Antipsychotic agents: efficacy and safety in schizophrenia

Arão Nogueira de Araújo,1 Eduardo Pondé de Sena,1,2 Irismar Reis de Oliveira,1,3 Mario F Juruena41Postgraduation Program in Interactive Processes of Organs and Systems, 2Department of Pharmacology, Institute of Health Sciences, 3Department of Neuroscience...

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Main Authors: de Araújo AN, de Sena EP, de Oliveira IR, Juruena MF
Format: Article
Language:English
Published: Dove Medical Press 2012-11-01
Series:Drug, Healthcare and Patient Safety
Online Access:http://www.dovepress.com/antipsychotic-agents-efficacy-and-safety-in-schizophrenia-a11635
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author de Araújo AN
de Sena EP
de Oliveira IR
Juruena MF
author_facet de Araújo AN
de Sena EP
de Oliveira IR
Juruena MF
author_sort de Araújo AN
collection DOAJ
description Arão Nogueira de Araújo,1 Eduardo Pondé de Sena,1,2 Irismar Reis de Oliveira,1,3 Mario F Juruena41Postgraduation Program in Interactive Processes of Organs and Systems, 2Department of Pharmacology, Institute of Health Sciences, 3Department of Neurosciences and Mental Health, School of Medicine, Federal University of Bahia, Salvador, Brazil; 4Stress and Affective Disorders Program, Department of Neuroscience and Behavior, Faculty of Medicine of Ribeirao Preto, University of Sao Paulo, Sao Paulo, BrazilAbstract: Antipsychotics have provided a great improvement in the management of people with schizophrenia. The first generation antipsychotics could establish the possibility of managing many psychotic subjects in an outpatient setting. With the advent of the second (SGA) and third generation antipsychotics (TGA), other psychiatric disorders such as bipolar depression, bipolar mania, autism, and major depressive disorder have now been approved for the use of these drugs for their treatment. Also, the administration of more specific assessment tools has allowed for better delineation of the repercussions of these drugs on symptoms and the quality of life of patients who use antipsychotic agents. In general, the SGA share similar mechanisms of action to achieve these results: dopamine-2 receptor antagonism plus serotonin-2A receptor antagonism. The TGA (eg, aripiprazole) have partial agonist activity at the dopamine-2 receptor site, and are also called dopaminergic stabilizers. The pharmacological profile of SGA and TGA may provide better efficacy against negative symptoms, and are less likely to produce extrapyramidal symptoms; however, the SGA and TGA are associated with many other adverse events. The clinician has to balance the risks and benefits of these medications when choosing an antipsychotic for an individual patient.Keywords: antipsychotic agents, schizophrenia, pharmacology, safety
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spelling doaj.art-850aae9fa3de4ad99a76e174955aa41a2022-12-21T22:08:52ZengDove Medical PressDrug, Healthcare and Patient Safety1179-13652012-11-012012default173180Antipsychotic agents: efficacy and safety in schizophreniade Araújo ANde Sena EPde Oliveira IRJuruena MFArão Nogueira de Araújo,1 Eduardo Pondé de Sena,1,2 Irismar Reis de Oliveira,1,3 Mario F Juruena41Postgraduation Program in Interactive Processes of Organs and Systems, 2Department of Pharmacology, Institute of Health Sciences, 3Department of Neurosciences and Mental Health, School of Medicine, Federal University of Bahia, Salvador, Brazil; 4Stress and Affective Disorders Program, Department of Neuroscience and Behavior, Faculty of Medicine of Ribeirao Preto, University of Sao Paulo, Sao Paulo, BrazilAbstract: Antipsychotics have provided a great improvement in the management of people with schizophrenia. The first generation antipsychotics could establish the possibility of managing many psychotic subjects in an outpatient setting. With the advent of the second (SGA) and third generation antipsychotics (TGA), other psychiatric disorders such as bipolar depression, bipolar mania, autism, and major depressive disorder have now been approved for the use of these drugs for their treatment. Also, the administration of more specific assessment tools has allowed for better delineation of the repercussions of these drugs on symptoms and the quality of life of patients who use antipsychotic agents. In general, the SGA share similar mechanisms of action to achieve these results: dopamine-2 receptor antagonism plus serotonin-2A receptor antagonism. The TGA (eg, aripiprazole) have partial agonist activity at the dopamine-2 receptor site, and are also called dopaminergic stabilizers. The pharmacological profile of SGA and TGA may provide better efficacy against negative symptoms, and are less likely to produce extrapyramidal symptoms; however, the SGA and TGA are associated with many other adverse events. The clinician has to balance the risks and benefits of these medications when choosing an antipsychotic for an individual patient.Keywords: antipsychotic agents, schizophrenia, pharmacology, safetyhttp://www.dovepress.com/antipsychotic-agents-efficacy-and-safety-in-schizophrenia-a11635
spellingShingle de Araújo AN
de Sena EP
de Oliveira IR
Juruena MF
Antipsychotic agents: efficacy and safety in schizophrenia
Drug, Healthcare and Patient Safety
title Antipsychotic agents: efficacy and safety in schizophrenia
title_full Antipsychotic agents: efficacy and safety in schizophrenia
title_fullStr Antipsychotic agents: efficacy and safety in schizophrenia
title_full_unstemmed Antipsychotic agents: efficacy and safety in schizophrenia
title_short Antipsychotic agents: efficacy and safety in schizophrenia
title_sort antipsychotic agents efficacy and safety in schizophrenia
url http://www.dovepress.com/antipsychotic-agents-efficacy-and-safety-in-schizophrenia-a11635
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