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Safety and tolerability of antipsychotics: focus on amisulpride

The introduction of the atypical antipsychotic drugs represents an important advance in the treatment of schizophrenia, because the therapeutic efficacy, tolerability, and safety profiles of these agents seem to be superior to that of the classical neuroleptics. As would be predicted from the pharma...

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Autores principales: Juruena, Mario F, de Sena, Eduardo Pondé, de Oliveira, Irismar Reis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108712/
https://www.ncbi.nlm.nih.gov/pubmed/21701632
http://dx.doi.org/10.2147/DHPS.S6226
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author Juruena, Mario F
de Sena, Eduardo Pondé
de Oliveira, Irismar Reis
author_facet Juruena, Mario F
de Sena, Eduardo Pondé
de Oliveira, Irismar Reis
author_sort Juruena, Mario F
collection PubMed
description The introduction of the atypical antipsychotic drugs represents an important advance in the treatment of schizophrenia, because the therapeutic efficacy, tolerability, and safety profiles of these agents seem to be superior to that of the classical neuroleptics. As would be predicted from the pharmacologic profile of a pure D(2)/D(3) receptor blocker, amisulpride is an atypical antipsychotic agent, effective for positive and negative symptoms, which can bring about additional improvement in the social functioning and quality of life of patients with schizophrenia. Amisulpride is effective in acute schizophrenia as determined by Clinical Global Impression scores. The major concern regarding the safety of the atypical antipsychotics is related to their propensity to induce weight gain and alter glucose and lipid metabolism. Amisulpride has one of the lowest potentials for weight gain of all the antipsychotic agents, and is associated with clearly lower use of antiparkinsonian medication and with fewer dropouts due to adverse events than conventional antipsychotics. Amisulpride is well tolerated with regard to anxiety and insomnia, and not notably different from placebo. Amisulpride has a pronounced prolactin-elevating effect which appears to be independent of dosage and duration of administration. Hyperprolactinemia rapidly reverses following amisulpride discontinuation. Amisulpride benefits patients with negative symptoms, and is the only antipsychotic to demonstrate efficacy in patients with predominantly negative symptoms. Amisulpride maintains its efficacy when used for medium/long-term treatment, as demonstrated in studies of up to 12 months. In terms of relevance of the effects, superiority is observed for quality of life, social adaptation, and functioning, as measured by the Quality of Life and Functional Status Questionnaire scales. In conclusion, amisulpride is an antipsychotic agent with proven efficacy and good tolerability. Moreover, this drug can help people with schizophrenia to attain social reinsertion.
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spelling pubmed-31087122011-06-23 Safety and tolerability of antipsychotics: focus on amisulpride Juruena, Mario F de Sena, Eduardo Pondé de Oliveira, Irismar Reis Drug Healthc Patient Saf Review The introduction of the atypical antipsychotic drugs represents an important advance in the treatment of schizophrenia, because the therapeutic efficacy, tolerability, and safety profiles of these agents seem to be superior to that of the classical neuroleptics. As would be predicted from the pharmacologic profile of a pure D(2)/D(3) receptor blocker, amisulpride is an atypical antipsychotic agent, effective for positive and negative symptoms, which can bring about additional improvement in the social functioning and quality of life of patients with schizophrenia. Amisulpride is effective in acute schizophrenia as determined by Clinical Global Impression scores. The major concern regarding the safety of the atypical antipsychotics is related to their propensity to induce weight gain and alter glucose and lipid metabolism. Amisulpride has one of the lowest potentials for weight gain of all the antipsychotic agents, and is associated with clearly lower use of antiparkinsonian medication and with fewer dropouts due to adverse events than conventional antipsychotics. Amisulpride is well tolerated with regard to anxiety and insomnia, and not notably different from placebo. Amisulpride has a pronounced prolactin-elevating effect which appears to be independent of dosage and duration of administration. Hyperprolactinemia rapidly reverses following amisulpride discontinuation. Amisulpride benefits patients with negative symptoms, and is the only antipsychotic to demonstrate efficacy in patients with predominantly negative symptoms. Amisulpride maintains its efficacy when used for medium/long-term treatment, as demonstrated in studies of up to 12 months. In terms of relevance of the effects, superiority is observed for quality of life, social adaptation, and functioning, as measured by the Quality of Life and Functional Status Questionnaire scales. In conclusion, amisulpride is an antipsychotic agent with proven efficacy and good tolerability. Moreover, this drug can help people with schizophrenia to attain social reinsertion. Dove Medical Press 2010-10-01 /pmc/articles/PMC3108712/ /pubmed/21701632 http://dx.doi.org/10.2147/DHPS.S6226 Text en © 2010 Juruena et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Juruena, Mario F
de Sena, Eduardo Pondé
de Oliveira, Irismar Reis
Safety and tolerability of antipsychotics: focus on amisulpride
title Safety and tolerability of antipsychotics: focus on amisulpride
title_full Safety and tolerability of antipsychotics: focus on amisulpride
title_fullStr Safety and tolerability of antipsychotics: focus on amisulpride
title_full_unstemmed Safety and tolerability of antipsychotics: focus on amisulpride
title_short Safety and tolerability of antipsychotics: focus on amisulpride
title_sort safety and tolerability of antipsychotics: focus on amisulpride
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108712/
https://www.ncbi.nlm.nih.gov/pubmed/21701632
http://dx.doi.org/10.2147/DHPS.S6226
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