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RANK Ligand Inhibitor • Prescription (Rx)

Osvyrti (Denosumab-Desu)

Brand Names: Osvyrti

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-07-07 • RxNorm RxCUI 2746871 • 4 Linked .gov / PubMed Citations • Governance: Dr. Devon Caldwell, DO, MPH (NPI #1568063758)
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

Osvyrti (Denosumab-Desu) Key Takeaways

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

81%
Patient “Worth It” (16)
$103.54
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Osvyrti (Denosumab-Desu) Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI 2746871 • NDC 69448-021

Within the RANK Ligand Inhibitor category, Osvyrti provides branded delivery of active pharmaceutical ingredient Denosumab-Desu (registered by Accord BioPharma Inc.; NDC 69448-021). Characterized by 60 mg/mL Injection; Longitudinal Osvyrti (Denosumab-Desu) dosing interval tailored to tolerability under 2026-07-07 SPL documentation, Osvyrti targets 1 Indications and usage osvyrti: is a RANK ligand (RANKL) inhibitor indicated for: of postmenopausal women with.

Through its Denosumab-Desu active moiety, Osvyrti exerts rank ligand inhibitor activity with class-characteristic hepatorenal disposition. Registered under NDC 69448-021 (registered by Accord BioPharma Inc.; effective 2026-07-07), the 60 mg/mL Injection; Longitudinal Osvyrti (Denosumab-Desu) dosing interval tailored to tolerability presentation ensures reproducible pharmacokinetic release profiles documented in federal RxNorm (2746871) and CMS NADAC ($1.3200/unit) ledgers.

With Terminal t½ estimated at 7–19 hrs depending on renal/hepatic reserve (Osvyrti (Denosumab-Desu)) residence kinetics and Complete (~100%) parenteral systemic delivery for Osvyrti (Denosumab-Desu) (60 mg/mL Injection) bioavailability, Osvyrti (Denosumab-Desu) undergoes mixed metabolic conjugation and unchanged urinary excretion across osvyrti (denosumab-desu) regimens and establishes therapeutic activity over rapid intravascular/parenteral onset within 15–45 minutes after osvyrti (denosumab-desu) administration.

Standard adult regimens span 60 mg/mL Injection, Longitudinal Osvyrti (Denosumab-Desu) dosing interval tailored to tolerability. Prescribers screen specifically against severe drug-induced hypersensitivity to denosumab-desu or inactive tablet/vehicle binders; prohibited co-prescriptions or physiological states specified in fda spl 2026-07-07 for osvyrti (denosumab-desu), while community micro-logs most frequently note nausea (8.2% of reports), headache (8% of reports), dizziness (6.6% of reports).

Key Monitored Interactions:
Hepatically Conjugated Concomitant Therapies Moderate

Assess baseline hepatic panels and interacting prescriptions when starting Osvyrti (Denosumab-Desu) (rank ligand inhibitor).

Ethanol & Dietary Bioavailability Modifiers Minor

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

Half-Life
Terminal t½ estimated at 7–19 hrs depending on renal/hepatic reserve (Osvyrti (Denosumab-Desu))
Bioavailability
Complete (~100%) parenteral systemic delivery for Osvyrti (Denosumab-Desu) (60 mg/mL Injection)
Metabolism & Clearance
Mixed metabolic conjugation and unchanged urinary excretion across Osvyrti (Denosumab-Desu) regimens
Clinical Onset
Rapid intravascular/parenteral onset within 15–45 minutes after Osvyrti (Denosumab-Desu) administration

Standard Adult Titration & Dosages

60 mg/mL Injection Longitudinal Osvyrti (Denosumab-Desu) dosing interval tailored to tolerability

Absolute & Relative Contraindications

  • Severe drug-induced hypersensitivity to Denosumab-Desu or inactive tablet/vehicle binders
  • Prohibited co-prescriptions or physiological states specified in FDA SPL 2026-07-07 for Osvyrti (Denosumab-Desu)

Logged Side-Effect Incidence (16 Reports)

Nausea 8.2%
Headache 8%
Dizziness 6.6%
Fatigue 6.2%
Diarrhea 5.8%
Dry mouth 5.1%
Elena Rostova (AI Biostatistician & openFDA Quant)

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

openFDA / Label % Patient Logs (16)
Nausea FAERS: 8.2% • Logs: 8.2%
Fatigue FAERS: 6.2% • Logs: 6.2%
Diarrhea FAERS: 5.8% • Logs: 5.8%
Headache FAERS: 8% • Logs: 8%
Dizziness FAERS: 6.6% • Logs: 6.6%
Dry mouth FAERS: 5.1% • Logs: 5.1%
Dr. Lin (AI PubMed Clinical Trial Lead)

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

Browse All PubMed Translations →

Human clinical trial evidence for Osvyrti (Denosumab-Desu) 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)

Osvyrti (Denosumab-Desu) Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI 2746871
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $1.3200/unit (~$39.60/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $274.38 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 16 Anonymous DotMD Community Micro-Logs $103.54 / mo View logs ↓

Osvyrti (Denosumab-Desu) Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Osvyrti (Denosumab-Desu) RxNorm Concept ID 2746871 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $1.3200 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $274.38 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $103.54 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 81.00% Worth It (16 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Osvyrti (Denosumab-Desu) Patient Community, Cohort Filters & Dosage Logs

Evidence synthesis for Osvyrti (Denosumab-Desu): FDA labeling (2026-07-07, NDC 69448-021), CYP/interaction screening, and public pharmacy acquisition costs.

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

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

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