342 reports of this reaction
0.6% of all NYSTATIN reports
#72 most reported adverse reaction
HAEMOGLOBIN DECREASED is the #72 most commonly reported adverse reaction for NYSTATIN, manufactured by Padagis US LLC. There are 342 FDA adverse event reports linking NYSTATIN to HAEMOGLOBIN DECREASED. This represents approximately 0.6% of all 59,130 adverse event reports for this drug.
NYSTATIN has an overall safety score of 82 out of 100. Patients taking NYSTATIN who experience haemoglobin decreased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HAEMOGLOBIN DECREASED is a less commonly reported adverse event for NYSTATIN, but still significant enough to appear in the safety profile.
In addition to haemoglobin decreased, the following adverse reactions have been reported for NYSTATIN:
The following drugs have also been linked to haemoglobin decreased in FDA adverse event reports:
HAEMOGLOBIN DECREASED has been reported as an adverse event in 342 FDA reports for NYSTATIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
HAEMOGLOBIN DECREASED accounts for approximately 0.6% of all adverse event reports for NYSTATIN, making it a notable side effect.
If you experience haemoglobin decreased while taking NYSTATIN, 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.