Introduction
Paliperidone is the primary active metabolite of risperidone. The mechanism of action is unknown but it is likely to act via a similar pathway to risperidone. It has been proposed that the drug's therapeutic activity in schizophrenia is mediated through a combination of central dopamine Type 2 (D2) and serotonin Type 2 (5HT2A) receptor antagonism. Paliperidone is also active as an antagonist at alpha 1 and alpha 2 adrenergic receptors and H1 histaminergic receptors, which may explain some of the other effects of the drug.
Uses
Paliperidone is an atypical antipsychotic used in the treatment of schizophrenia and other schizoaffective or delusional disorders.
For the treatment of schizophrenia.
Associated Conditions
Pharmacodynamics
Paliperidone is an atypical antipsychotic developed by Janssen Pharmaceutica. Chemically, paliperidone is primary active metabolite of the older antipsychotic risperidone (paliperidone is 9-hydroxyrisperidone). The mechanism of action is unknown but it is likely to act via a similar pathway to risperidone.
Mechanism of Action
Paliperidone is the major active metabolite of risperidone. The mechanism of action of paliperidone, as with other drugs having efficacy in schizophrenia, is unknown, but it has been proposed that the drug's therapeutic activity in schizophrenia is mediated through a combination of central dopamine Type 2 (D2) and serotonin Type 2 (5HT2A) receptor antagonism.
Absorption
The absolute oral bioavailability of paliperidone following paliperidone administration is 28%.
Volume of Distribution
- 487 L
Protein Binding
The plasma protein binding of racemic paliperidone is 74%.
Route of Elimination
One week following administration of a single oral dose of 1 mg immediate-release 14C-paliperidone to 5 healthy volunteers, 59% (range 51% – 67%) of the dose was excreted unchanged into urine, 32% (26% – 41%) of the dose was recovered as metabolites, and 6% – 12% of the dose was not recovered.
Half Life
The terminal elimination half-life of paliperidone is approximately 23 hours.
Toxicity
The possibility of obtundation, seizures, or dystonic reaction of the head and neck following overdose may create a risk of aspiration with induced emesis.
Food Interactions
- Avoid alcohol.
Dosage
- Initiation Dosing: Day 1-234 mg and Day 8-156 mg
- Monthly Maintenance Dose: 39-234 mg
- Maximum Monthly Dose: 234 mg
- Initiation Dosing: Day 1-234 mg and Day 8-156 mg
- Monthly Maintenance Dose: 78-234 mg
- Maximum Monthly Dose: 234 mg