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1 idepressant efficacy also favored adjunctive ziprasidone.
2 ne, olanzapine, quetiapine, risperidone, and ziprasidone.
3 efficacy versus haloperidol, quetiapine, and ziprasidone.
4 ment, in patients treated with quetiapine or ziprasidone.
5 eridone, and 79 percent of those assigned to ziprasidone.
6 ilar to that of quetiapine, risperidone, and ziprasidone.
7 these variables were significant and favored ziprasidone.
8 r other safety parameters were observed with ziprasidone.
9 ped antipsychotic drugs, e.g., clozapine and ziprasidone.
10 liorated by clozapine but not haloperidol or ziprasidone.
11 -0.14), olanzapine (-0.25, -0.39 to -0.12), ziprasidone (-0.25, -0.48 to -0.01), and risperidone (-0
12 14.0 [6.0-18.0] days) as did patients in the ziprasidone (15.0 [9.1-18.0] days) and placebo groups (1
14 , quetiapine=125, risperidone=124, UC=30 and ziprasidone=32), 4 of which were conference abstracts an
18 ne, quetiapine, olanzapine, risperidone, and ziprasidone all potently antagonize the beta-arrestin 2
19 antly increased with olanzapine but not with ziprasidone; all between-group comparisons of these vari
23 rs compared the efficacy and tolerability of ziprasidone and olanzapine in the treatment of acutely i
26 n, including thioridazine, mesoridazine, and ziprasidone, and for monitoring for signs of myocarditis
27 apine was more effective than quetiapine and ziprasidone, and risperidone was more effective than que
30 pine were more effective than quetiapine and ziprasidone as reflected by longer time until discontinu
31 idone, olanzapine, quetiapine, aripiprazole, ziprasidone, asenapine, iloperidone, or paliperidone) wi
32 y evaluated the efficacy and tolerability of ziprasidone, compared with placebo, in the treatment of
34 ssigned in a 1:1 ratio to receive adjunctive ziprasidone (escitalopram plus ziprasidone, N=71) or adj
37 sia, compared with six (20%) patients in the ziprasidone group and seven (19%) patients in the placeb
38 Ten (14%) patients in the escitalopram plus ziprasidone group discontinued treatment because of into
40 ne, quetiapine, olanzapine, risperidone, and ziprasidone, have been reported to preferentially increa
42 rs sought to test the efficacy of adjunctive ziprasidone in adults with nonpsychotic unipolar major d
43 red olanzapine, quetiapine, risperidone, and ziprasidone in patients who had just discontinued a diff
44 with olanzapine, quetiapine, risperidone, or ziprasidone in phase 1 or 1B of the trials, primarily be
45 e findings of this study failed to show that ziprasidone is associated with an elevated risk of nonsu
50 r of initiating pharmacotherapy was 0.91 for ziprasidone (N=9,077) and 0.90 for olanzapine (N=9,077).
51 ve adjunctive ziprasidone (escitalopram plus ziprasidone, N=71) or adjunctive placebo (escitalopram p
53 apine (odds ratio: 1.56, 95% CI: 1.47-1.67), ziprasidone (odds ratio: 1.40, 95% CI: 1.19-1.65), and f
54 , N=386), amisulpride (one study, N=331), or ziprasidone (one study, N=207) for a weighted mean and m
55 ly assigned to receive treatment with either ziprasidone or olanzapine and followed for 1 year by unb
56 randomly assigned to receive haloperidol or ziprasidone or placebo every 6 hrs for up to 14 days.
57 , the risk was higher among those initiating ziprasidone (OR, 1.61; 95% CI, 0.99-2.64; P = .06) and a
58 0.26 for risperidone (P<.001), and 0.12 for ziprasidone (P<.06), with no significant differences bet
61 e.g. clozapine, risperidone, olanzapine and ziprasidone, to improve cognitive function in schizophre
62 pite the known risk of QTc prolongation with ziprasidone treatment, the findings of this study failed
64 lafaxine, bupropion, quetiapine, olanzapine, ziprasidone, valproic acid, carbamazepine, and citalopra
65 der adults with schizophrenia, intramuscular ziprasidone was found to be effective, and evidence is e
66 set of action was rapid, and tolerability of ziprasidone was generally comparable to that of placebo.
70 long-acting injection (risperidone LAI), and ziprasidone--were used to identify a cohort of 24 FDA-re
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