Sh. Preskorn, COMPARISON OF THE TOLERABILITY OF BUPROPION, FLUOXETINE, IMIPRAMINE, NEFAZODONE, PAROXETINE, SERTRALINE, AND VENLAFAXINE, The Journal of clinical psychiatry, 56, 1995, pp. 12-21
Drug development in psychiatry has evolved from a process dependent on
chance discovery to one based on rationally targeting specific mechan
isms of action believed to be important in the pathophysiology underly
ing psychiatric syndromes. Antidepressant pharmacotherapy is the first
area to have substantially benefited from this evolution. Serotonin s
elective reuptake inhibitors (SSRIs) were the first class of psychiatr
ic medications developed based on such molecular targeting. Nefazodone
is a new antidepressant that combines blockade of the serotonin-2 rec
eptor with serotonin uptake inhibition. Perhaps as a result of this du
al action, nefazodone caused fewer complaints of nervousness (e.g., ag
itation, anxiety), insomnia, and tremors and a higher incidence of con
fusion, dizziness, and vision disturbance than do other advanced gener
ation antidepressants based on several different ways of assessing the
relative incidence of these adverse effects. Reports of sexual dysfun
ction on nefazodone and bupropion treatment were tower than on treatme
nt with other recently released antidepressants.