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A review of ramelteon in the treatment of sleep disorders

Ramelteon is a selective melatonin receptor (MT(1) and MT(2)) agonist that has been approved by the US Food and Drug Administration for the treatment of insomnia characterized by difficulty with sleep onset. It is the only approved sleep-promoting medication that does not have a direct sedating effe...

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Detalles Bibliográficos
Autor principal: Neubauer, David N
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2515902/
https://www.ncbi.nlm.nih.gov/pubmed/18728808
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author Neubauer, David N
author_facet Neubauer, David N
author_sort Neubauer, David N
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description Ramelteon is a selective melatonin receptor (MT(1) and MT(2)) agonist that has been approved by the US Food and Drug Administration for the treatment of insomnia characterized by difficulty with sleep onset. It is the only approved sleep-promoting medication that does not have a direct sedating effect, but rather enhances sleep through effects on sleep regulatory mechanisms within the suprachiasmatic nucleus. Ramelteon has been shown to have no abuse liability and therefore is not scheduled by the U.S. Drug Enforcement Agency as a controlled substance. It is available as an 8 mg tablet, which should be taken approximately 30 minutes prior to bedtime. The FDA approval contains no limitation on how long the medication may be prescribed.
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spelling pubmed-25159022008-08-26 A review of ramelteon in the treatment of sleep disorders Neubauer, David N Neuropsychiatr Dis Treat Expert Opinion Ramelteon is a selective melatonin receptor (MT(1) and MT(2)) agonist that has been approved by the US Food and Drug Administration for the treatment of insomnia characterized by difficulty with sleep onset. It is the only approved sleep-promoting medication that does not have a direct sedating effect, but rather enhances sleep through effects on sleep regulatory mechanisms within the suprachiasmatic nucleus. Ramelteon has been shown to have no abuse liability and therefore is not scheduled by the U.S. Drug Enforcement Agency as a controlled substance. It is available as an 8 mg tablet, which should be taken approximately 30 minutes prior to bedtime. The FDA approval contains no limitation on how long the medication may be prescribed. Dove Medical Press 2008-02 2008-02 /pmc/articles/PMC2515902/ /pubmed/18728808 Text en © 2008 Dove Medical Press Limited. All rights reserved
spellingShingle Expert Opinion
Neubauer, David N
A review of ramelteon in the treatment of sleep disorders
title A review of ramelteon in the treatment of sleep disorders
title_full A review of ramelteon in the treatment of sleep disorders
title_fullStr A review of ramelteon in the treatment of sleep disorders
title_full_unstemmed A review of ramelteon in the treatment of sleep disorders
title_short A review of ramelteon in the treatment of sleep disorders
title_sort review of ramelteon in the treatment of sleep disorders
topic Expert Opinion
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2515902/
https://www.ncbi.nlm.nih.gov/pubmed/18728808
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