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1 pears to be efficacious for nonresponders to nefazodone, and nefazodone appears to be effective for C
2                  In addition, trovafloxacin, nefazodone, and ritonavir were reported to be associated
3 RI) antidepressants (bupropion, mirtazapine, nefazodone, and venlafaxine), tricyclic antidepressants,
4 cacious for nonresponders to nefazodone, and nefazodone appears to be effective for CBASP nonresponde
5 when they are administered with fluvoxamine, nefazodone, fluoxetine, and sertraline.
6 the rates of response were 55 percent in the nefazodone group and 52 percent in the psychotherapy gro
7 pped out of the study prematurely, 22 in the nefazodone group and 8 in the CBASP group.
8 factory response) was 48 percent in both the nefazodone group and in the psychotherapy group, as comp
9                        Adverse events in the nefazodone group were consistent with the known side eff
10 new-generation non-SSRI antidepressants (eg, nefazodone hydrochloride, mirtazapine, bupropion hydroch
11                                              Nefazodone is a weaker serotonin and norepinephrine reup
12 der to 12 weeks of outpatient treatment with nefazodone (maximal dose, 600 mg per day), the cognitive
13  have been recently introduced: venlafaxine, nefazodone, mirtazapine, and reboxetine.
14 lopram, fluoxetine, imipramine, mirtazapine, nefazodone, nortriptyline, paroxetine, sertraline, and v
15 response to short-term treatment with either nefazodone or a cognitive behavioral-analysis system of
16 ater risks of hepatotoxicity are iproniazid, nefazodone, phenelzine, imipramine, amitriptyline, dulox
17 e to CBASP and the switch from from CBASP to nefazodone resulted in clinically and statistically sign
18                                      Because nefazodone seems to cause severe hepatocellular injury i
19 mistries should be performed before starting nefazodone therapy and patients should be monitored regu
20 temporal onset of disease after the start of nefazodone therapy suggested severe hepatocellular injur
21       However, the switch to CBASP following nefazodone therapy was associated with significantly les
22 at sample revealed that both the switch from nefazodone to CBASP and the switch from from CBASP to ne
23 ts (selective serotonin reuptake inhibitors, nefazodone, venlafaxine, and mirtazapine) in participant
24                                The dosage of nefazodone was 100 to 600 mg/d; CBASP was provided twice
25                                              Nefazodone was administered for 14 to 28 weeks before th

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