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Expansion of guidance for the day 8 initiation dose of paliperidone palmitate to avoid a missed dose
Author(s) -
Mahesh N. Samtani,
Isaac Nuamah,
Srihari Gopal,
Remmerie,
Sliwa,
Larry Alphs
Publication year - 2013
Publication title -
neuropsychiatric disease and treatment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.819
H-Index - 67
eISSN - 1178-2021
pISSN - 1176-6328
DOI - 10.2147/ndt.s40836
Subject(s) - paliperidone , medicine , paliperidone palmitate , dosing , regimen , tolerability , pharmacokinetics , pharmacology , antipsychotic , adverse effect , schizophrenia (object oriented programming) , psychiatry
Paliperidone palmitate (PP) is a long-acting injectable formulation of an atypical antipsychotic, paliperidone. Its dose can be expressed in milligram or milligram equivalents (mg eq) of active paliperidone (39, 78, 117, 156, and 234 mg of PP correspond to 25, 50, 75, 100, and 150 mg eq of paliperidone). The recommended initiation dosing regimen for PP is 150 [day 1]/100[day 8] mg eq. Labeling guidance allowed a ± 2 day window for the day 8 injection that provides more flexibility with patient scheduling and avoids missing the day 8 initiation dose. Recently, expansion of the day 8 dosing window from ±2 to ±4 days has been approved in the United States based on results obtained from the model-based simulations and review of safety data presented here.

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