Amisulpride: a Brief Review.

dc.contributor.authorChhabra, Vishal
dc.contributor.authorBhatia, Manjeet Singh
dc.date.accessioned2015-05-07T04:09:10Z
dc.date.available2015-05-07T04:09:10Z
dc.date.issued2007-10
dc.description.abstractAmisulpride, belonging to second generation antipsychotics, is a substituted benzamide derivative indicated for the treatment of acute and chronic schizophrenia with prominent positive and/or negative symptoms. Amisulpride has high affinity for the dopamine D2/D3 receptors. It inhibits dopamine transmission by blocking postsynaptic D2/D3 receptors in the limbic system, which is predicative of potent antipsychotic activity. The elimination half-life is 12 hours. Metabolism is limited with most of the drug excreted unchanged in the feces (64%). Clinical studies have supported that Amisulpride (400-1200mg/day) is at least as effective as Haloperidol and Risperidone and more effective than flupenthixol in acute exacerbation. In the treatment of patients with predominantly negative symptoms, Amisulpride was more effective than placebo. Recently some studies have shown it to be having efficacy in dysthymia also. Its favorable characteristics also include low incidence of EPSE and weight gain, however, it has a high incidence of prolactin elevation.en_US
dc.identifier.citationChhabra Vishal, Bhatia Manjeet Singh. Amisulpride: a Brief Review. Delhi Psychiatry Journal. 2007 Oct; 10 (2): 140-143.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/157992
dc.language.isoenen_US
dc.subject.meshDysthymic Disorder --drug therapy
dc.subject.meshHumans
dc.subject.meshSchizophrenia --drug therapy
dc.subject.meshSulpiride --administration & dosage
dc.subject.meshSulpiride --adverse effects
dc.subject.meshSulpiride --analogs and derivatives
dc.subject.meshSulpiride --pharmacology
dc.subject.meshSulpiride --pharmacokinetics
dc.titleAmisulpride: a Brief Review.en_US
dc.typeArticleen_US
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