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Figure 6 in the original guideline document provides the GRADE evidence profile.

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Seizures: Namenda has not been systematically evaluated in patients with a seizure disorder.

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Memantine DosageFor the treatment of moderate to severe dementia, Memantine is administered at 5 mg PO once daily initially.

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It main side effects are drowsiness and hypotension.

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There are no adequate and well-controlled trials documenting the safety and efficacy of memantine in any illness occurring in children.

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In addition, the neural correlates of improvement of language function can now be readily detectable with event-related potentials.

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Such behaviors are often the result of memory loss in the later stages of the disease.

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The effects could be a result of direct stimulation of brain-derived neurotrophic factor (BDNF) and its receptor.

Defeating Alzheimer's disease and other dementias: a priority for European science and society.

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Interestingly, memantine was shown to antagonize L812M-associated hyperactivity, and consistent with this result, memantine treatment of our proband resulted in the substantial reduction in his seizure burden.

Does the behavior affect only one resident and one staff member?

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Read this Patient Information that comes with memantine hydrochloride before you start taking it and each time you get a refill.

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Copyright 2016, Drug Information Service, University of Utah, Salt Lake City, UT.

Namenda side effects and adverse reactions include back pain and constipation.

These two forms of glutamate release cause a continual domino effect of excitotoxic cell death and further increased extracellular glutamate concentrations.

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