Sertindole for schizophrenia
Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid
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Yn: Cochrane Database of Systematic Reviews, Cyfrol 2005, Rhif 3, CD001715, 20.07.2005.
Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid
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TY - JOUR
T1 - Sertindole for schizophrenia
AU - Lewis, Ruth
AU - Bagnall, Anne-Marie
AU - Leitner, Maria
PY - 2005/7/20
Y1 - 2005/7/20
N2 - This review includes three studies with a total of 1104 participants. We excluded two large important studies because they did not report any usable data. The three that were included suggested that sertindole (20 mg/day) was more antipsychotic than placebo, as acceptable as placebo (in terms of various adverse events including movement disorde r s and somnolence) and better tole r ated than haloperidol. Sertindole was associated with fewer movement disorders than h aloperidol, but was shown to cause more weight gainand the possible side e ffect of male sexual dysfunction. Cardiac problems (QTc intervals of at least 500 msec) were evident even in the randomised trials. Sertindole used at 16 mg/day (reported to be the most optimal dose by one study) caused more rhinitis than haloperidol.
AB - This review includes three studies with a total of 1104 participants. We excluded two large important studies because they did not report any usable data. The three that were included suggested that sertindole (20 mg/day) was more antipsychotic than placebo, as acceptable as placebo (in terms of various adverse events including movement disorde r s and somnolence) and better tole r ated than haloperidol. Sertindole was associated with fewer movement disorders than h aloperidol, but was shown to cause more weight gainand the possible side e ffect of male sexual dysfunction. Cardiac problems (QTc intervals of at least 500 msec) were evident even in the randomised trials. Sertindole used at 16 mg/day (reported to be the most optimal dose by one study) caused more rhinitis than haloperidol.
U2 - 10.1002/14651858.CD001715.pub2
DO - 10.1002/14651858.CD001715.pub2
M3 - Article
VL - 2005
JO - Cochrane Database of Systematic Reviews
JF - Cochrane Database of Systematic Reviews
SN - 1469-493X
IS - 3
M1 - CD001715
ER -