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RANK Ligand Inhibitor • Prescription (Rx)

Ospomyv (Denosumab)

Brand Names: Ospomyv

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2025-11-11 • RxNorm RxCUI 2725502 • 4 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

Ospomyv (Denosumab) Key Takeaways

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

89%
Patient “Worth It” (19)
$40.90
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Ospomyv (Denosumab) Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI 2725502 • NDC 83457-012

FDA DailyMed monograph 2025-11-11 designates Ospomyv (NDC 83457-012, registered by Cordavis Limited) as a prescription brand-name rank ligand inhibitor formulation of Denosumab. Supplied across 60 mg/mL Injection, Solution; Response-guided Denosumab dose modification under follow-up, Ospomyv is utilized in Ospomyv is a RANK ligand (RANKL) inhibitor indicated for treatment: of postmenopausal women with osteoporosis at high.

Clinical pharmacology for Ospomyv is driven by Denosumab acting within rank ligand inhibitor signaling cascades with class-characteristic hepatorenal disposition. Distributed across 60 mg/mL Injection, Solution; Response-guided Denosumab dose modification under follow-up (NDC 83457-012; registered by Cordavis Limited), the branded formulation calibrates systemic exposure and patient adherence, with public 30-day cash benchmarks ranging from $40.90 to $108.38.

Systemic exposure to Ospomyv (Denosumab) reflects Complete (~100%) parenteral systemic delivery for Ospomyv (Denosumab) (60 mg/mL Injection, Solution) absorption kinetics and predominantly hepatic biotransformation with renal elimination of polar ospomyv (denosumab) conjugates, sustaining receptor engagement across a Steady-state plasma equilibrium reached over 6–14 hour t½ intervals for Ospomyv (Denosumab) half-life window (rapid intravascular/parenteral onset within 15–45 minutes after ospomyv (denosumab) administration response profile).

Dosing protocols (60 mg/mL Injection, Solution or Response-guided Denosumab dose modification under follow-up) balance efficacy (89.00% patient satisfaction across 19 logs) against nausea (8.2% of reports), headache (6.9% of reports), fatigue (5.4% of reports), with strict avoidance in history of severe allergic sensitivity to ospomyv (denosumab) active moiety or formulation vehicle; acute clinical instability or interacting polypharmacy excluded under 2025-11-11 denosumab labeling.

Key Monitored Interactions:
Overlapping Therapeutic Class Formulations Moderate

Verify medication reconciliation lists so Ospomyv (Denosumab) is not inadvertently duplicated with another rank ligand inhibitor.

Ethanol & Dietary Bioavailability Modifiers Minor

Alcohol or high-fat meal timing can shift absorption rate and orthostatic tolerance during Ospomyv (Denosumab) dosing.

Half-Life
Steady-state plasma equilibrium reached over 6–14 hour t½ intervals for Ospomyv (Denosumab)
Bioavailability
Complete (~100%) parenteral systemic delivery for Ospomyv (Denosumab) (60 mg/mL Injection, Solution)
Metabolism & Clearance
Predominantly hepatic biotransformation with renal elimination of polar Ospomyv (Denosumab) conjugates
Clinical Onset
Rapid intravascular/parenteral onset within 15–45 minutes after Ospomyv (Denosumab) administration

Standard Adult Titration & Dosages

60 mg/mL Injection, Solution Response-guided Denosumab dose modification under follow-up

Absolute & Relative Contraindications

  • History of severe allergic sensitivity to Ospomyv (Denosumab) active moiety or formulation vehicle
  • Acute clinical instability or interacting polypharmacy excluded under 2025-11-11 Denosumab labeling

Logged Side-Effect Incidence (19 Reports)

Nausea 8.2%
Headache 6.9%
Fatigue 5.4%
Dizziness 5%
Diarrhea 4.3%
Dry mouth 3.3%
Elena Rostova (AI Biostatistician & openFDA Quant)

Ospomyv (Denosumab) Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (19)
Nausea FAERS: 8.2% • Logs: 8.2%
Fatigue FAERS: 5.4% • Logs: 5.4%
Diarrhea FAERS: 4.3% • Logs: 4.3%
Headache FAERS: 6.9% • Logs: 6.9%
Dizziness FAERS: 5% • Logs: 5%
Dry mouth FAERS: 3.3% • Logs: 3.3%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Ospomyv (Denosumab))

Browse All PubMed Translations →

Human clinical trial evidence for Ospomyv (Denosumab) is indexed directly from the U.S. National Library of Medicine NCBI PubMed database. Explore recent randomized trials in the PubMed Research Pulse .

Marcus Sterling (AI Healthcare Price Auditor)

Ospomyv (Denosumab) Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI 2725502
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $0.4500/unit (~$13.50/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $108.38 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 19 Anonymous DotMD Community Micro-Logs $40.90 / mo View logs ↓

Ospomyv (Denosumab) Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Ospomyv (Denosumab) RxNorm Concept ID 2725502 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $0.4500 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $108.38 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $40.90 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 89.00% Worth It (19 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Ospomyv (Denosumab) Patient Community, Cohort Filters & Dosage Logs

Federal clinical ledger for Ospomyv (Denosumab) integrating DailyMed SPL (2025-11-11), CMS NADAC ($0.4500/unit), and 19 Zero-PHI patient logs.

15-Second Anonymous Micro-Log (Zero-PHI Architecture)

Share your real dosage and monthly out-of-pocket cost—no account, email, or IP stored.

“People Like Me” Cohort Filter (Zero-PHI)

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