AIR

N/A

Manufactured by Strate Welding Supply Co., Inc.

87 FDA adverse event reports analyzed

Last updated: 2026-04-15

About AIR

AIR is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Strate Welding Supply Co., Inc.. The most commonly reported adverse reactions for AIR include CARDIAC ARREST, SINUS TACHYCARDIA, ATRIAL FIBRILLATION, BLOOD PRESSURE DECREASED, CYANOSIS. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for AIR.

Top Adverse Reactions

CARDIAC ARREST3 reports
SINUS TACHYCARDIA3 reports
ATRIAL FIBRILLATION2 reports
BLOOD PRESSURE DECREASED2 reports
CYANOSIS2 reports
DRUG INTERACTION2 reports
DYSTONIA2 reports
OXYGEN SATURATION DECREASED2 reports
POLYURIA2 reports
PRODUCT QUALITY ISSUE2 reports
UNDERDOSE2 reports
ACIDOSIS1 reports
ALANINE AMINOTRANSFERASE INCREASED1 reports
ANAESTHETIC COMPLICATION CARDIAC1 reports
ANAPHYLACTIC REACTION1 reports
ANEURYSM RUPTURED1 reports
ARRHYTHMIA1 reports
ASPARTATE AMINOTRANSFERASE INCREASED1 reports
BACK PAIN1 reports
BALANCE DISORDER1 reports
BLEEDING TIME PROLONGED1 reports
BLOOD CORTICOTROPHIN INCREASED1 reports
BLOOD CORTISOL INCREASED1 reports
BREATH SOUNDS ABSENT1 reports
CEREBROVASCULAR ACCIDENT1 reports
COMMUNICATION DISORDER1 reports
CONDITION AGGRAVATED1 reports
DEVICE CONNECTION ISSUE1 reports
DEVICE DAMAGE1 reports
DEVICE FAILURE1 reports
DEVICE ISSUE1 reports
DRUG INEFFECTIVE1 reports
DYSARTHRIA1 reports
DYSKINESIA1 reports
DYSPHAGIA1 reports
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION1 reports
HAEMORRHAGE1 reports
HEART RATE INCREASED1 reports
HEMIPARESIS1 reports
HYPERTENSION1 reports
HYPOKINESIA1 reports
HYPOTENSION1 reports
LOCAL SWELLING1 reports
LONG QT SYNDROME1 reports
MUSCLE SPASMS1 reports
MYOTONIA1 reports
NEPHROGENIC DIABETES INSIPIDUS1 reports
NO ADVERSE EVENT1 reports
OCULOGYRIC CRISIS1 reports
OFF LABEL USE1 reports
PAIN IN EXTREMITY1 reports
PCO2 INCREASED1 reports
PNEUMOTHORAX1 reports
POLLAKIURIA1 reports
POSTURE ABNORMAL1 reports
PROCEDURAL COMPLICATION1 reports
PROCEDURAL HAEMORRHAGE1 reports
PRODUCT PACKAGING QUANTITY ISSUE1 reports
PRODUCT USE IN UNAPPROVED INDICATION1 reports
PRODUCT USE ISSUE1 reports
PULMONARY EMBOLISM1 reports
PYREXIA1 reports
SUBCUTANEOUS EMPHYSEMA1 reports
SWELLING FACE1 reports
TACHYCARDIA1 reports
THIRST1 reports
TORSADE DE POINTES1 reports
TORTICOLLIS1 reports
VENOUS THROMBOSIS1 reports
VENTRICULAR EXTRASYSTOLES1 reports
VENTRICULAR TACHYCARDIA1 reports
VISUAL ACUITY REDUCED1 reports
VISUAL IMPAIRMENT1 reports
WRONG DRUG ADMINISTERED1 reports

Report Outcomes

Out of 20 classified reports for AIR:

Serious 90.0%Non-Serious 10.0%

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

Demographics Breakdown

Reports by Sex

Female13 (72.2%)
Male5 (27.8%)

Reports by Age

Age 592 reports
Age 692 reports
Age 141 reports
Age 161 reports
Age 361 reports
Age 481 reports
Age 521 reports
Age 551 reports
Age 581 reports
Age 721 reports
Age 771 reports
Age 831 reports
Age 851 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 AIR?

This profile reflects 87 FDA FAERS reports that mention AIR. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for AIR?

Frequently reported terms in FAERS include CARDIAC ARREST, SINUS TACHYCARDIA, ATRIAL FIBRILLATION, BLOOD PRESSURE DECREASED, CYANOSIS, DRUG INTERACTION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures AIR?

Labeling and FAERS entries often list Strate Welding Supply Co., Inc. in connection with AIR. 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.