Support & Getting Started

Cost & Coverage Support

~90% of patients pay $10 or less with financial assistance offerings¹

New, non-sampled patients can receive
their first
30 days of AUSTEDO XR for free.

Voucher available at
AUSTEDOcardform.com.

Remind pharmacy to apply.

Terms & Conditions apply

Patients may pay as little as $0 per
month for AUSTEDO XR.

Patients must self-enroll at
MySharedSolutions.com.

Visit AUSTEDOcardform.com to send a
link
to patients with more information.

Terms & Conditions apply

Patients who qualify for and utilize LIS
may pay as little as $10.35 per month.²

Shared Solutions can help patients understand if they qualify. To enroll in Shared Solutions, patients can visit MySharedSolutions.com.

To qualify, patient must:

Apply for assistance
Be a legal US resident
Meet the insurance
eligibility criteria
Be below the income
eligibility limit

To apply, patient must complete the application on MySharedSolutions.com.

~88% of AUSTEDO prescriptions are successfully processed and approved¹

Access for 94% of patients with insurance coverage (commercial, Medicare Part D, and Medicaid)¹
Available at both specialty and retail pharmacies

Request a visit from a Patient Support Specialist who can help with access and reimbursement, prescription pull-through, and patient assistance support*

*If you do not have a Patient Support Specialist, reach out to your sales representative.

Prescription
coverage tool

Find health plans that cover AUSTEDO^® XR (deutetrabenazine) extended-release tablets in your state

Enter in a ZIP code or select a state, then select a plan type, select a plan, and click “Search.”

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NA, not available.
Please note that plans may have multiple formularies and they are subject to change by the plan. Please check with the health plan directly to confirm formulary status, requirements, and coverage information for individual patients.
Source: Fingertip Formulary database as of 10/2023.
This information is intended only to show the formulary coverage status for each product and should not be construed to make any comparisons of safety, efficacy, or other clinical outcome.

VIEW RESOURCES FOR
YOU & YOUR PATIENTS

REFERENCES: 1. Data on file. Parsippany, NJ: Teva Neuroscience, Inc. 2. Medicare. Find your level of Extra Help (Part D). Accessed January 9, 2023. https://www.medicare.gov/your-medicare-costs/get-help-paying-costs/find-your-level-of-extra-help-part-d

Important safety information

Depression and Suicidality in Patients with Huntington’s Disease: AUSTEDO XR and AUSTEDO can increase the risk of depression and suicidal thoughts and behavior (suicidality) in patients with Huntington’s disease. Balance the risks of depression and suicidality with the clinical need for treatment of chorea. Closely monitor patients for the emergence or worsening of depression, suicidality, or unusual changes in behavior. Inform patients, their caregivers, and families of the risk of depression and suicidality and instruct them to report behaviors of concern promptly to the treating physician. Exercise caution when treating patients with a history of depression or prior suicide attempts or ideation. AUSTEDO XR and AUSTEDO are contraindicated in patients who are suicidal, and in patients with untreated or inadequately treated depression.

Contraindications: AUSTEDO XR and AUSTEDO are contraindicated in patients with Huntington’s disease who are suicidal, or have untreated or inadequately treated depression. AUSTEDO XR and AUSTEDO are also contraindicated in: patients with hepatic impairment; patients taking reserpine or within 20 days of discontinuing reserpine; patients taking monoamine oxidase inhibitors (MAOIs), or within 14 days of discontinuing MAOI therapy; and patients taking tetrabenazine or valbenazine.

Clinical Worsening and Adverse Events in Patients with Huntington’s Disease: AUSTEDO XR and AUSTEDO may cause a worsening in mood, cognition, rigidity, and functional capacity. Prescribers should periodically re-evaluate the need for AUSTEDO XR or AUSTEDO in their patients by assessing the effect on chorea and possible adverse effects.

QTc Prolongation: AUSTEDO XR and AUSTEDO may prolong the QT interval, but the degree of QT prolongation is not clinically significant when AUSTEDO XR or AUSTEDO is administered within the recommended dosage range. AUSTEDO XR and AUSTEDO should be avoided in patients with congenital long QT syndrome and in patients with a history of cardiac arrhythmias.

Neuroleptic Malignant Syndrome (NMS), a potentially fatal symptom complex reported in association with drugs that reduce dopaminergic transmission, has been observed in patients receiving tetrabenazine. The risk may be increased by concomitant use of dopamine antagonists or antipsychotics. The management of NMS should include immediate discontinuation of AUSTEDO XR and AUSTEDO; intensive symptomatic treatment and medical monitoring; and treatment of any concomitant serious medical problems.

Akathisia, Agitation, and Restlessness: AUSTEDO XR and AUSTEDO may increase the risk of akathisia, agitation, and restlessness. The risk of akathisia may be increased by concomitant use of dopamine antagonists or antipsychotics. If a patient develops akathisia, the AUSTEDO XR or AUSTEDO dose should be reduced; some patients may require discontinuation of therapy.

Parkinsonism: AUSTEDO XR and AUSTEDO may cause parkinsonism in patients with Huntington’s disease or tardive dyskinesia. Parkinsonism has also been observed with other VMAT2 inhibitors. The risk of parkinsonism may be increased by concomitant use of dopamine antagonists or antipsychotics. If a patient develops parkinsonism, the AUSTEDO XR or AUSTEDO dose should be reduced; some patients may require discontinuation of therapy.

Sedation and Somnolence: Sedation is a common dose-limiting adverse reaction of AUSTEDO XR and AUSTEDO. Patients should not perform activities requiring mental alertness, such as operating a motor vehicle or hazardous machinery, until they are on a maintenance dose of AUSTEDO XR or AUSTEDO and know how the drug affects them. Concomitant use of alcohol or other sedating drugs may have additive effects and worsen sedation and somnolence.

Hyperprolactinemia: Tetrabenazine elevates serum prolactin concentrations in humans. If there is a clinical suspicion of symptomatic hyperprolactinemia, appropriate laboratory testing should be done and consideration should be given to discontinuation of AUSTEDO XR and AUSTEDO.

Binding to Melanin-Containing Tissues: Deutetrabenazine or its metabolites bind to melanin-containing tissues and could accumulate in these tissues over time. Prescribers should be aware of the possibility of long-term ophthalmologic effects.

Common Adverse Reactions: The most common adverse reactions for AUSTEDO (>8% and greater than placebo) in a controlled clinical study in patients with Huntington’s disease were somnolence, diarrhea, dry mouth, and fatigue. 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. Adverse reactions with AUSTEDO XR extended-release tablets are expected to be similar to AUSTEDO tablets.

Please see full Prescribing Information, including Boxed Warning.

~90% of patients pay $10 or less with financial assistance offerings1

~88% of AUSTEDO prescriptions are successfully processed and approved1

Prescription coverage tool

Find health plans that cover AUSTEDO® XR (deutetrabenazine) extended-release tablets in your state

Find health plans that cover AUSTEDO® XR (deutetrabenazine) extended-release tablets in your state

~90% of patients pay $10 or less with financial assistance offerings¹

~88% of AUSTEDO prescriptions are successfully processed and approved¹

Prescription
coverage tool

Find health plans that cover AUSTEDO^® XR (deutetrabenazine) extended-release tablets in your state

Find health plans that cover AUSTEDO^® XR (deutetrabenazine) extended-release tablets in your state