695 reports of this reaction
1.5% of all PALIPERIDONE reports
#10 most reported adverse reaction
DYSTONIA is the #10 most commonly reported adverse reaction for PALIPERIDONE, manufactured by Janssen Pharmaceuticals, Inc.. There are 695 FDA adverse event reports linking PALIPERIDONE to DYSTONIA. This represents approximately 1.5% of all 45,344 adverse event reports for this drug.
Patients taking PALIPERIDONE who experience dystonia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSTONIA is a less commonly reported adverse event for PALIPERIDONE, but still significant enough to appear in the safety profile.
In addition to dystonia, the following adverse reactions have been reported for PALIPERIDONE:
The following drugs have also been linked to dystonia in FDA adverse event reports:
DYSTONIA has been reported as an adverse event in 695 FDA reports for PALIPERIDONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSTONIA accounts for approximately 1.5% of all adverse event reports for PALIPERIDONE, making it a notable side effect.
If you experience dystonia while taking PALIPERIDONE, 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.