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Access & Support

Access

Help your patients get the medication they need

UCB is committed to making BRIVIACT accessible for the majority of eligible patients across the US

ABOUT

2OUT
OF
3

patients could have
access to BRIVIACT first

This means they should not have to try and fail
other antiseizure medications, including generics,
for their insurance to cover BRIVIACT.1*

9OUT
OF
10

commercial patients have
formulary access to BRIVIACT2

*

Formularies can change and many health plans offer more than one formulary. Please check directly with the health plan to confirm coverage for individual patients.1

Savings

BRIVIACT Patient Savings Program

BRIVIACT® patient savings card

Savings card is not valid for use by patients who are covered by any federally funded or state-funded healthcare program (including, but not limited to, Medicare [Part D and Medigap] and those who are Medicare eligible and enrolled in an employer-sponsored health plan for retirees, Medicaid, any state pharmaceutical assistance program, TRICARE, VA, or DoD), or for cash-paying patients. A valid BRIVIACT prescription consistent with the approved FDA labeling is required. Other eligibility criteria and terms apply. Full eligibility criteria and terms are available at www.BRIVIACT.com or upon request by calling UCBCares® at 833-948-2394.

Enhanced copay support for eligible commercial
BRIVIACT patients

UCB has expanded out-of-pocket support for BRIVIACT to help patients afford their medication

UCB is introducing enhancements to the BRIVIACT prescription savings program for eligible commercial patients

Affordable payments

Most commercially insured patients should pay as little as $10 for their BRIVIACT prescription. No copay card will be required when filling a prescription at a participating pharmacy.

Additional support with the eVoucher

Beginning in January 2024, more than 90% of retail pharmacies across the US will participate in the eVoucher savings program so eligible commercial patients will automatically receive out-of-pocket support at the point of adjudication.

Increased out-of-pocket support starting in 2024

UCB is increasing the maximum patient savings to $1,500 per script and $6,000 per year. Support will be available at participating pharmacies for eligible commercially insured patients.

The eVoucher savings program is not for use by patients who are covered by any federally funded or state-funded healthcare program (including, but not limited to, Medicare [Part D and Medigap] and those who are Medicare eligible and enrolled in an employer-sponsored health plan for retirees, Medicaid, any state pharmaceutical assistance program, TRICARE, VA, or DoD), or for cash-paying patients. Offer good only in the US, including Puerto Rico.

 

The eVoucher savings program may only be used with a valid BRIVIACT prescription consistent with the approved FDA labeling at the time the prescription is filled by the pharmacist and dispensed to the patient. The maximum annual benefit amount is $6,000 per calendar year. Void where prohibited by law, taxed, or restricted. This offer cannot be combined with any other promotional offer. UCB, Inc. reserves the right to rescind, revoke, or amend this offer without notice at any time. No cash value. Not eligible for sale, purchase, trade, or counterfeit.

Assistance

Helping eligible patients start on BRIVIACT

New patients may be eligible for a FREE trial voucher with a 14-day prescription

BRIVIACT® 14-day voucher

The BRIVIACT Patient Assistance Program may be able to help if your patients do not have health insurance or otherwise cannot afford BRIVIACT.

To learn more about the BRIVIACT Patient Assistance Program and check eligibility:

Get helpful resources
for patients, caregivers,
and practices

References: 1. Managed Markets Insight & Technology, LLC, database as of August 2021. 2. Data on file. UCB, Inc.

Indication

BRIVIACT® (brivaracetam) CV is indicated for the treatment of partial-onset seizures in patients 1 month of age and older.

Important Safety Information

WARNINGS AND PRECAUTIONS

  • Suicidal Behavior and Ideation: Antiepileptic drugs, including BRIVIACT, increase the risk of suicidal behavior and ideation. Monitor patients taking BRIVIACT for the emergence or worsening of depression; unusual changes in mood or behavior; or suicidal thoughts, behavior, or self-harm. Advise patients, their caregivers, and/or families to be alert for these behavioral changes and report them immediately to a healthcare provider.
  • Neurological Adverse Reactions: BRIVIACT causes somnolence, fatigue, dizziness, and disturbance in coordination. Somnolence and fatigue-related adverse reactions were reported in 25% of adult patients taking at least 50 mg per day of BRIVIACT compared to 14% of adult patients taking placebo. Dizziness and disturbance in gait and coordination were reported in 16% of adult patients taking at least 50 mg per day of BRIVIACT compared to 10% of adult patients taking placebo. The risk is greatest early in treatment but can occur at any time. Monitor patients for these signs and symptoms and advise them not to drive or operate machinery until they have gained sufficient experience on BRIVIACT.
  • Psychiatric Adverse Reactions: BRIVIACT causes psychiatric adverse reactions, including non-psychotic and psychotic symptoms. These events were reported in approximately 13% of adult patients taking at least 50 mg per day of BRIVIACT compared to 8% of adult patients taking placebo. A total of 1.7% of adult patients taking BRIVIACT discontinued treatment due to psychiatric reactions compared to 1.3% of patients taking placebo. Psychiatric adverse reactions were also observed in open-label pediatric trials and were generally similar to those observed in adults. Advise patients to report these symptoms immediately to a healthcare provider.
  • Hypersensitivity: BRIVIACT can cause hypersensitivity reactions. Bronchospasm and angioedema have been reported. Discontinue BRIVIACT if a patient develops a hypersensitivity reaction after treatment. BRIVIACT is contraindicated in patients with a prior hypersensitivity reaction to brivaracetam or any of the inactive ingredients.
  • Withdrawal of Antiepileptic Drugs: As with all antiepileptic drugs, BRIVIACT should generally be withdrawn gradually because of the risk of increased seizure frequency and status epilepticus.

DOSING CONSIDERATIONS

  • Dose adjustments are recommended for patients with all stages of hepatic impairment.
  • When BRIVIACT is co-administered with rifampin, an increase in the BRIVIACT dose is recommended.

ADVERSE REACTIONS

In adult adjunctive therapy placebo-controlled clinical trials, the most common adverse reactions (at least 5% for BRIVIACT and at least 2% more frequently than placebo) were somnolence and sedation, dizziness, fatigue, and nausea and vomiting symptoms. Adverse reactions reported in clinical studies of pediatric patients were generally similar to those in adult patients. Adverse reactions with BRIVIACT injection in adult and pediatric patients were generally similar to those observed with BRIVIACT tablets. Other adverse events that occurred in adult patients who received BRIVIACT injection included dysgeusia, euphoric mood, feeling drunk, and infusion site pain.

BRIVIACT is a Schedule V controlled substance.

Please see full Prescribing Information.