CHILDRENS PAIN RELIEF

N/A

Manufactured by Allegiant Health

50 FDA adverse event reports analyzed

Last updated: 2026-04-14

About CHILDRENS PAIN RELIEF

CHILDRENS PAIN RELIEF is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Allegiant Health. The most commonly reported adverse reactions for CHILDRENS PAIN RELIEF include WEIGHT INCREASED, OFF LABEL USE, PRODUCT DOSE OMISSION ISSUE, WEIGHT DECREASED, ACUTE KIDNEY INJURY. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CHILDRENS PAIN RELIEF.

Top Adverse Reactions

WEIGHT INCREASED3 reports
OFF LABEL USE2 reports
PRODUCT DOSE OMISSION ISSUE2 reports
WEIGHT DECREASED2 reports
ACUTE KIDNEY INJURY1 reports
ALANINE AMINOTRANSFERASE INCREASED1 reports
ASPARTATE AMINOTRANSFERASE INCREASED1 reports
BODY TEMPERATURE INCREASED1 reports
CARDIAC VALVE DISEASE1 reports
CATHETER SITE INFECTION1 reports
COUGH1 reports
DYSPNOEA1 reports
EAR HAEMORRHAGE1 reports
FAILURE TO THRIVE1 reports
GASTROINTESTINAL TUBE INSERTION1 reports
GASTROSTOMY1 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION1 reports
INCORRECT DOSE ADMINISTERED1 reports
INFLUENZA1 reports
LIVER FUNCTION TEST ABNORMAL1 reports
MATERNAL EXPOSURE DURING PREGNANCY1 reports
MUCOSAL DISCOLOURATION1 reports
MULTIPLE ORGAN DYSFUNCTION SYNDROME1 reports
MUSCULAR WEAKNESS1 reports
NASOPHARYNGITIS1 reports
OESOPHAGOGASTRIC FUNDOPLASTY1 reports
ORTHOPAEDIC PROCEDURE1 reports
PALLOR1 reports
PANCREATITIS1 reports
PARAINFLUENZAE VIRUS INFECTION1 reports
PERICARDIAL EFFUSION1 reports
PNEUMONIA1 reports
PNEUMONIA ASPIRATION1 reports
PYREXIA1 reports
RASH1 reports
RESPIRATORY DISTRESS1 reports
RESPIRATORY TRACT INFECTION VIRAL1 reports
RETCHING1 reports
SERRATIA INFECTION1 reports
SINUSITIS1 reports
TRACHEITIS1 reports
TRACHEOSTOMY1 reports
UPPER RESPIRATORY TRACT INFECTION BACTERIAL1 reports
URTICARIA1 reports
VOMITING1 reports

Report Outcomes

Out of 16 classified reports for CHILDRENS PAIN RELIEF:

Serious 56.3%Non-Serious 43.8%

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

Male7 (50.0%)
Female7 (50.0%)

Reports by Age

Age 22 reports
Age 11 reports
Age 61 reports
Age 71 reports
Age 91 reports
Age 121 reports
Age 141 reports
Age 151 reports
Age 641 reports
Age 711 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 CHILDRENS PAIN RELIEF?

This profile reflects 50 FDA FAERS reports that mention CHILDRENS PAIN RELIEF. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CHILDRENS PAIN RELIEF?

Frequently reported terms in FAERS include WEIGHT INCREASED, OFF LABEL USE, PRODUCT DOSE OMISSION ISSUE, WEIGHT DECREASED, ACUTE KIDNEY INJURY, ALANINE AMINOTRANSFERASE INCREASED. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures CHILDRENS PAIN RELIEF?

Labeling and FAERS entries often list Allegiant Health in connection with CHILDRENS PAIN RELIEF. 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.