278 reports of this reaction
1.7% of all AMISULPRIDE reports
#10 most reported adverse reaction
EXTRAPYRAMIDAL DISORDER is the #10 most commonly reported adverse reaction for AMISULPRIDE, manufactured by Acacia Pharma Ltd. There are 278 FDA adverse event reports linking AMISULPRIDE to EXTRAPYRAMIDAL DISORDER. This represents approximately 1.7% of all 16,736 adverse event reports for this drug.
Patients taking AMISULPRIDE who experience extrapyramidal disorder should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
EXTRAPYRAMIDAL DISORDER is a less commonly reported adverse event for AMISULPRIDE, but still significant enough to appear in the safety profile.
In addition to extrapyramidal disorder, the following adverse reactions have been reported for AMISULPRIDE:
The following drugs have also been linked to extrapyramidal disorder in FDA adverse event reports:
EXTRAPYRAMIDAL DISORDER has been reported as an adverse event in 278 FDA reports for AMISULPRIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
EXTRAPYRAMIDAL DISORDER accounts for approximately 1.7% of all adverse event reports for AMISULPRIDE, making it a notable side effect.
If you experience extrapyramidal disorder while taking AMISULPRIDE, 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.