Alzheimer's disease (AD) primarily results in memory impairment and co
gnitive deficits in areas such as language, visuospatial function, cal
culation, praxis and judgement. However, over 30% of patients with dem
entia develop a group of secondary behavioural disturbances, including
depression, hallucinations and delusions, agitation, insomnia and wan
dering. Because these secondary symptoms impair patients' function, in
crease their need far supervision, and often influence the decision to
institutionalise them, the control of these symptoms is a priority in
managing AD. Psychotropic drugs, particularly antipsychotics (neurole
ptics), have been a mainstay in treating many of these symptoms, but c
arry a high risk of adverse effects. Patients with AD may be particula
rly vulnerable to adverse effects of medications because of changes in
pharmacokinetics and neurotransmitter systems, related to both AD and
aging. At present, treating secondary symptoms of AD is more of an ar
t than a science. For virtually every group of symptoms, older and new
er classes of medications are available, with proven efficacy in patie
nts without dementia and less clear results in AD patients. We review
current treatment options and suggest preferences for each symptom com
plex, based on a trade-off between efficacy and adverse effects. New a
gents, such as selective serotonin reuptake inhibitors and atypical an
ti-psychotics, may herald the arrival of symptom- (and receptor-) spec
ific drugs with minimal adverse effects. Until the appropriate trials
are conducted in patients with AD, including comparative studies of di
fferent agents, we recommend that clinicians select and use a few medi
cations from the suggestions in this review, know their pharmacokineti
c and half-life profiles in depth, and follow the general principles t
hat apply to using any medication in elderly patients.