NITROUS OXIDE

N/A

Manufactured by AGL Welding Supply Co., Inc.

3,365 FDA adverse event reports analyzed

Last updated: 2026-04-15

About NITROUS OXIDE

NITROUS OXIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by AGL Welding Supply Co., Inc.. The most commonly reported adverse reactions for NITROUS OXIDE include DRUG ABUSE, DRUG INTERACTION, CARDIAC ARREST, ANAESTHETIC COMPLICATION NEUROLOGICAL, BRADYCARDIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for NITROUS OXIDE.

Top Adverse Reactions

DRUG ABUSE135 reports
DRUG INTERACTION133 reports
CARDIAC ARREST121 reports
ANAESTHETIC COMPLICATION NEUROLOGICAL117 reports
BRADYCARDIA102 reports
HYPOTENSION93 reports
SUBACUTE COMBINED CORD DEGENERATION84 reports
TOXICITY TO VARIOUS AGENTS81 reports
OFF LABEL USE66 reports
DRUG INEFFECTIVE64 reports
HYPERTHERMIA MALIGNANT53 reports
VOMITING48 reports
SUBSTANCE USE47 reports
PARAESTHESIA46 reports
CHOROIDAL INFARCTION45 reports
NAUSEA45 reports
PULMONARY OEDEMA45 reports
VENTRICULAR TACHYCARDIA44 reports
VITAMIN B12 DEFICIENCY44 reports
DRUG DEPENDENCE43 reports
VENTRICULAR FIBRILLATION43 reports
OXYGEN SATURATION DECREASED40 reports
HYPOXIA39 reports
ANAESTHETIC COMPLICATION38 reports
TACHYCARDIA38 reports
SOMNOLENCE37 reports
AGITATION36 reports
ANAPHYLACTIC REACTION36 reports
FOETAL EXPOSURE DURING PREGNANCY36 reports
HYPERTENSION35 reports
DEPRESSED LEVEL OF CONSCIOUSNESS34 reports
APNOEA33 reports
INTENTIONAL PRODUCT MISUSE32 reports
SINUS TACHYCARDIA32 reports
SEIZURE31 reports
HYPERKALAEMIA30 reports
MYELOPATHY30 reports
MUSCULAR WEAKNESS28 reports
BLOOD PRESSURE DECREASED27 reports
LARYNGOSPASM27 reports
RESPIRATORY DEPRESSION27 reports
MATERNAL EXPOSURE DURING PREGNANCY26 reports
PULMONARY EMBOLISM26 reports
PYREXIA26 reports
DRUG USE DISORDER25 reports
ELECTROCARDIOGRAM QT PROLONGED25 reports
EXPOSURE DURING PREGNANCY25 reports
GAIT DISTURBANCE25 reports
HEADACHE25 reports
CONFUSIONAL STATE24 reports
DELAYED RECOVERY FROM ANAESTHESIA24 reports
PAIN24 reports
RESPIRATORY FAILURE24 reports
ERYTHEMA23 reports
LEUKOENCEPHALOPATHY23 reports
LOSS OF CONSCIOUSNESS23 reports
METABOLIC ACIDOSIS23 reports
NEUROPATHY PERIPHERAL23 reports
BRAIN OEDEMA22 reports
CARDIO RESPIRATORY ARREST22 reports
OVERDOSE22 reports
PREMATURE BABY22 reports
RESPIRATORY ARREST22 reports
ANXIETY21 reports
CONDITION AGGRAVATED21 reports
CYANOSIS21 reports
DRUG EXPOSURE DURING PREGNANCY21 reports
DRUG HYPERSENSITIVITY21 reports
HEART RATE DECREASED21 reports
LIPODYSTROPHY ACQUIRED21 reports
AGGRESSION20 reports
ANAPHYLACTIC SHOCK20 reports
HYPOAESTHESIA20 reports
PROCEDURAL COMPLICATION20 reports
RHABDOMYOLYSIS20 reports
SEROTONIN SYNDROME20 reports
DYSPNOEA19 reports
DYSTONIA19 reports
HALLUCINATION, VISUAL19 reports
RESPIRATORY DISTRESS19 reports
SUBSTANCE ABUSER19 reports
VITAMIN B12 DECREASED19 reports
ATAXIA18 reports
HEART RATE INCREASED18 reports
POLYNEUROPATHY18 reports
UNRESPONSIVE TO STIMULI18 reports
BRONCHOSPASM17 reports
DRUG INDUCED LIVER INJURY17 reports
PNEUMONIA17 reports
ANAEMIA16 reports
DEEP VEIN THROMBOSIS16 reports
NEUROMUSCULAR BLOCK PROLONGED16 reports
POST PROCEDURAL COMPLICATION16 reports
PROCEDURAL NAUSEA16 reports
PROCEDURAL VOMITING16 reports
SEPSIS16 reports
APHASIA15 reports
CAESAREAN SECTION15 reports
CARDIOGENIC SHOCK15 reports
COMPLETED SUICIDE15 reports

Report Outcomes

Out of 2,114 classified reports for NITROUS OXIDE:

Serious 93.9%Non-Serious 6.1%

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

Male916 (50.0%)
Female883 (48.2%)
Unknown32 (1.7%)

Reports by Age

Age 2254 reports
Age 2554 reports
Age 2051 reports
Age 1949 reports
Age 1847 reports
Age 1645 reports
Age 1743 reports
Age 438 reports
Age 2138 reports
Age 1337 reports
Age 734 reports
Age 2431 reports
Age 3031 reports
Age 330 reports
Age 2329 reports
Age 1228 reports
Age 2627 reports
Age 5527 reports
Age 526 reports
Age 2726 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 NITROUS OXIDE?

This profile reflects 3,365 FDA FAERS reports that mention NITROUS OXIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for NITROUS OXIDE?

Frequently reported terms in FAERS include DRUG ABUSE, DRUG INTERACTION, CARDIAC ARREST, ANAESTHETIC COMPLICATION NEUROLOGICAL, BRADYCARDIA, HYPOTENSION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures NITROUS OXIDE?

Labeling and FAERS entries often list AGL Welding Supply Co., Inc. in connection with NITROUS OXIDE. 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.