VALBENAZINE and PARKINSONISM

598 reports of this reaction

1.7% of all VALBENAZINE reports

#16 most reported adverse reaction

Overview

PARKINSONISM is the #16 most commonly reported adverse reaction for VALBENAZINE, manufactured by Neurocrine Biosciences, Inc.. There are 598 FDA adverse event reports linking VALBENAZINE to PARKINSONISM. This represents approximately 1.7% of all 34,810 adverse event reports for this drug.

Patients taking VALBENAZINE who experience parkinsonism should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

PARKINSONISM598 of 34,810 reports

PARKINSONISM is a less commonly reported adverse event for VALBENAZINE, but still significant enough to appear in the safety profile.

Other Side Effects of VALBENAZINE

In addition to parkinsonism, the following adverse reactions have been reported for VALBENAZINE:

Other Drugs Associated with PARKINSONISM

The following drugs have also been linked to parkinsonism in FDA adverse event reports:

FLUPHENAZINE HYDROCHLORIDE

Frequently Asked Questions

Does VALBENAZINE cause PARKINSONISM?

PARKINSONISM has been reported as an adverse event in 598 FDA reports for VALBENAZINE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is PARKINSONISM with VALBENAZINE?

PARKINSONISM accounts for approximately 1.7% of all adverse event reports for VALBENAZINE, making it a notable side effect.

What should I do if I experience PARKINSONISM while taking VALBENAZINE?

If you experience parkinsonism while taking VALBENAZINE, 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.

Related Pages

VALBENAZINE Full ProfileAll Drugs Causing PARKINSONISMNeurocrine Biosciences, Inc. Drugs
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.