223 reports of this reaction
2.7% of all SAPROPTERIN DIHYDROCHLORIDE reports
#7 most reported adverse reaction
NAUSEA is the #7 most commonly reported adverse reaction for SAPROPTERIN DIHYDROCHLORIDE, manufactured by BioMarin Pharmaceutical Inc.. There are 223 FDA adverse event reports linking SAPROPTERIN DIHYDROCHLORIDE to NAUSEA. This represents approximately 2.7% of all 8,360 adverse event reports for this drug.
Patients taking SAPROPTERIN DIHYDROCHLORIDE 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 SAPROPTERIN DIHYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for SAPROPTERIN DIHYDROCHLORIDE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 223 FDA reports for SAPROPTERIN DIHYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 2.7% of all adverse event reports for SAPROPTERIN DIHYDROCHLORIDE, making it a notable side effect.
If you experience nausea while taking SAPROPTERIN DIHYDROCHLORIDE, 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.