Can the dose of Invega Sustenna (paliperidone) be increased from 156 mg?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: September 15, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Maximum Dose of Invega Sustenna (Paliperidone Palmitate)

The maximum approved dose of Invega Sustenna (paliperidone palmitate) is 234 mg (150 mg eq.), which is higher than the 156 mg dose mentioned in the question.

Dosing Information for Invega Sustenna

Invega Sustenna is available in multiple dose strengths, with the following options:

  • 39 mg (25 mg eq.)
  • 78 mg (50 mg eq.)
  • 117 mg (75 mg eq.)
  • 156 mg (100 mg eq.)
  • 234 mg (150 mg eq.)

Recommended Dosing Protocol

  1. Initiation regimen:

    • Day 1: 234 mg (150 mg eq.) administered in the deltoid muscle
    • Day 8: 156 mg (100 mg eq.) administered in the deltoid muscle
    • No oral supplementation is required with this regimen
  2. Monthly maintenance dosing:

    • Range: 39-234 mg (25-150 mg eq.)
    • Recommended dose: 117 mg (75 mg eq.)
    • Can be administered in either deltoid or gluteal muscle

Dose Adjustment Considerations

When considering dose increases above 156 mg:

  • Dose adjustments should be based on clinical response and tolerability
  • Increases should not occur more frequently than every 4 weeks
  • If increasing from 156 mg to 234 mg, monitor for:
    • Extrapyramidal symptoms
    • Hyperprolactinemia
    • Sedation
    • Weight gain
    • Potential cardiovascular effects

Special Populations

  • Renal impairment: Dose adjustments required for mild renal impairment (CrCl 50-80 mL/min)
  • Elderly patients: Same dosage as younger adults with normal renal function, but adjust if age-related decline in renal function occurs

Pharmacokinetic Considerations

The pharmacokinetic profile of paliperidone palmitate is biphasic:

  • Initial relatively fast zero-order input allows rapid attainment of therapeutic concentrations
  • Subsequent maintained second-stage, first-order input allows for monthly administration

Clinical Implications of Dosing

Higher doses may be associated with:

  • Increased risk of adverse effects including tachycardia, hypotension, QT prolongation, and extrapyramidal symptoms 1
  • Potentially improved symptom control in patients with inadequate response to lower doses

Conclusion

For patients currently on 156 mg of Invega Sustenna who require dose escalation, the maximum available dose is 234 mg (150 mg eq.) administered monthly. This should be considered only after evaluating the patient's clinical response to the current dose and weighing the potential benefits against increased risk of side effects.

References

Research

Need for Bioequivalence Standards that Reflect the Clinical Importance of the Complex Pharmacokinetics of Paliperidone Palmitate Long-Acting Injectable Suspension.

Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques, 2019

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.