BOXED WARNING Increased mortality in elderly patients with dementia-related psychosis treated with antipsychotic drugs; INVEGA HAFYERA is not approved for use in patients with dementia-related psychosis.
FDA dosing
Population
Start
Target
Max
Schizophrenia, after adequate treatment with once-monthly paliperidone palmitate (PP1M) for ≥4 months or every-3-month (PP3M) for ≥1 cycle
Adults
Based on prior product: 1,092 mg (from PP1M 156 mg or PP3M 546 mg) or 1,560 mg (from PP1M 234 mg or PP3M 819 mg)
Gluteal IM injection once every 6 months
Renal Mild (CrCl 50–<80): stabilize on PP1M first, then transition; moderate or severe (CrCl <50): not recommended
Hepatic Undefined
Administered once every 6 months
Instructions
Initiate only after adequate treatment with PP1M ≥4 months or PP3M ≥1 three-month cycle
Gluteal IM injection by a healthcare professional once every 6 months
When switching from PP1M, the two preceding injection cycles should be the same strength
Contraindications
Known hypersensitivity to paliperidone, risperidone, or to any excipients in INVEGA HAFYERA
Cautions
Cerebrovascular adverse reactions in elderly with dementia-related psychosis
Pregnancy Third-trimester exposure risks neonatal extrapyramidal and/or withdrawal symptoms; epidemiologic data have not established a drug-associated risk of major birth defects
Lactation Paliperidone present in human milk; monitor breastfed infant for sedation, failure to thrive, jitteriness, and extrapyramidal symptoms
⚠ BOXED WARNING
Increased mortality in elderly patients with dementia-related psychosis