戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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
13 onths) than with quetiapine (4.0 months) and ziprasidone (2.8 months).
14 , quetiapine=125, risperidone=124, UC=30 and ziprasidone=32), 4 of which were conference abstracts an
15                                              Ziprasidone (40 to 160 mg per day) was included after it
16 io to 3 weeks of double-blind treatment with ziprasidone (40-80 mg twice daily) or placebo.
17 =63]; risperidone, 1.5-6.0 mg/day [N=69]; or ziprasidone, 40-160 mg/day [N=135]).
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
20 mean daily doses were 129.9 mg (SD=27.3) for ziprasidone and 11.3 mg (SD=2.8) for olanzapine.
21                   During 6 weeks' treatment, ziprasidone and olanzapine demonstrated comparable antip
22 pared 1-year mortality rates associated with ziprasidone and olanzapine in real-world use.
23 rs compared the efficacy and tolerability of ziprasidone and olanzapine in the treatment of acutely i
24 le and CGI severity scale scores between the ziprasidone and placebo groups.
25 gs (olanzapine, quetia-pine, risperidone, or ziprasidone) and followed for up to 18 months.
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
28  66 risperidone, olanzapine, quetiapine, and ziprasidone arms including 7264 patients.
29                                              Ziprasidone as an adjunct to escitalopram demonstrated a
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
33                                              Ziprasidone does prolong the QT interval, but there is n
34 ssigned in a 1:1 ratio to receive adjunctive ziprasidone (escitalopram plus ziprasidone, N=71) or adj
35 e, perphenazine, quetiapine, risperidone, or ziprasidone for up to 18 months.
36                        The escitalopram plus ziprasidone group also showed significantly greater impr
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
39 nificantly greater for the escitalopram plus ziprasidone group.
40 ne, quetiapine, olanzapine, risperidone, and ziprasidone, have been reported to preferentially increa
41                                              Ziprasidone hydrochloride was included after its approva
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
46            Only widespread use will prove if ziprasidone is entirely safe.
47                                              Ziprasidone, like many BCS Class II drugs with low intri
48                                              Ziprasidone monotherapy was significantly superior to pl
49 , patients were randomly assigned to receive ziprasidone (N=136) or olanzapine (N=133).
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
52                                          The Ziprasidone Observational Study of Cardiac Outcomes (ZOD
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
59 up, but not in the perphenazine (P=0.021) or ziprasidone (P=0.028) group.
60                                              Ziprasidone produced rapid, sustained improvements relat
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
63                 Quetiapine, risperidone, and ziprasidone use were not associated with the warning.
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.
67                                              Ziprasidone was well tolerated and associated with a low
68                          Olanzapine, but not ziprasidone, was associated with significant increases i
69                         Differences favoring ziprasidone were observed in metabolic parameters.
70 long-acting injection (risperidone LAI), and ziprasidone--were used to identify a cohort of 24 FDA-re

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。