33 reports of this reaction
2.4% of all SODIUM NITROPRUSSIDE reports
#15 most reported adverse reaction
MULTI ORGAN FAILURE is the #15 most commonly reported adverse reaction for SODIUM NITROPRUSSIDE, manufactured by EXELA PHARMA SCIENCES, LLC. There are 33 FDA adverse event reports linking SODIUM NITROPRUSSIDE to MULTI ORGAN FAILURE. This represents approximately 2.4% of all 1,403 adverse event reports for this drug.
Patients taking SODIUM NITROPRUSSIDE who experience multi organ failure should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MULTI ORGAN FAILURE is a less commonly reported adverse event for SODIUM NITROPRUSSIDE, but still significant enough to appear in the safety profile.
In addition to multi organ failure, the following adverse reactions have been reported for SODIUM NITROPRUSSIDE:
The following drugs have also been linked to multi organ failure in FDA adverse event reports:
MULTI ORGAN FAILURE has been reported as an adverse event in 33 FDA reports for SODIUM NITROPRUSSIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
MULTI ORGAN FAILURE accounts for approximately 2.4% of all adverse event reports for SODIUM NITROPRUSSIDE, making it a notable side effect.
If you experience multi organ failure while taking SODIUM NITROPRUSSIDE, 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.