4 reports of this reaction
1.7% of all NITROGEN reports
#17 most reported adverse reaction
VENTRICULAR FIBRILLATION is the #17 most commonly reported adverse reaction for NITROGEN, manufactured by AIRGAS USA, LLC. There are 4 FDA adverse event reports linking NITROGEN to VENTRICULAR FIBRILLATION. This represents approximately 1.7% of all 239 adverse event reports for this drug.
Patients taking NITROGEN who experience ventricular fibrillation should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
VENTRICULAR FIBRILLATION is a less commonly reported adverse event for NITROGEN, but still significant enough to appear in the safety profile.
In addition to ventricular fibrillation, the following adverse reactions have been reported for NITROGEN:
The following drugs have also been linked to ventricular fibrillation in FDA adverse event reports:
VENTRICULAR FIBRILLATION has been reported as an adverse event in 4 FDA reports for NITROGEN. This does not prove causation, but indicates an association observed in post-market surveillance data.
VENTRICULAR FIBRILLATION accounts for approximately 1.7% of all adverse event reports for NITROGEN, making it a notable side effect.
If you experience ventricular fibrillation while taking NITROGEN, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.