These drugs are dopamine antagonists as they block dopamine activity within 48 hours, and this seems to be why they are therapeutic for people with schizophrenia.
FGAs are effective in reducing positive symptoms for many people, but as many as 40% gain no relief at all and many people still experience negative symptoms.
FGAs also have unpleasant side effects, such as stiff or slow movements of your face that you can’t control (tardive dyskinesia), sleepiness/tiredness, weight gain, problems with sex drive and low blood pressure.
Clozapine blocks dopamine in the same way as FGAs but additionally acts on serotonin and glutamate receptors, for example blocking serotonin receptors (having an antagonist effect)
Antipsychotic drugs are considered more humane as it meant that people with the diagnosis of schizophrenia had the chance to remain in the community instead of being kept in isolation in institutions.
The main weakness of drug therapy is that it isn’t a cure, it just temporarily reduces the symptoms; as soon as the patient stops taking them, the symptoms return, usually within 3-6 weeks.
Guo et al (2011) carried out research into the effectiveness of antipsychotics in China and found few significant differences when they compared 7 antipsychotics.
Drug treatment for schizophrenia rests on strong biological evidence about the causes of schizophrenia (e.g dopamine hypothesis) so is underpinned by theory.
Zhao (2016) conducted a meta-analysis comparing 18 antipsychotics and found that 17 of the antipsychotics tested had significantly lower relapse rates than placebos.
Although SGA’s cause fewer side-effects, one major side effect is the fatal blood condition agranulocytosis which has led to this drug falling out in favour though it is still used with treatment-resistant clients, providing relief for up to 60% of such people.
Patel et al (2014), in a review on the efficacy of medication for schizophrenia, explains that it is important to start medication use quickly in order to be most effective.
In the first 7 days following a psychotic episode, the objective is to decrease hostility and to attempt to return the client to normal functioning (e.g sleeping and eating)
Once the symptoms have begun to subside, a maintenance dose will be prescribed to encourage socialisation, self-care and improve mood and combat relapse.
Meltzer et al (2004) choose 481 patients with schizophrenia and randomly assigned them into groups where one group had a placebo, investigational drugs, and haloperidol (FGA)