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Dexlansoprazole – a new-generation proton pump inhibitor

Dexlansoprazole modified release (MR) is an R-enantiomer of lansoprazole and a new-generation proton pump inhibitor exhibiting high efficacy in the treatment of symptoms and lesions associated with erosive oesophagitis caused by gastroesophageal reflux disease (GERD). The dual release of the active...

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Detalles Bibliográficos
Autores principales: Skrzydło-Radomańska, Barbara, Radwan, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697039/
https://www.ncbi.nlm.nih.gov/pubmed/26759624
http://dx.doi.org/10.5114/pg.2015.56109
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author Skrzydło-Radomańska, Barbara
Radwan, Piotr
author_facet Skrzydło-Radomańska, Barbara
Radwan, Piotr
author_sort Skrzydło-Radomańska, Barbara
collection PubMed
description Dexlansoprazole modified release (MR) is an R-enantiomer of lansoprazole and a new-generation proton pump inhibitor exhibiting high efficacy in the treatment of symptoms and lesions associated with erosive oesophagitis caused by gastroesophageal reflux disease (GERD). The dual release of the active ingredient – in the duodenum and the small intestine – makes it possible to achieve two peak concentrations at various times, within two and five hours of administration. Dexlansoprazole MR ensures the longest maintenance of drug concentration in the plasma of all known proton pump inhibitors, and the longest proton pump inhibitory effect. The basic indications for the drug include all forms of gastroesophageal reflux disease, especially with night-time heartburn and sleep disorders resulting from GERD. Dexlansoprazole can be taken regardless of meal times. It has a good safety profile and carries a low risk of adverse interactions with other drugs.
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spelling pubmed-46970392016-01-12 Dexlansoprazole – a new-generation proton pump inhibitor Skrzydło-Radomańska, Barbara Radwan, Piotr Prz Gastroenterol Review Paper Dexlansoprazole modified release (MR) is an R-enantiomer of lansoprazole and a new-generation proton pump inhibitor exhibiting high efficacy in the treatment of symptoms and lesions associated with erosive oesophagitis caused by gastroesophageal reflux disease (GERD). The dual release of the active ingredient – in the duodenum and the small intestine – makes it possible to achieve two peak concentrations at various times, within two and five hours of administration. Dexlansoprazole MR ensures the longest maintenance of drug concentration in the plasma of all known proton pump inhibitors, and the longest proton pump inhibitory effect. The basic indications for the drug include all forms of gastroesophageal reflux disease, especially with night-time heartburn and sleep disorders resulting from GERD. Dexlansoprazole can be taken regardless of meal times. It has a good safety profile and carries a low risk of adverse interactions with other drugs. Termedia Publishing House 2015-12-16 2015 /pmc/articles/PMC4697039/ /pubmed/26759624 http://dx.doi.org/10.5114/pg.2015.56109 Text en Copyright © 2015 Termedia http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Paper
Skrzydło-Radomańska, Barbara
Radwan, Piotr
Dexlansoprazole – a new-generation proton pump inhibitor
title Dexlansoprazole – a new-generation proton pump inhibitor
title_full Dexlansoprazole – a new-generation proton pump inhibitor
title_fullStr Dexlansoprazole – a new-generation proton pump inhibitor
title_full_unstemmed Dexlansoprazole – a new-generation proton pump inhibitor
title_short Dexlansoprazole – a new-generation proton pump inhibitor
title_sort dexlansoprazole – a new-generation proton pump inhibitor
topic Review Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697039/
https://www.ncbi.nlm.nih.gov/pubmed/26759624
http://dx.doi.org/10.5114/pg.2015.56109
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