Cochrane Database of Systematic Reviews 2000
DOI: 10.1002/14651858.cd001715
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Sertindole for schizophrenia

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Cited by 19 publications

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“…[24][25][26] Owing to its pharmacological profile, sertindole demonstrated efficacy in treating positive, negative, and cognitive symptoms, 27,[39][40][41][42][43][44]47,48 a low potential to cause sedation and EPS, 9,71 ) and an acceptable metabolic profile. Sertindole has a high affinity for serotonin 5-HT2A and 5-HT2C and α1 adrenergic receptors; its affinity for dopamine D2 receptors is more pronounced in limbic rather than nigrostriatal system.…”
Section: Results
mentioning
confidence: 99%
“…Studies comparing sertindole with risperidone showed a significantly lower incidence of EPS among sertindole-treated patients. 17 Similar to other atypical antipsychotics, sertindole induced a significant greater mean weight gain versus placebo and haloperidol 9,41,42,71 ; when compared with risperidone, both treatments were associated with a moderate increase in weight gain and body mass index but with no increased risk of metabolic syndrome. 41 The favorable profile of sertindole on EPS was confirmed by the meta-analysis of Leucht et al, which showed that sertindole (mean ORs, 0.17-0.2) produced fewer EPS than placebo and almost all other drugs and was preceded in ranking only by clozapine (mean ORs, 0.06-0.40).…”
Section: Adverse Events
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confidence: 97%
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