- Adherence benefits (potential for improved adherence, delayed onset of nonadherence)
- Earlier detection of nonadherence (allows for rapid intervention, helps differentiate nonadherence from poor medication efficacy)
- Simplification of medication routine (eliminates daily dosing of oral medications, fewer day-to-day reminders of illness)
- Pharmacokinetics/pharmacodynamics properties (more stable serum concentrations reduce side effects and symptoms related to peak and trough plasma concentrations, greater flexibility in dosing scheduling due to long half-life, reduced risk of withdrawal symptoms or symptom exacerbation)
- Possibility of attaining lowest effective dose with step-wise reduction
- Reduced risk of medication overdose
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- Do not solve all adherence issues (due to patient refusal or discontinuation of LAIAs)
- Negative patient perception of LAIAs (stigma, coercion, or use as a tracking method)
- Lack of availability of LAI formulations/fewer medication options than oral antipsychotics
- Pharmacokinetics/pharmacodynamics properties (conversion from oral to LAIAs may be challenging, initiation may require initial oral supplementation, lack of flexibility in changing/adjusting doses, not immediately reversible if adverse effects develop)
- Possible injection-site reactions
- Risk of post-injection delirium/sedation syndrome (olanzapine)
- Higher direct medication cost of LAIAs compared with oral formulations
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