CARBON DIOXIDE

N/A

Manufactured by A-OX Welding Supply, LLC

267 FDA adverse event reports analyzed

Last updated: 2026-04-15

About CARBON DIOXIDE

CARBON DIOXIDE 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 CARBON DIOXIDE include AIR EMBOLISM, SUBCUTANEOUS EMPHYSEMA, OFF LABEL USE, POST PROCEDURAL COMPLICATION, CARDIAC ARREST. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CARBON DIOXIDE.

Top Adverse Reactions

AIR EMBOLISM32 reports
SUBCUTANEOUS EMPHYSEMA20 reports
OFF LABEL USE16 reports
POST PROCEDURAL COMPLICATION9 reports
CARDIAC ARREST8 reports
HYPOTENSION7 reports
PNEUMOPERITONEUM7 reports
DRUG ADMINISTRATION ERROR5 reports
HYPERCAPNIA5 reports
PCO2 INCREASED5 reports
PNEUMOMEDIASTINUM5 reports
INTESTINAL ISCHAEMIA4 reports
RESPIRATORY ACIDOSIS4 reports
TACHYCARDIA4 reports
ATELECTASIS3 reports
CEREBRAL GAS EMBOLISM3 reports
GENERAL PHYSICAL HEALTH DETERIORATION3 reports
NAUSEA3 reports
PARADOXICAL EMBOLISM3 reports
PNEUMONIA3 reports
PYREXIA3 reports
ABDOMINAL DISTENSION2 reports
ABDOMINAL SEPSIS2 reports
ACIDOSIS2 reports
ANXIETY2 reports
ARRHYTHMIA2 reports
ARTHRALGIA2 reports
BRADYCARDIA2 reports
CHILLS2 reports
CIRCULATORY COLLAPSE2 reports
COLITIS ISCHAEMIC2 reports
DISCOMFORT2 reports
DYSPHAGIA2 reports
ELECTROCARDIOGRAM ST SEGMENT ELEVATION2 reports
ERYTHEMA2 reports
HAEMODYNAMIC INSTABILITY2 reports
HYPOXIA2 reports
INTESTINAL INFARCTION2 reports
INTESTINAL PERFORATION2 reports
LARGE INTESTINE PERFORATION2 reports
MALAISE2 reports
MEDICATION ERROR2 reports
MENTAL DISORDER2 reports
MULTIPLE ORGAN DYSFUNCTION SYNDROME2 reports
MUSCULOSKELETAL PAIN2 reports
PAIN IN EXTREMITY2 reports
PITUITARY HAEMORRHAGE2 reports
RASH2 reports
RASH PRURITIC2 reports
RENAL FAILURE2 reports
RETCHING2 reports
SKIN DISORDER2 reports
STRESS2 reports
STRESS CARDIOMYOPATHY2 reports
URTICARIA2 reports
VENTRICULAR TACHYCARDIA2 reports
VOMITING2 reports
ABDOMINAL ADHESIONS1 reports
ABDOMINAL DISCOMFORT1 reports
ABDOMINAL PAIN1 reports
ABDOMINAL PAIN LOWER1 reports
ABDOMINAL PAIN UPPER1 reports
ACCIDENTAL EXPOSURE TO PRODUCT1 reports
ACTIVITIES OF DAILY LIVING IMPAIRED1 reports
ACUTE ABDOMEN1 reports
ACUTE RESPIRATORY DISTRESS SYNDROME1 reports
AMYLASE INCREASED1 reports
ANAEMIA1 reports
ANAESTHETIC COMPLICATION NEUROLOGICAL1 reports
ANAESTHETIC COMPLICATION PULMONARY1 reports
ANOXIC ENCEPHALOPATHY1 reports
ARTERIAL HAEMORRHAGE1 reports
ARTHRITIS1 reports
ASCITES1 reports
ASPARTATE AMINOTRANSFERASE INCREASED1 reports
ASPHYXIA1 reports
ASTHMA1 reports
ATRIAL FIBRILLATION1 reports
BAROTRAUMA1 reports
BLINDNESS TRANSIENT1 reports
BLOOD BILIRUBIN INCREASED1 reports
BLOOD CATECHOLAMINES INCREASED1 reports
BLOOD GASES ABNORMAL1 reports
BLOOD LACTATE DEHYDROGENASE INCREASED1 reports
BODY TEMPERATURE INCREASED1 reports
BONE PAIN1 reports
BRADYCARDIA FOETAL1 reports
BRAIN NATRIURETIC PEPTIDE INCREASED1 reports
BRAIN OEDEMA1 reports
BREAST ENLARGEMENT1 reports
BREATH SOUNDS ABNORMAL1 reports
C REACTIVE PROTEIN INCREASED1 reports
CARBON MONOXIDE POISONING1 reports
CARDIAC DYSFUNCTION1 reports
CARDIO RESPIRATORY ARREST1 reports
CARDIOMEGALY1 reports
CELLULITIS1 reports
CEREBELLAR INFARCTION1 reports
CEREBROVASCULAR ACCIDENT1 reports
CHEST DISCOMFORT1 reports

Report Outcomes

Out of 113 classified reports for CARBON DIOXIDE:

Serious 94.7%Non-Serious 5.3%

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

Female70 (66.7%)
Male33 (31.4%)
Unknown2 (1.9%)

Reports by Age

Age 437 reports
Age 675 reports
Age 554 reports
Age 734 reports
Age 764 reports
Age 373 reports
Age 523 reports
Age 583 reports
Age 593 reports
Age 633 reports
Age 703 reports
Age 723 reports
Age 743 reports
Age 803 reports
Age 32 reports
Age 262 reports
Age 302 reports
Age 422 reports
Age 452 reports
Age 502 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 CARBON DIOXIDE?

This profile reflects 267 FDA FAERS reports that mention CARBON DIOXIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CARBON DIOXIDE?

Frequently reported terms in FAERS include AIR EMBOLISM, SUBCUTANEOUS EMPHYSEMA, OFF LABEL USE, POST PROCEDURAL COMPLICATION, CARDIAC ARREST, HYPOTENSION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures CARBON DIOXIDE?

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