Since the introduction of chlorpromazine in the 1950s, neuroleptic med
ications have been the mainstay of treatment of schizophrenia and othe
r psychotic disorders. These medications do not always lead to complet
e remission of symptoms but they have allowed many patients to lead mo
re productive and satisfying lives away from the restrictions of chron
ic hospitalisation. However, neuroleptics are associated with a number
of adverse effects that can compromise their effectiveness. Extrapyra
midal adverse effects include acute dystonic reactions, neuroleptic-in
duced Parkinsonism and akathisia. They can often be treated with neuro
leptic dose reduction, addition of anticholinergic or beta-blocking ag
ents, or medication change. Later-onset movement disorders such as tar
dive dyskinesia or dystonia require careful evaluation and may be trea
ted with dose reduction or change of neuroleptic to an atypical agent.
Potentially fatal reactions such as agranulocytosis and neuroleptic m
alignant syndrome can rarely occur and often require significant medic
al intervention. Clozapine offers some advantages over 'typical' neuro
leptics but has a unique adverse effect profile which includes agranul
ocytosis.