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Special points of interest th December 24 2014 FDA approved the release of Namzaric Used for the treatment of: Moderate to severe dementia of the Alzheimer's type in patients stabilized on memantine hydrochloride and donepezil hydrochloride. Dosage: Once daily oral capsule. Marketing Information from Manufacturer: "Namzaric (nam-ZAIR-ick) combines, in one capsule, two complementary therapeutic agents which are often co-prescribed as approximately 70% of Namenda XR patients. Both Namenda XR and donepezil have proven efficacy and safety, for the treatment of moderate to severe Alzheimer's disease. Additionally, data has shown that combination therapy demonstrated greater improvement in cognition and global function verses one of the drugs alone," said David Nicholson, Actavis Senior Vice President, Global Brands R&D. Benefits and Concerns of the Drug: For patients who are stabilized on these two complimentary therapeutic agents, Namzaric offers and predictable dosing in an easy to use dosage form. But, fixed dosage forms generally limit the ability to tailor the patient dosing of each ingredient around their specific needs. And, patients that may take more medication than required may over dose which is problematic with extended release capsules. Both of these concerns are real concerns with Alzheimer’s patients. Coverage Recommendations: These recommendations are available to IPC/EvergreenRx clients from their Account Manager or Clinical Pharmacist. Please contact us with any questions or comments B r an d Na m e Nam z ar ic (n am -Z AIR - ic k ) Nam z ar ic , f or m er l y kn own as M D X -8 70 4 , is a on ce -d a il y or a l cap su le Gen er ic n am e d on ep ez i l & m em an ti n e T 636.614.1344 www.ipc-inc.com A Brown & Brown company