NITROGEN

N/A

Manufactured by AIRGAS USA, LLC

239 FDA adverse event reports analyzed

Last updated: 2026-04-15

About NITROGEN

NITROGEN is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by AIRGAS USA, LLC. The most commonly reported adverse reactions for NITROGEN include MALAISE, OFF LABEL USE, DRUG INTERACTION, ACCIDENTAL EXPOSURE TO PRODUCT, COMPLETED SUICIDE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for NITROGEN.

Top Adverse Reactions

MALAISE10 reports
OFF LABEL USE9 reports
DRUG INTERACTION7 reports
ACCIDENTAL EXPOSURE TO PRODUCT6 reports
COMPLETED SUICIDE5 reports
DYSPNOEA5 reports
NAUSEA5 reports
PRODUCT LEAKAGE5 reports
PSORIASIS5 reports
DEATH4 reports
DRY GANGRENE4 reports
EXTREMITY NECROSIS4 reports
HAEMODYNAMIC INSTABILITY4 reports
INJECTION SITE REACTION4 reports
PRODUCT USE IN UNAPPROVED INDICATION4 reports
PRODUCT USE ISSUE4 reports
VENTRICULAR FIBRILLATION4 reports
WEIGHT DECREASED4 reports
AIR EMBOLISM3 reports
ASTHENIA3 reports
DISEASE PROGRESSION3 reports
DIZZINESS3 reports
DRUG ADMINISTRATION ERROR3 reports
DRUG DEPENDENCE3 reports
FEELING ABNORMAL3 reports
PAIN3 reports
PAIN IN EXTREMITY3 reports
SQUAMOUS CELL CARCINOMA3 reports
TREMOR3 reports
ACCIDENTAL OVERDOSE2 reports
ADENOCARCINOMA OF COLON2 reports
ADVERSE EVENT2 reports
ANGINA PECTORIS2 reports
APPLICATION SITE ERYTHEMA2 reports
APPLICATION SITE VESICLES2 reports
BACK PAIN2 reports
BLOOD CHOLESTEROL INCREASED2 reports
CARDIAC ARREST2 reports
CARDIO RESPIRATORY ARREST2 reports
CATARACT2 reports
CEREBROVASCULAR ACCIDENT2 reports
CHILLS2 reports
DEHYDRATION2 reports
DRUG ABUSE2 reports
DYSGEUSIA2 reports
EYE IRRITATION2 reports
FALL2 reports
GAIT DISTURBANCE2 reports
HEPATITIS2 reports
HYPERTENSION2 reports
HYPOXIA2 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION2 reports
INCORRECT DRUG ADMINISTRATION DURATION2 reports
INSOMNIA2 reports
INTENTIONAL PRODUCT MISUSE2 reports
LIVER DISORDER2 reports
MELANOCYTIC NAEVUS2 reports
MENTAL STATUS CHANGES2 reports
MYOCARDIAL INFARCTION2 reports
NERVE COMPRESSION2 reports
PERIPHERAL SWELLING2 reports
PNEUMONIA2 reports
PNEUMOTHORAX2 reports
PRODUCT ODOUR ABNORMAL2 reports
RASH2 reports
SQUAMOUS CELL CARCINOMA OF SKIN2 reports
SUBCUTANEOUS EMPHYSEMA2 reports
SUBSTANCE USE2 reports
SWELLING FACE2 reports
UNRESPONSIVE TO STIMULI2 reports
VISION BLURRED2 reports
ABDOMINAL DISCOMFORT1 reports
ABDOMINAL PAIN1 reports
ACTINIC KERATOSIS1 reports
AGITATION1 reports
AIRWAY BURNS1 reports
ALKALOSIS1 reports
AMAUROSIS FUGAX1 reports
ANURIA1 reports
ANXIETY1 reports
AORTIC VALVE INCOMPETENCE1 reports
APPLICATION SITE DRYNESS1 reports
APPLICATION SITE EXFOLIATION1 reports
APPLICATION SITE FISSURE1 reports
APPLICATION SITE HAEMORRHAGE1 reports
APPLICATION SITE PAIN1 reports
APPLICATION SITE PRURITUS1 reports
APPLICATION SITE RASH1 reports
APPLICATION SITE REACTION1 reports
APPLICATION SITE SWELLING1 reports
APPLICATION SITE WARMTH1 reports
ARTHRALGIA1 reports
ARTHRITIS INFECTIVE1 reports
ASPHYXIA1 reports
BACK DISORDER1 reports
BACK INJURY1 reports
BALANCE DISORDER1 reports
BASAL CELL CARCINOMA1 reports
BLISTER1 reports
BLOOD ALKALINE PHOSPHATASE INCREASED1 reports

Report Outcomes

Out of 101 classified reports for NITROGEN:

Serious 85.1%Non-Serious 14.9%

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

Male45 (53.6%)
Female39 (46.4%)

Reports by Age

Age 427 reports
Age 73 reports
Age 323 reports
Age 703 reports
Age 793 reports
Age 42 reports
Age 232 reports
Age 242 reports
Age 252 reports
Age 342 reports
Age 622 reports
Age 692 reports
Age 782 reports
Age 812 reports
Age 822 reports
Age 01 reports
Age 21 reports
Age 61 reports
Age 121 reports
Age 131 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 NITROGEN?

This profile reflects 239 FDA FAERS reports that mention NITROGEN. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for NITROGEN?

Frequently reported terms in FAERS include MALAISE, OFF LABEL USE, DRUG INTERACTION, ACCIDENTAL EXPOSURE TO PRODUCT, COMPLETED SUICIDE, DYSPNOEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures NITROGEN?

Labeling and FAERS entries often list AIRGAS USA, LLC in connection with NITROGEN. 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.