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Dose response and atypical antipsychotics in schizophrenia

  • Bruce J. Kinon(corresponding author)
    ,
  • Jonna Ahl
    ,
  • Virginia L. Stauffer
    ,
  • Angela L. Hill
    ,
  • Peter F. Buckley
*Corresponding author for this work
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Based on information from clinical trials, both the efficacy and adverse effects of conventional antipsychotics in the treatment of schizophrenia are dose related. The overlapping nature of these dose-response profiles limits the use of these agents. Atypical antipsychotics provide greater relief across the comorbid symptom domains of schizophrenia, but dose-response studies and clinical experience have revealed that some of these drugs also have dose limitations. This article reviews the dose-response relationships of the atypical antipsychotics as presented predominantly in pivotal, randomised studies (double-blind and otherwise). Limited data indicate that clozapine shows dose-related efficacy up to 600 mg/ day in patients with treatment-resistant schizophrenia. However, higher dosages of clozapine may be associated with the risk of seizures. Risperidone demonstrates dose-related adverse events that compromise efficacy. The dose-response relationships for ziprasidone, quetiapine and aripiprazole are less well established. The efficacy of olanzapine appears to be dose related within the recommended dosage range of 10-20 mg/day, but clinical trials that have explored higher dosages suggest improved efficacy. Furthermore, the higher doses are not associated with a significantly increased incidence of adverse events. Further studies are clearly needed to fully characterise the dose-response relationships of atypical antipsychotics.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 597-616 (20 pages)

Journal (Volume, Issue Number)

CNS Drugs (Volume 18, Issue 9)

Publication milestones

  • Published - 2004

Publication status

Published - 2004

ISSN

1172-7047

Publication IDs

  • Scopus: 3242659711
  • PubMed: 15222776

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
1.97
SciVal
Author count
5
SciVal
citations
47
SciVal
Paper percentile
85
Fractional count
1
Fractional count
0.20
Fractional count
4
Fractional count
0.80
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Captures
39
Citation count
52

Funding Details

This work was funded by Eli Lilly and Company, Indianapolis, IN, USA. The authors have no conflicts of interest that are directly relevant to the content of this review.