Although the introduction of antipsychotic drugs in 1954 was a breakthrough
in the treatment of patients with schizophrenia, these agents have a numbe
r of adverse effects that limit effectiveness and compliance. The atypical
antipsychotic drugs provide an improved tolerability profile, particularly
in minimizing extrapyramidal side effects; however, they are associated wit
h significant weight gain, which may be related to growing evidence linking
the atypical agents with diabetes and hyperlipidemia. Ziprasidone, a new a
typical antipsychotic drug, was demonstrated in clinical trials to be more
efficacious than placebo and similar in efficacy to haloperidol in the trea
tment of schizophrenia. Like the existing atypical agents, ziprasidone has
a rate of extrapyramidal side effects similar to that of placebo and does n
ot cause significant elevations in prolactin levels. In contrast, ziprasido
ne has a low propensity for causing weight gain. For patients requiring an
antipsychotic drug, ziprasidone represents a new treatment option with a li
mited adverse effect profile.