Access & Support

Access & Affordability

Patient access & affordability with AUSTEDO XR

Preferred coverage¹

AUSTEDO XR has preferred coverage across a majority of national Medicare Part D plans.

Find Local Coverage

~90% of patients pay $10 or less¹

Patients can start AUSTEDO XR for $0 with 30-day Free Trial Voucher. Additional financial assistance support available for eligible patients.*

Financial Assistance Offerings

Comprehensive support to get patients started

Services available through CoverMyMeds:

Initiate, submit, and monitor PA requests in one central hub when prescribing
Option to enroll patients in Shared Solutions directly from CoverMyMeds portal for:
- Benefits investigation
- Affordability assistance
- Ongoing patient support, including nurse calls (patient authorization required)

To get started with CoverMyMeds: Log into an existing account at CoverMyMeds.com, or create one for free.

Shared Solutions can help with:

Access

Navigating patients’ insurance:

Conducting benefits verification
Identifying in-network pharmacies
Support throughout the Prior Authorization process

Affordability

Identifying financial assistance offerings:

Free Trial Voucher
Copay Card

Adherence¹

Ongoing treatment support from a dedicated nurse:

Adherence support
Expectation reinforcement
Dosing and titration guidance
Patient education
Tools and resources to help manage treatment

Patient enrollment in Shared Solutions:

You can enroll patients starting on AUSTEDO XR via the CoverMyMeds portal or by using the Prescription Service Request Form (patient authorization required)
Patients can also self-enroll at MySharedSolutions.com (also accessible from QR code on 4-week Titration Kit)

ARMs can assist with:

Education about PA process (including CoverMyMeds portal)
Information on affordability programs, payer coverage, and reimbursement
Education on the Shared Solutions and other patient support

Request a visit from an ARM or ask your Teva Sales Representative to connect you with your local ARM for more information.

Teva Shared Solutions^® can help patients understand financial assistance options available to them.

*Certain restrictions apply. Terms and conditions on AUSTEDOcardform.com.

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

Getting started at no cost (30 days)

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

Continuing treatment after first 30 days

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
pay no more than $11.20 per month.²

For patients who are uninsured or unable to afford AUSTEDO XR/AUSTEDO, the Teva Cares Foundation may be able to help.

Teva Cares is an independent, non-profit program that provides AUSTEDO XR/AUSTEDO at no cost to eligible patients.^†

To learn more, visit TevaCares.org or call 1-877-237-4881.

^†Patient must reside in the United States, meet insurance and income requirements, and have a valid prescription.

89% 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

Prescription
coverage tool

Find health plans that cover AUSTEDO XR extended-release tablets in your state

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

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N/A, 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 11/2024.
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

CoverMyMeds is a registered trademark of CoverMyMeds LLC.

REFERENCES: 1. Data on file. Parsippany, NJ: Teva Neuroscience, Inc. 2. Medicare. Find your level of Extra Help (Part D). Accessed May 7, 2024. https://www.medicare.gov/basics/costs/help/drug-costs

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.

Patient access & affordability with AUSTEDO XR

Preferred coverage1

~90% of patients pay $10 or less1

Comprehensive support to get patients started

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

89% of AUSTEDO prescriptions are successfully processed and approved1

Prescription coverage tool

Find health plans that cover AUSTEDO XR extended-release tablets in your state

Find health plans that cover AUSTEDO XR extended-release tablets in your state

Preferred coverage¹

~90% of patients pay $10 or less¹

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

89% of AUSTEDO prescriptions are successfully processed and approved¹

Prescription
coverage tool