HELIUM

N/A

Manufactured by A-OX Welding Supply, LLC

129 FDA adverse event reports analyzed

Last updated: 2026-04-15

About HELIUM

HELIUM is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by A-OX Welding Supply, LLC. The most commonly reported adverse reactions for HELIUM include COMPLETED SUICIDE, ASPHYXIA, OVERDOSE, TOXICITY TO VARIOUS AGENTS, GENERALISED TONIC-CLONIC SEIZURE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for HELIUM.

Top Adverse Reactions

COMPLETED SUICIDE23 reports
ASPHYXIA6 reports
OVERDOSE6 reports
TOXICITY TO VARIOUS AGENTS5 reports
GENERALISED TONIC CLONIC SEIZURE4 reports
SEDATION4 reports
DRUG LEVEL INCREASED3 reports
MYALGIA3 reports
OFF LABEL USE3 reports
ABNORMAL BEHAVIOUR2 reports
AGGRESSION2 reports
CATAPLEXY2 reports
DEATH2 reports
DEPRESSION2 reports
DIARRHOEA2 reports
DRUG INEFFECTIVE2 reports
ECZEMA2 reports
EXPOSURE VIA INGESTION2 reports
GAS POISONING2 reports
INSOMNIA2 reports
INTENTIONAL PRODUCT MISUSE2 reports
IRRITABILITY2 reports
LOSS OF CONSCIOUSNESS2 reports
PARANOIA2 reports
PERSONALITY CHANGE2 reports
SPINAL FRACTURE2 reports
AMNESIA1 reports
ASCITES1 reports
CARDIAC FAILURE CONGESTIVE1 reports
CEREBRAL GAS EMBOLISM1 reports
COMA1 reports
CONTRAINDICATED PRODUCT ADMINISTERED1 reports
CREPITATIONS1 reports
DEAFNESS1 reports
DYSPNOEA1 reports
EMPHYSEMA1 reports
EXPOSURE VIA INHALATION1 reports
FALL1 reports
HOMICIDE1 reports
HYPERCAPNIA1 reports
HYPERVOLAEMIA1 reports
HYPOACUSIS1 reports
IMPATIENCE1 reports
INTENTIONAL DRUG MISUSE1 reports
INTENTIONAL OVERDOSE1 reports
MEMORY IMPAIRMENT1 reports
MENTAL STATUS CHANGES1 reports
METABOLIC ACIDOSIS1 reports
MULTI ORGAN FAILURE1 reports
MYOPATHY1 reports
NEUTROPENIA1 reports
PNEUMOTHORAX1 reports
PRODUCT LABEL ON WRONG PRODUCT1 reports
RENAL FAILURE1 reports
RESPIRATORY DISORDER1 reports
SEASONAL ALLERGY1 reports
SKIN IRRITATION1 reports
SLEEP DISORDER1 reports
SOMNOLENCE1 reports
SUBCUTANEOUS EMPHYSEMA1 reports
SUICIDE ATTEMPT1 reports
VICTIM OF HOMICIDE1 reports
WEIGHT INCREASED1 reports
WRONG DRUG ADMINISTERED1 reports

Report Outcomes

Out of 50 classified reports for HELIUM:

Serious 92.0%Non-Serious 8.0%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Frequently Asked Questions

How many FDA adverse event reports are associated with HELIUM?

This profile reflects 129 FDA FAERS reports that mention HELIUM. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for HELIUM?

Frequently reported terms in FAERS include COMPLETED SUICIDE, ASPHYXIA, OVERDOSE, TOXICITY TO VARIOUS AGENTS, GENERALISED TONIC-CLONIC SEIZURE, SEDATION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures HELIUM?

Labeling and FAERS entries often list A-OX Welding Supply, LLC in connection with HELIUM. 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.