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1.
J Clin Psychiatry ; 60(6): 400-6, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10401920

ABSTRACT

BACKGROUND: The long-term efficacy and tolerability of the antidepressant reboxetine, a unique selective norepinephrine reuptake inhibitor (selective NRI), were assessed in an international study. METHOD: Two hundred eighty-three patients with recurrent DSM-III-R major depression who responded to 6 weeks of reboxetine treatment (> or =50% decrease in Hamilton Rating Scale for Depression [HAM-D] total score) were randomly assigned to receive reboxetine or placebo for 46 weeks in a double-blind phase. Relapse (> or =50% increase in HAM-D total score and/or a HAM-D total score > or =18) rate was the principal assessment criterion and included patients who experienced relapse or recurrence. Only patients who remained relapse-free at the end of the first 6-month treatment period were included in the relapse rate assessment at the end of the second 6-month treatment period. RESULTS: Reboxetine was associated with a markedly lower relapse rate than placebo (22% vs. 56%; p<.001) and a greater cumulative probability of a maintained response (p = .0001) during long-term treatment. Patients in remission (HAM-D total score < or =10) at the time of random assignment were less likely to relapse (16% reboxetine, 48% placebo; p<.001). The proportion of patients who were relapse-free and therefore remained in the study was significantly (p< or =.001) higher among those on reboxetine treatment than on placebo at the end of the first (61% vs. 40%) and second (88% vs. 59%) 6 months of treatment. Additional efficacy measures supported these findings. The incidence of adverse events with reboxetine was low and comparable with that for placebo. Discontinuation due to adverse events occurred infrequently. CONCLUSION: Reboxetine treatment over 1 year is more effective than placebo in the prevention of relapse in patients with recurrent depression. The low relapse rates at the end of the second 6 months of treatment further suggest that reboxetine effectively prevents recurrence of depressive symptoms following episode resolution. Reboxetine is well tolerated in long-term treatment of depression, a finding that bodes well for long-term patient compliance.


Subject(s)
Adrenergic Uptake Inhibitors/therapeutic use , Depressive Disorder/prevention & control , Morpholines/therapeutic use , Adult , Depressive Disorder/drug therapy , Depressive Disorder/psychology , Double-Blind Method , Female , Follow-Up Studies , Humans , Longitudinal Studies , Male , Norepinephrine , Patient Dropouts , Placebos , Psychiatric Status Rating Scales/statistics & numerical data , Reboxetine , Secondary Prevention , Treatment Outcome
2.
Int Pharmacopsychiatry ; 10(3): 149-56, 1975.
Article in English | MEDLINE | ID: mdl-1158629

ABSTRACT

In 15 normal volunteers the action of succinic semialdehyde (SSA), and in 24 volunteers the effect of sodium succinate (SS), on the HNA have been investigated. As a result it was found that SSA brings about some enhancement of the excitatory process in cortical - mainly verbal -activities, accompanied by subjective improvement of memory and concentration. In the other hand, the administration of SS improves the stability of cortical excitatory process and its equilibrium with cortical inhibition; and enhances the connecting activity of the verbal system. These changes parallel the subjective elevation of mood and of general tone. In the basis of this study, one may suggest that succinic acid may be a psychoenergizer. The task of further investigations is to establish the range of therapeutic activity of these compounds.


Subject(s)
Higher Nervous Activity/drug effects , Succinates/pharmacology , Adult , Aldehydes/adverse effects , Aldehydes/pharmacology , Attention/drug effects , Female , Humans , Learning/drug effects , Male , Memory/drug effects , Reflex/drug effects , Self-Assessment , Succinates/adverse effects , Time Factors , Word Association Tests
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