Abstract
In the EU, once-daily memantine 20 mg (Axura®, Ebixa®) is an option for the management of patients with moderate to severe Alzheimer’s disease (AD). In pooled clinical trials and studies in the clinical practice setting, memantine 20 mg/day improved cognition, functional ability and behavioural symptoms in this patient population. The beneficial effects of memantine are associated with delays in the need for full-time care, which were predicted to result in cost savings relative to standard care in recent cost-utility analyses in patients with moderate to severe AD conducted in EU countries. Memantine is well tolerated, with an adverse event profile that is similar to that with placebo.
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Disclosure
This article was updated from CNS Drugs 2009; 23 (10): 881-97 [39]. The preparation of this article and the article from which it was adapted were not supported by any external funding. During the peer review process, the manufacturer of the agent under review was offered an opportunity to comment on the articles. Changes resulting from comments received were made by the authors on the basis of scientific and editorial merit.
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The manuscript was reviewed by Emina Obarcanin, Sarajevo, Bosnia and Herzegovina.
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Lyseng-Williamson, K.A., McKeage, K. Once-Daily Memantine. Drugs Aging 30, 51–58 (2013). https://doi.org/10.1007/s40266-012-0041-0
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DOI: https://doi.org/10.1007/s40266-012-0041-0