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Namenda Targets a Different Pathway
Glutamate-an important treatment target
- Glutamate plays an integral role in the neural pathways associated with learning and memory1
- Abnormal glutamate activity may cause neuronal dysfunction and cell death, leading to Alzheimer's disease symptoms1
The glutamate hypothesis of Alzheimer's disease1

Evidence suggests NAMENDA modulates abnormal glutamate activity2
There is no evidence that NAMENDA prevents or slows neurodegeneration in patients with Alzheimer's disease.2
A unique mechanism for treating Alzheimer's disease2
NAMENDAglutamate pathway
Preferred status on the majority of health plan and Medicare Part D formularies4
- A unique MOA puts NAMENDA in a class of its own, as categorized by USP Guidelines5
AChEIsacetylcholine pathway6
View a video animation of how the NAMENDA mechanism of action works
*NMDA=N-methyl-D-aspartate.
Under the Medicare Prescription Drug, Improvement, and Modernization Act (MMA), the United States Pharmacopeia (USP) developed Model Guidelines Version 2.0, outlining drug categories and classes that may be used by prescription drug plans in developing their formularies. The USP Guidelines were used as the classification structure for approximately 74% of formularies that were in place when the new Medicare Part D benefit became activated January 1, 2006.7,8
Important Safety Information
NAMENDA® (memantine HCl) is indicated for the treatment of moderate to severe Alzheimer's disease. NAMENDA has been used by more than 2 million people worldwide.NAMENDA is contraindicated in patients with known hypersensitivity to memantine HCl or any excipients used in the formulation. The most common adverse events reported with NAMENDA vs placebo (≥5% and higher than placebo) were dizziness, confusion, headache, and constipation. In patients with severe renal impairment, the dosage should be reduced.
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