During the past decade, treatment options for depression have increased wit
h the introduction of new agents. Older agents, such as tricyclic antidepre
ssants and monoamine oxidase inhibitors, increase noradrenergic and seroton
ergic neurotransmission. Attempts to separate antidepressant effects from a
dverse effects led to the development of selective serotonin reuptake inhib
itors (SSRIs). Citalopram is the newest SSRI to be marketed in the United S
tates. Of all SSRIs on the market, it is the most selective for serotonin r
euptake pump. Its efficacy in treating depression was evident in both place
bo-controlled and comparator trials. In addition, citalopram was studied in
the treatment of other psychiatric disorders. The agent has less inhibitio
n of cytochrome P450 enzymes than other SSRIs, possibly giving it a lower p
otential for drug interactions.