What is the equivalent dose of Zyprexa Relprevv (olanzapine pamoate) for a patient currently taking oral Zyprexa (olanzapine)?

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: December 20, 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.

Conversion from Oral Olanzapine to Zyprexa Relprevv (Olanzapine Pamoate)

Use the established conversion table where oral olanzapine 10 mg daily converts to Zyprexa Relprevv 210 mg every 2 weeks or 405 mg every 4 weeks, with proportional adjustments for other oral doses. 1

Standard Conversion Algorithm

The conversion from oral olanzapine to the long-acting injectable formulation follows a structured dosing equivalence:

Conversion Table

  • Oral olanzapine 10 mg/day → Zyprexa Relprevv 210 mg every 2 weeks OR 405 mg every 4 weeks 1
  • Oral olanzapine 15 mg/day → Zyprexa Relprevv 300 mg every 2 weeks OR 405 mg every 4 weeks 1
  • Oral olanzapine 20 mg/day → Zyprexa Relprevv 300 mg every 2 weeks 1

Key Conversion Principles

The long-acting injection is administered without oral supplementation once steady-state is achieved, as demonstrated in pivotal trials where OLAI efficacy was established without concurrent oral olanzapine. 1

For doses between standard conversions, round to the nearest available depot strength (150 mg, 210 mg, 300 mg, or 405 mg) based on clinical response. 1

Critical Safety Considerations

Post-injection syndrome occurs in <0.1% of injections but requires mandatory observation for at least 3 hours post-injection by qualified healthcare personnel in a healthcare facility. 1 This risk management plan is non-negotiable and must be followed for every injection. 1

Monitoring Requirements

  • Observe patient for minimum 3 hours after each injection 1
  • Monitor for sedation, delirium, extrapyramidal symptoms, dysarthria, ataxia, aggression, dizziness, weakness, hypertension, and convulsion 1
  • Ensure patient does not drive or operate machinery for remainder of the day 1

Practical Implementation

Start with the equivalent depot dose based on the conversion table above, administered every 2 or 4 weeks depending on the selected formulation. 1 The every-2-week and every-4-week formulations have different pharmacokinetic profiles, so selection should be based on patient preference and adherence patterns. 1

Oral olanzapine supplementation is not required during the transition period or maintenance, as the depot formulation provides adequate therapeutic levels when dosed appropriately. 1

Common Pitfalls to Avoid

  • Do not continue oral olanzapine supplementation indefinitely—the depot formulation alone is sufficient for maintenance therapy 1
  • Do not discharge patients immediately after injection—the 3-hour observation period is mandatory 1
  • Do not use in patients who cannot comply with the post-injection monitoring requirements 1

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.