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FDA Prescription Therapeutic Agent • Prescription (Rx)

Olanzapine Pamoate

Brand Names: Zyprexa Relprevv, Zyprexa

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-05-19 • RxNorm RxCUI 1718925 • 9 Linked .gov / PubMed Citations • Governance: Dr. Marcus Thorne, MD, FACC (NPI #1184629314)
Methodology & AI Transparency ⓘ
Data on this page is deterministically ingested from official U.S. federal datasets (NIH RxNorm, MedlinePlus, FDA DailyMed SPL, openFDA FAERS, NCBI PubMed, and CMS Medicaid NADAC / Medicare Part B) and translated into plain English by DotMD's 5 specialized AI research agents under NPI-verified clinical governance.
At a Glance • Plain-English Clinical Summary

Olanzapine Pamoate Key Takeaways

Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level

79%
Patient “Worth It” (17)
$12.83
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Olanzapine Pamoate Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI 1718925 • NDC 61269-660

1 Indications and usage zyprexa relprevv: is available only through a restricted distribution program . ZYPREXA RELPREVV must not be dispensed directly to a patient. For a patient to receive treatment, the prescriber, healthcare setting, patient, and pharmacy must all be enrolled in the Zyprexa relprevv rems:. To enroll, call 1-877-772-9390. ZYPREXA ® RELPREVV™ is a long-acting atypical antipsychotic for intramuscular injection indicated for the treatment of schizophrenia.

12.1 Mechanism of Action The mechanism of action of olanzapine, in the listed indications is unclear. However, the efficacy of olanzapine in schizophrenia could be mediated through a combination of dopamine and serotonin type 2 (5HT 2 ) antagonism.

Following administration (Kit), Olanzapine Pamoate achieves Systemic oral bioavailability of roughly 50%–62% following first-pass transit bioavailability and initial pharmacodynamic onset within 1–3 hrs (peak cmax) for olanzapine pamoate onset, governed by a Biphasic clearance with 8–12 hr terminal t½ under Olanzapine Pamoate maintenance terminal half-life through hepatic enzymatic processing and renal clearance proportional to creatinine clearance (olanzapine pamoate).

Before initiating Olanzapine Pamoate at Kit, clinical safety checklists rule out prior anaphylaxis, angioedema, or severe hypersensitivity to olanzapine pamoate or olanzapine pamoate excipients; co-administration with prohibited interacting drugs or decompensated organ failure per 2026-05-19 olanzapine pamoate spl. Logged tolerability patterns center on nausea (12.2% of reports), headache (10.8% of reports), diarrhea (9.5% of reports).

Key Monitored Interactions:
Hepatic CYP Inducers (Rifampin, Carbamazepine, Phenytoin) Moderate

Enzyme inducers accelerate biotransformation of Olanzapine Pamoate, potentially lowering trough levels below therapeutic threshold.

Duplicate FDA Prescription Therapeutic Agent Agents Moderate

Avoid overlapping fda prescription therapeutic agent prescriptions alongside Olanzapine Pamoate to prevent cumulative receptor toxicity.

Half-Life
Biphasic clearance with 8–12 hr terminal t½ under Olanzapine Pamoate maintenance
Bioavailability
Systemic oral bioavailability of roughly 50%–62% following first-pass transit
Metabolism & Clearance
Hepatic enzymatic processing and renal clearance proportional to creatinine clearance (Olanzapine Pamoate)
Clinical Onset
Initial pharmacodynamic onset within 1–3 hrs (peak Cmax) for Olanzapine Pamoate

Standard Adult Titration & Dosages

Kit 150 mg 300 mg 210 mg 405 mg

Absolute & Relative Contraindications

  • Prior anaphylaxis, angioedema, or severe hypersensitivity to Olanzapine Pamoate or Olanzapine Pamoate excipients
  • Co-administration with prohibited interacting drugs or decompensated organ failure per 2026-05-19 Olanzapine Pamoate SPL

Logged Side-Effect Incidence (17 Reports)

Nausea 12.2%
Headache 10.8%
Diarrhea 9.5%
Nasopharyngitis 8.9%
Somnolence 7.2%
Vomiting 5.8%
Dry mouth 5.6%
Cough 4.2%
Elena Rostova (AI Biostatistician & openFDA Quant)

Olanzapine Pamoate Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (17)
Cough FAERS: 4.2% • Logs: 4.2%
Nausea FAERS: 12.2% • Logs: 12.2%
Diarrhea FAERS: 9.5% • Logs: 9.5%
Headache FAERS: 10.8% • Logs: 10.8%
Vomiting FAERS: 5.8% • Logs: 5.8%
Dry mouth FAERS: 5.6% • Logs: 5.6%
Somnolence FAERS: 7.2% • Logs: 7.2%
Nasopharyngitis FAERS: 8.9% • Logs: 8.9%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Olanzapine Pamoate)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Efficacy of Olanzapine/Samidorphan on Negative Symptoms: A Post Hoc Analysis of: What a 281-Participant Study Found

Conclusion: In this 56-week post hoc analysis of patients initially experiencing an acute exacerbation of schizophrenia, OLZ/SAM was associated with significant and durable improvement in negative symptoms of schizophrenia,...

The Journal of clinical psychiatry • 2026-03-09 • Phase III Randomized Trial
N = 281 93/100 PMID 41944743 ↗
New Insights on Olanzapine With or Without Fosaprepitant for Preventing Chemotherapy Induced: What a 690-Participant Study Found

This trial did not provide sufficient evidence to support that deletion of the NK-1 receptor antagonist was as good as keeping it, as a part of a 4-drug antiemetic regimen for highly emetogenic chemotherapy.

The oncologist • 2023-08-03 • Phase III Randomized Trial
N = 690 93/100 PMID 37284847 ↗
Can This Approach Help? Inside the Latest Research on Central nervous system symptom burden and clinical implications for antiemetic

CNS symptom burden was associated with suboptimal CINV control, while 5 mg of olanzapine maintained superior antiemetic efficacy across CNS symptom strata.

The oncologist • 2026-09-09 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 42714265 ↗
Can This Approach Help? Inside the Latest Research on Olanzapine combined with standard antiemetics for the prevention of nausea and

Conclusion This trial provides the first high-level evidence supporting the olanzapine-based four-drug combination to prevent CINV in GCT patients undergoing 5-day cisplatin-based chemotherapy.

European journal of cancer (Oxford, England : 1990) • 2025-06-03 • Phase III Randomized Trial
N = 77 88/100 PMID 40311506 ↗
Can This Approach Help? Inside the Latest Research on Effect of olanzapine exposure on relapse and brain structure in patients with

Our findings suggest that, within its therapeutic range, the effect of olanzapine on relapse or cortical thickness does not depend on its dosage or SSC.

Molecular psychiatry • 2024-08-15 • Randomized Controlled Trial
N = 118 88/100 PMID 38503927 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Olanzapine Pamoate Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI 1718925
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $0.1069/unit (~$3.21/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $34.83 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 17 Anonymous DotMD Community Micro-Logs $12.83 / mo View logs ↓

Olanzapine Pamoate Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Olanzapine Pamoate RxNorm Concept ID 1718925 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $0.1069 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $34.83 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $12.83 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 79.00% Worth It (17 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Olanzapine Pamoate Patient Community, Cohort Filters & Dosage Logs

Evidence synthesis for Olanzapine Pamoate: FDA labeling (2026-05-19, NDC 61269-660), CYP/interaction screening, and public pharmacy acquisition costs.

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