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Serotonin-selective reuptake additional indications

Preliminary findings indicate that the addition of fluoxetine may increase response or benefit treatment-resistant schizophrenic patients ( 367, 368 and 369). Further, deficit symptoms seemed to improve in some patients, supporting a possible role for 5-FIT2 hypersensitivity as the underlying mechanism 370). Care must be taken to monitor plasma levels of antipsychotics, which may rise when combined with this selective serotonin reuptake inhibitor (SSRI) or other related antidepressants due to their ability to inhibit various CYP 450 isoenzymes. [Pg.78]

The selective serotonin reuptake inhibitors (SSRIs) represent a chemically diverse class of agents that have as their primary action the inhibition of the serotonin transporter (SERT) (Figure 30-3). Fluoxetine was introduced in the United States in 1988 and quickly became one of the most commonly prescribed medications in medical practice. The development of fluoxetine emerged out of the search for chemicals that had high affinity for monoamine receptors but lacked the affinity for histamine, acetylcholine, and adrenoceptors that is seen with the tricyclic antidepressants (TCAs). There are currently six available SSRIs, and they are the most common antidepressants in clinical use. In addition to their use in major depression, SSRIs have indications in GAD, PTSD, OCD, panic disorder, PMDD, and bulimia. Fluoxetine, sertraline, and citalopram exist as isomers and are formulated in the racemic forms, whereas paroxetine and fluvoxamine are not optically active. Escitalopram is the S enantiomer of citalopram. As with all antidepressants,... [Pg.652]

Fluoxetine (Prozac /Lilly), paroxetine (Paxil /GlaxoSmithKilne), and sertraline (Zoloft /Pfizer) are selective serotonin reuptake inhibitors (SSRIs) and are useful in the treatment of depression. These agents potentiate the pharmacological actions of the neurotransmitter serotonin by preventing its reuptake at presynaptic neuronal membranes. In addition to its SSRI properties, venlafaxine (EfFexor /Wyeth-Ayerst) also appears to be a potent inhibitor of neuronal norepinephrine reuptake and a weak inhibitor of dopamine reuptake thereby enhancing the actions of these neurotransmitters as well. Venlafaxine is indicated for use in anxiety and depression. [Pg.418]


See other pages where Serotonin-selective reuptake additional indications is mentioned: [Pg.534]    [Pg.153]    [Pg.730]    [Pg.20]    [Pg.691]    [Pg.245]    [Pg.26]   
See also in sourсe #XX -- [ Pg.6 , Pg.490 ]




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