Atypical antipsychotics


Atypical antipsychotics
Atypical antipsychotic drugs are agents designed to treat schizophrenia. They include aripiprazole, clozapine, olanzapine, paliperidone, quetiapine, risperidone, and ziprasidone.
Pharmacokinetics
Atypical antipsychotics are absorbed after oral administration.
Metabolism and excretion
Atypical antipsychotics are metabolized by the liver. Metabolites of clozapine, olanzapine, quetiapine, and ziprasidone are inactive, whereas risperidone and paliperidone have active metabolites. They’re highly plasma protein-bound and eliminated in urine, with a small portion eliminated in stool.
Pharmacodynamics
Atypical antipsychotics typically block the dopamine receptors, but to a lesser extent than the typical antipsychotics, resulting in far fewer extrapyramidal adverse effects. Additionally, atypical antipsychotics block serotonin receptor activity.
Putting it together
These combined actions account for their effectiveness against the positive and negative symptoms of schizophrenia with minimal extrapyramidal effects.
Pharmacotherapeutics
Atypical antipsychotics are considered the first line of treatment for patients with schizophrenia because of equal or improved effectiveness combined with improved tolerability.
Lower doses do for dementia
Atypical antipsychotics are commonly used to treat behavioral and psychotic symptoms in patients with dementia. Dosages are significantly lower for these patients than for patients with schizophrenia.
Drug interactions
Drugs that alter the P-450 enzyme system alter the metabolism of some atypical antipsychotics.
The straight “dopa”
Atypical antipsychotics counteract the effects of levodopa and other dopamine agonists. 

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