The FDA is requiring a boxed warning be added to conventional antipsychotics to explain an increased risk of death in elderly
patients treated for dementia-related psychosis. This decision is a follow-up to a similar labeling change made in 2005 for atypical
antipsychotic drugs. Both conventional and atypical antipsychotics are approved for the treatment of symptoms associated with schizophrenia;
neither is approved for use to treat dementia-related symptoms.