Now there’s more to the story. Now there’s B.E.N.
CSL Behring announced the launch of B.E.N. (Berinert Expert Network), a full-service support program for healthcare providers and for hereditary angioedema (HAE) patients and their caregivers. Learn more at http://www.berinert.com/
B.E.N. provides information and assistance designed to help healthcare providers and patients, including:
1. Securing access to Berinert – B.E.N. will assist HAE patients in initiating Berinert therapy when and where it is needed by:
- Helping their providers develop treatment plans that are appropriate for the individual patient
- Connecting patients to a specialty pharmacy that has Berinert available
- Identifying the nearest hospital with access to Berinert
- Guaranteeing the availability of one year's supply of Berinert to the first 1,000 patients who opt in to the B.E.N. program
3. Educational resources and tools – B.E.N. will provide resources to help patients manage their Berinert therapy, including a journal, patient ID card and magnet with key phone numbers
4. Assurance and Assistance -- Serving the rare disease communities for years, the CSL Behring Assurance and Assistance Programs, working through B.E.N., will ensure that:
- Patients who experience a lapse in third-party, private health insurance can access Berinert
- Qualified patients who are uninsured, underinsured, or who cannot afford their prescribed therapy can obtain Berinert.
Until the approval of Berinert, patients with HAE in the U.S. did not have a safe and effective treatment option that rapidly relieved the symptoms of acute attacks in the face and abdomen. In clinical trials, the median time to onset of relief with Berinert was 48 minutes as compared to more than 4 hours with placebo.
HAE can be an isolating health condition, but B.E.N will help patients connect with medical experts who can provide much needed information about their condition, and details on Berinert.
In addition, through B.E.N., HAE patients will be able connect with other patients via the U.S. Hereditary Angioedema Association (HAEA). In this way, patients can benefit from additional valuable programs and resources designed for and by people with HAE.
For more information on B.E.N. 24 hours a day, seven days a week, call toll-free 1-877-BEN-4HAE (1-877-236-4423).
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