Shared Solutions provides support for you and your patients to help achieve treatment goals

Support for your office: Shared Solutions streamlines access and works directly with your preferred pharmacy to fill prescriptions to help get patients started*

Support for your patients: Shared Solutions provides support with access, affordability, and adherence—including nurse support and patient education¹

Two ways to get started with Shared Solutions

Enroll your patient:

Complete the PSRF and obtain your patient’s signature to receive full benefits from Shared Solutions. Fax completed form to 1-844-257-6126.

Patient self-enrollment:

Patients can self-enroll for nurse support and financial assistance at any time by visiting MySharedSolutions.com.

Utilize iAssist to enroll your patients (if available at your office).

Shared Solutions provides ongoing patient support by covering the “3 A’s”:

ACCESS—Shared Solutions helps by managing:

Prior authorization and appeals
Pharmacy identification and referral
Insurance benefits, Medicare Part D, and Medicaid verification and navigation

AFFORDABILITY—Shared Solutions determines the appropriate financial assistance offerings for your patients

Free Trial Vouchers are available to new patients for 4 weeks of titration or 30 days of maintenance^†
Copay Cards are available to eligible, commercially insured patients—they may pay as little as $0 on each fill^†

ADHERENCE—Shared Solutions supports patients in reaching their goals with¹:

Proactive nurse communication (phone, SMS, email, direct mail)
Adherence support, expectation reinforcement, dosing and titration guidance
Patient education
Tools and resources to help manage their treatment

Shared Solutions is available Monday-Friday from 8 AM to 8 PM CT

To reach the dedicated line for HD chorea: Call 1-800-887-8100, Option #2 for AUSTEDO, then Option #6
Your patients can also visit
MySharedSolutions.com at any time

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

^‡If you don’t have a Patient Support Specialist, reach out to your sales representative.

Find information on cost & coverage

*Fill out preferred pharmacy on PSRF. Shared Solutions will route to HCP or patient-preferred pharmacies if in network.

^†See Terms and Conditions on www.AUSTEDOcardform.com.

HD, Huntington’s disease; PSRF, Prescription and Service Request Form.

REFERENCE: 1. Data on file. Parsippany, NJ: Teva Neuroscience, Inc.

Important safety information

Depression and Suicidality in Patients with Huntington’s Disease: 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 is contraindicated in patients who are suicidal, and in patients with untreated or inadequately treated depression.

Contraindications: AUSTEDO is contraindicated in patients with Huntington’s disease who are suicidal, or have untreated or inadequately treated depression. AUSTEDO is 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 (Xenazine^®) or valbenazine (Ingrezza^®).

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

QTc Prolongation: AUSTEDO may prolong the QT interval, but the degree of QT prolongation is not clinically significant when AUSTEDO is administered within the recommended dosage range. 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; intensive symptomatic treatment and medical monitoring; and treatment of any concomitant serious medical problems.

Akathisia, Agitation, and Restlessness: 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 dose should be reduced; some patients may require discontinuation of therapy.

Parkinsonism: 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 dose should be reduced; some patients may require discontinuation of therapy.

Sedation and Somnolence: Sedation is a common dose-limiting adverse reaction of 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 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.

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.

Please see full Prescribing Information, including Boxed Warning.

The brands listed are registered trademarks of their respective owners.