42 reports of this reaction
3.0% of all SODIUM NITROPRUSSIDE reports
#10 most reported adverse reaction
ANHEDONIA is the #10 most commonly reported adverse reaction for SODIUM NITROPRUSSIDE, manufactured by EXELA PHARMA SCIENCES, LLC. There are 42 FDA adverse event reports linking SODIUM NITROPRUSSIDE to ANHEDONIA. This represents approximately 3.0% of all 1,403 adverse event reports for this drug.
Patients taking SODIUM NITROPRUSSIDE who experience anhedonia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ANHEDONIA is a less commonly reported adverse event for SODIUM NITROPRUSSIDE, but still significant enough to appear in the safety profile.
In addition to anhedonia, the following adverse reactions have been reported for SODIUM NITROPRUSSIDE:
The following drugs have also been linked to anhedonia in FDA adverse event reports:
ANHEDONIA has been reported as an adverse event in 42 FDA reports for SODIUM NITROPRUSSIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ANHEDONIA accounts for approximately 3.0% of all adverse event reports for SODIUM NITROPRUSSIDE, making it a notable side effect.
If you experience anhedonia 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.