17 classified reports for CHILDRENS ACETAMINOPHEN:

Serious 29.4%Non-Serious 70.6%

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

Female9 (60.0%)
Male6 (40.0%)

Reports by Age

Age 33 reports
Age 72 reports
Age 11 reports
Age 21 reports
Age 41 reports
Age 61 reports
Age 161 reports
Age 821 reports
Age 4381 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.