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See safety info including boxed warning. The fda has approved austedo xr in four new tablet strengths for adults diagnosed with tardive dyskinesia and chorea associated with huntington’s disease, according to the manufacturer Austedo xr and austedo may cause parkinsonism in patients with huntington’s disease or tardive dyskinesia

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Parkinsonism has also been observed with other vmat2 inhibitors. See safety info and boxed warning. 2.1 dosing information the dose of austedo xr and austedo is determined individually for each patient based on reduction of chorea or tardive dyskinesia and tolerability

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Table 1 displays the recommended dosage and important administration instructions of austedo xr and austedo when first prescribed to patients who are not being switched from tetrabenazine (a related vmat2 inhibitor).

Austedo's drug class is a vmat2 inhibitor (vesicular monoamine transporter 2 inhibitor) What is tardive dyskinesia (td) and chorea associated with huntington’s disease In a cohort of 27 participants, up to 77% reported enhancements in daily activities such as speech and eating after three months of treatment. The most common adverse reactions for austedo (4% and greater than placebo) in controlled clinical studies in patients with tardive dyskinesia were nasopharyngitis and insomnia

Reduce involuntary movements with austedo xr® (deutetrabenazine) tablets treatment for td