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This medicine is a selective serotonin reuptake inhibitor (SSRI) used to treat depression, panic disorder, obsessive-compulsive disorder (OCD), post-traumatic stress disorder (PTSD), social anxiety disorder (social phobia), and a severe form of premenstrual syndrome called premenstrual dysphoric disorder (PMDD).

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Generic form zoloft ) for the most common symptoms of bipolar disorder. Mood stabilization is a primary goal of treatment for a substantial number of patients with bipolar disorder, yet many have to struggle for months or years to achieve a stable mood. It is not known whether the antidepressant fluoxetine improves mood stabilization or if it is just a placebo effect. To investigate this issue, we conducted a double-blind placebo-controlled trial. This double-blind placebo-controlled trial was designed as a phase 1 multicenter trial to evaluate whether fluoxetine, an active pharmaceutical agent (CNS), could stabilize mood in bipolar patients treated for two weeks with standard therapy alone or lithium valproate (or any of the combination agents). All patients were treated for two weeks with either lithium or valproate the combination agents. Two weeks' treatment was split equally between the generics pharmacy price list of medicines subjects (at 10% of total weekly dose). All the subjects were screened for inclusion. In total, 14 subjects participated the study; mean age was 46, and the average duration of illness for the subjects was 7 years. Fourteen who participated in the study completed full two-week treatment period (12 individuals completed the treatment phase and one patient refused to continue). All patients provided written informed consent regarding their participation in the study and received treatment after receiving a comprehensive medical history and laboratory evaluation. A significant reduction of the Hamilton Anxiety Rating Scale ( HAMD-21 ) score was observed after two weeks of treatment with fluoxetine as compared to placebo (placebo + fluoxetine, p < 0.01). The results of open-label phase (10 patients in the fluoxetine + lithium valproate combination group) revealed that a significant difference was found in HAMD-21 and the Hamilton Rating Scale for Depression between the patients treated with fluoxetine (6.1 +/- 2.7 SD units) (placebo + lithium valproate, p < 0.01) and the comparison subjects (placebo + valproate, p < Acetanilide buy 0.01, lithium + valproate, p < 0.05). No clinical differences were observed between these groups. No other significant group differences were noted as assessed by the HAMD-21 and Hamilton Rating Scale for Depression (Table ). The most significant result found was that patients received treatment with fluoxetine showed a significant improvement in the number of patients experiencing atypical antipsychotic activity (p < 0.05 for treatment and p < 0.01 for response). A significant improvement in the number of patients experiencing adverse effects antipsychotic drugs was not observed (p > 0.10 for treatment and p < 0.05 for response) (Table ). The results of open-label phase are shown in Table. Discussion The goal of this study was to evaluate the effects of a single 5-week treatment with.

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