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Serotonergic Adverse Events

Regarding side-effect profiles, all three SSNRIs are generally well tolerated, most adverse events occurring early in treatment, with a mild to moderate severity and a tendency to decrease or disappear with continued treatment. Venlafaxine (1) seems to be the least weU-toIerated SNRI, combining a higher level of serotonergic adverse events (nausea, sexual dysfunction, withdrawal problems) with dose-dependent hypertension. In contrast, milnacipran (2) and duloxetine (3) appear better tolerated and essentially devoid of cardiovascular toxicity. [Pg.203]

Medications with serotonergic activity may also have other monaminergic or sympathomimetic activity. Combining MAOIs with these medications may result in a complex side effect profile. For example, combining meperidine or dextromethorphan with MAOIs may result in respiratory depression, in addition to symptoms of serotonin excess. Furthermore, interactions between MAOIs and tricyclic antidepressants (TCAs) more commonly result in potentiating shared adverse events such as othostatic hypotension, as opposed to hyperadrenergic crises or the serotonin syndrome. [Pg.298]

Reboxetine is a nontricyclic SNRI in which the propylamine side chain of the TCAs is constrained into a morpholine ring (Fig. 21.8). It is a potent and selective ligand for the NET, with a mechanism of action is similar to that of desipramine. Reboxetine is used for the treatment of major depressive disorders. It is a chiral compound that is marketed as a racemic mixture of R,R- and S,S-reboxetine. The antidepressant activity for reboxetine appears to reside with the S,S-(+)-enantiomer, which has approximately twofold the inhibition potency of the R,R-enantiomer (42). It is well tolerated, with different adverse-event profiles, and it appears to be at least as effective as the SSRIs in the treatment of depressive illness. Currently, it is available only in Europe and is under U.S. FDA review. It preferentially inhibits the reuptake of NE (5-FIT NE ratio, 8). Reboxetine is not metabolized by the polymorphic isoforms, CYP2D6 or CYP2C19, and may offer a valuable alternative to the secondary amine TCAs in the treatment of major depression. Reboxetine is likely to become a promising alternative for patients who have failed treatment with or do not tolerate serotonergic antidepressants. Reboxetine has been shown to be effective and well tolerated in the treatment of panic... [Pg.828]

Concurrent use can be uneventful. A review of the safely of the combined use of lithium and the SSRIs identified 503 subjects who had received the combination without any evidence of serious adverse events. However, occasionally and unpredictably adverse reactions develop, but the precise incidence is not known. Most manufacturers of the SSRIs, and the US manufacturers of lithium, suggest that the combination of lithium and the SSRIs should be used with caution, and patients should be monitored closely. The UK manufacturers of lithium say that the combination may precipitate a serotonergic syndrome, which justifies immediate discontinuation of treatment. ... [Pg.1116]


See other pages where Serotonergic Adverse Events is mentioned: [Pg.163]    [Pg.774]    [Pg.134]    [Pg.163]    [Pg.204]    [Pg.821]    [Pg.839]    [Pg.864]    [Pg.172]    [Pg.407]    [Pg.416]    [Pg.425]    [Pg.434]    [Pg.440]    [Pg.449]    [Pg.249]    [Pg.484]    [Pg.493]    [Pg.502]    [Pg.511]    [Pg.517]    [Pg.526]   
See also in sourсe #XX -- [ Pg.203 ]




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Adverse events

Serotonergic

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