Also known as: Tardive dyskinesia treatments, Huntington's disease medications
Medications for involuntary movement disorders (tardive dyskinesia, Huntington's disease chorea) work by depleting dopamine at nerve terminals. Several are metabolized by CYP2D6, which means poor metabolizers are at higher risk of dose-related side effects including sedation, depression, and QT prolongation. The FDA labels for valbenazine and deutetrabenazine include specific dose adjustments for CYP2D6 poor metabolizers.
Each link goes to the drug's full pharmacogenetics page with CPIC and FDA phenotype recommendations.
Combined products and brand names for the medications above. Each links to a pharmacogenetic breakdown.
This page covers the pharmacogenetics of movement disorder medications in general. A Gene2Rx report tells you how your personal genotype interacts with every drug on this page.
Get your report Look up a medicationInformational only, not medical advice. Pharmacogenetic guidelines describe population-level patterns that inform prescribing decisions. Never start, stop, or change a medication without talking to your prescribing clinician.