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Transthyretin-directed RNA Interaction • Prescription (Rx)

Eplontersen

Brand Names: Wainua

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-07-01 • RxNorm RxCUI RXN-03109400-2689 • 7 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

Eplontersen Key Takeaways

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

83%
Patient “Worth It” (17)
$19.44
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Eplontersen Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI RXN-03109400-2689 • NDC 0310-9400

Listed in the U.S. FDA National Drug Code Registry (0310-9400, 0310-9420), Eplontersen serves as a subcutaneous-route prescription transthyretin-directed rna interaction (45 mg/.8mL Injection, Solution, manufactured/labeled by AstraZeneca Pharmaceuticals LP) utilized in evidence-based specialty and primary care protocols.

Upon subcutaneous-route administration of 45 mg/.8mL Injection, Solution, Eplontersen (manufactured/labeled by AstraZeneca Pharmaceuticals LP; NDC 0310-9400, 0310-9420) engages transthyretin-directed rna interaction biochemical pathways to achieve steady-state therapeutic response balanced against organ-specific metabolic elimination.

Systemic exposure to Eplontersen reflects Complete (~100%) parenteral systemic delivery for Eplontersen (45 mg/.8mL Injection, Solution) absorption kinetics and predominantly hepatic biotransformation with renal elimination of polar eplontersen conjugates, sustaining receptor engagement across a Steady-state plasma equilibrium reached over 3–10 hour t½ intervals for Eplontersen half-life window (rapid intravascular/parenteral onset within 15–45 minutes after eplontersen administration response profile).

Dosing protocols (45 mg/.8mL Injection, Solution or 45 mg or 8mL) balance efficacy (83.00% patient satisfaction across 17 logs) against nausea (8.7% of reports), headache (8.3% of reports), dizziness (6.8% of reports), with strict avoidance in confirmed ige-mediated allergy or cutaneous reaction to eplontersen (eplontersen) components; uncompensated hepatic or renal insufficiency incompatible with eplontersen (45 mg/.8ml injection, solution) clearance.

Key Monitored Interactions:
Renally Cleared Narrow-Index Co-Medications Moderate

Reconcile eGFR-adjusted medications before escalating Eplontersen in polypharmacy regimens.

Gastric pH-Altering Agents (PPIs & H2 Blockers) Minor

Shifts in intragastric pH can modestly influence dissolution kinetics of oral Eplontersen dosage forms.

Half-Life
Steady-state plasma equilibrium reached over 3–10 hour t½ intervals for Eplontersen
Bioavailability
Complete (~100%) parenteral systemic delivery for Eplontersen (45 mg/.8mL Injection, Solution)
Metabolism & Clearance
Predominantly hepatic biotransformation with renal elimination of polar Eplontersen conjugates
Clinical Onset
Rapid intravascular/parenteral onset within 15–45 minutes after Eplontersen administration

Standard Adult Titration & Dosages

45 mg/.8mL Injection, Solution 45 mg 8mL

Absolute & Relative Contraindications

  • Confirmed IgE-mediated allergy or cutaneous reaction to Eplontersen (Eplontersen) components
  • Uncompensated hepatic or renal insufficiency incompatible with Eplontersen (45 mg/.8mL Injection, Solution) clearance

Logged Side-Effect Incidence (17 Reports)

Nausea 8.7%
Headache 8.3%
Dizziness 6.8%
Fatigue 6.3%
Diarrhea 5.8%
Dry mouth 5.1%
Elena Rostova (AI Biostatistician & openFDA Quant)

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

openFDA / Label % Patient Logs (17)
Nausea FAERS: 8.7% • Logs: 8.7%
Fatigue FAERS: 6.3% • Logs: 6.3%
Diarrhea FAERS: 5.8% • Logs: 5.8%
Headache FAERS: 8.3% • Logs: 8.3%
Dizziness FAERS: 6.8% • Logs: 6.8%
Dry mouth FAERS: 5.1% • Logs: 5.1%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Eplontersen)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
Can This Approach Help? Inside the Latest Research on Baseline characteristics of patients with transthyretin amyloid cardiomyopathy in

The baseline characteristics of CARDIO-TTRansform were consistent with previous ATTR-CM trials; however, CARDIO-TTRansform evaluated patients with a wide range of disease severity and receiving the contemporary standard of...

European journal of heart failure • 2026-10-28 • Phase III Randomized Trial
N = 130 88/100 PMID 42217207 ↗
Can This Approach Help? Inside the Latest Research on Switching from inotersen to eplontersen in patients with hereditary

Switching from inotersen to eplontersen further reduced serum TTR, halted disease progression, stabilized QoL, restored platelet count, and improved tolerability, without deterioration in nutritional status.

Journal of neurology • 2024-10-15 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 39138650 ↗
Can This Approach Help? Inside the Latest Research on Effect of Eplontersen on Cardiac Structure and Function in Patients With

Eplontersen was associated with stable or improved measures of cardiac structure and function vs historical placebo in patients with ATTRv polyneuropathy and cardiomyopathy.

Journal of cardiac failure • 2024-08-15 • Phase III Randomized Trial
N = 144 88/100 PMID 38065307 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Eplontersen Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI RXN-03109400-2689
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $0.2700/unit (~$8.10/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $47.63 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 17 Anonymous DotMD Community Micro-Logs $19.44 / mo View logs ↓
Hone Health Hormone & At-Home Biomarker Lab (Licensed Telehealth Cash Program) State-licensed clinician review • ~3d mail fulfillment $65.00 consult Program details
Midi Health Perimenopause & HRT Clinic (Licensed Telehealth Cash Program) State-licensed clinician review • ~2d mail fulfillment $59.00 consult Program details

Eplontersen Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Eplontersen RxNorm Concept ID RXN-03109400-2689 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $0.2700 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $47.63 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $19.44 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 83.00% Worth It (17 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Eplontersen Patient Community, Cohort Filters & Dosage Logs

Deterministic Eplontersen reference combining NIH RxNorm (RXN-03109400-2689), Medicaid NADAC ($0.2700/unit), and anonymous cohort outcomes (83% Worth It).

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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