Jantoven (Warfarin Sodium)
Brand Names: Jantoven
Methodology & AI Transparency ⓘ
Jantoven (Warfarin Sodium) Key Takeaways
Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level
- 1 What it does: As a proprietary vitamin k antagonist presentation registered by Upsher-Smith Laboratories, LLC, Jantoven supplies active moiety Warfarin Sodium (cross-referenced at /meds/warfarin-sodium) in 2.5 mg/1 Tablet; 4 mg/1 Tablet (NDC 0832-1213, 0832-1215; SPL 2026-08-10).
- 2 Real-world patient consensus: Registered under RxNorm 855296-B08321213 and SPL 2026-08-10, pairing Jantoven packaging with active ingredient Warfarin Sodium.
- 3 Typical cash cost range: Public pharmacy ledger: $14.36 low cash benchmark vs. $38.05 chain retail average ($0.0813/unit CMS NADAC).
- 4 Top reported side effects / signs: Key post-marketing and trial adverse reactions (Jantoven (Warfarin Sodium)): nausea (9.2%), headache (8.5%), dizziness (6.9%).
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Jantoven (Warfarin Sodium) Mechanism, CYP450 Pathways & DailyMed Monograph
As a proprietary vitamin k antagonist presentation registered by Upsher-Smith Laboratories, LLC, Jantoven supplies active moiety Warfarin Sodium (cross-referenced at /meds/warfarin-sodium) in 2.5 mg/1 Tablet; 4 mg/1 Tablet (NDC 0832-1213, 0832-1215; SPL 2026-08-10). Clinical prescribing and dispensing guidelines focus on Warfarin sodium tablets, USP are indicated for: Prophylaxis and treatment of venous thrombosis and its extension,.
The active constituent inside Jantoven—Warfarin Sodium—functions as a targeted vitamin k antagonist agent involving CYP2C9 clearance pathways. While therapeutic target engagement mirrors generic Warfarin Sodium, Jantoven (registered by Upsher-Smith Laboratories, LLC, SPL 2026-08-10) specifies proprietary packaging (0832-1213, 0832-1215) and 2.5 mg/1 Tablet; 4 mg/1 Tablet quality controls alongside a $0.0813/unit NADAC acquisition baseline.
Systemic exposure to Jantoven (Warfarin Sodium) reflects F ≈ 71%–83% systemic availability after standard oral Jantoven (Warfarin Sodium) administration absorption kinetics and jantoven (warfarin sodium) undergoes cyp2c9-mediated hepatic metabolism prior to excretion, sustaining receptor engagement across a Terminal t½ estimated at 7–17 hrs depending on renal/hepatic reserve (Jantoven (Warfarin Sodium)) half-life window (time to peak concentration spans 1 to 2 hrs under jantoven (warfarin sodium) maintenance response profile).
Dosing protocols (2.5 mg/1 Tablet or 4 mg/1 Tablet or 6 mg/1 Tablet or 1 mg/1 Tablet or 10 mg/1 Tablet) balance efficacy (93.00% patient satisfaction across 5 logs) against nausea (9.2% of reports), headache (8.5% of reports), dizziness (6.9% of reports), with strict avoidance in documented intolerance or hypersensitivity reaction involving warfarin sodium (vitamin k antagonist); concurrent restricted medications flagged in section 4/7 of the jantoven (warfarin sodium) dailymed monograph (855296-b08321213).
Concurrent Jantoven (Warfarin Sodium) exposure alters anticoagulant pharmacodynamics, requiring closer hemorrhagic surveillance.
Review concurrent CYP2C9 substrates and inhibitors when titrating Jantoven (Warfarin Sodium) maintenance doses.
Standard Adult Titration & Dosages
Absolute & Relative Contraindications
- Documented intolerance or hypersensitivity reaction involving Warfarin Sodium (vitamin k antagonist)
- Concurrent restricted medications flagged in Section 4/7 of the Jantoven (Warfarin Sodium) DailyMed monograph (855296-B08321213)
Logged Side-Effect Incidence (5 Reports)
Jantoven (Warfarin Sodium) Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs
Peer-Reviewed Human Clinical Trials & Meta-Analyses (Jantoven (Warfarin Sodium))
Human clinical trial evidence for Jantoven (Warfarin Sodium) is indexed directly from the U.S. National Library of Medicine NCBI PubMed database. Explore recent randomized trials in the PubMed Research Pulse .
Jantoven (Warfarin Sodium) Public Price Transparency Ledger
| Dispensing Channel / Benchmark | Verification Source | Reference Cost | Details |
|---|---|---|---|
| Pharmacy Acquisition Cost (CMS NADAC) | CMS Medicaid NADAC Weekly National Survey | $0.0813/unit (~$2.44/30u) | Wholesale baseline |
| Average U.S. Walk-In Retail Cash Price | Chain Pharmacy Uninsured Cash Index | $38.05 / mo | Before coupon/insurance |
| Patient-Logged Out-of-Pocket Average | 5 Anonymous DotMD Community Micro-Logs | $14.36 / mo | View logs ↓ |
Jantoven (Warfarin Sodium) Federal Verification & Benchmark Summary
| Metric | Verified Benchmark | Source |
|---|---|---|
| Jantoven (Warfarin Sodium) RxNorm Concept ID | 855296-B08321213 | U.S. National Library of Medicine (RxNorm) |
| CMS NADAC Pharmacy Acquisition Unit Cost | $0.0813 / unit | CMS Medicaid NADAC Weekly Feed |
| Walk-In Chain Pharmacy Cash Average | $38.05 / mo | U.S. Uninsured Retail Cash Index |
| Public Mail-Order Wholesale Benchmark | $14.36 / mo (Patient Mean) | Public Cash Reference |
| Real-World Patient Consensus | 93.00% Worth It (5 anonymous logs) | DotMD Zero-PHI Patient Ledger |
Jantoven (Warfarin Sodium) Patient Community, Cohort Filters & Dosage Logs
Evidence synthesis for Jantoven (Warfarin Sodium): FDA labeling (2026-08-10, NDC 0832-1213), CYP/interaction screening, and public pharmacy acquisition costs.
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