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See prescribing information, including boxed warning Eric hughes, executive vice president of global r&d at teva, the study aims to enhance understanding of td's comprehensive impact and the effectiveness of available treatments. Review results from the pivotal studies for austedo.
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 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. See important safety information, including boxed warning
Learn about the results of the clinical studies done for austedo xr® (deutetrabenazine) tablets.
The data presented at a significant neuroscience congress demonstrate the effectiveness of austedo and austedo xr in reducing the severity of involuntary movements and enhancing quality of life for patients with tardive dyskinesia. Austedo xr and austedo are the first vesicular monoamine transporter 2 (vmat2) inhibitors approved by the u.s Food and drug administration in adults for the treatment of tardive dyskinesia and for the treatment of chorea associated with huntington’s disease Safety and effectiveness in pediatric patients have not been established.
In this interim analysis of data from 131 respondents, results revealed that 87% reported satisfaction with the medication overall, and 74% reported that their extra movements improved with austedo xr.
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