975 reports of this reaction
2.5% of all ERYTHROPOIETIN reports
#7 most reported adverse reaction
NAUSEA is the #7 most commonly reported adverse reaction for ERYTHROPOIETIN, manufactured by Janssen Products, LP. There are 975 FDA adverse event reports linking ERYTHROPOIETIN to NAUSEA. This represents approximately 2.5% of all 39,177 adverse event reports for this drug.
Patients taking ERYTHROPOIETIN who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is a less commonly reported adverse event for ERYTHROPOIETIN, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for ERYTHROPOIETIN:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 975 FDA reports for ERYTHROPOIETIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 2.5% of all adverse event reports for ERYTHROPOIETIN, making it a notable side effect.
If you experience nausea while taking ERYTHROPOIETIN, 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.