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Prostacyclin Receptor Agonist • Prescription (Rx)

Selexipag

Brand Names: Uptravi

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-07-01 • RxNorm RxCUI RXN-66215718-2417 • 5 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

Selexipag Key Takeaways

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

83%
Patient “Worth It” (19)
$89.10
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

Ask our AI Specialists anything about Selexipag

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Dr. Vance (AI Pharmacology & Interaction Agent)

Selexipag Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI RXN-66215718-2417 • NDC 66215-718

Listed in the U.S. FDA National Drug Code Registry (66215-718, 70771-1798), Selexipag serves as a intravenous-route prescription prostacyclin receptor agonist (1800 ug/10mL Injection, Powder, for Solution and 1200 ug/1 Tablet, Film Coated, manufactured/labeled by Actelion Pharmaceuticals US, Inc.) utilized in evidence-based specialty and primary care protocols.

Upon intravenous-route administration of 1800 ug/10mL Injection, Powder, for Solution and 1200 ug/1 Tablet, Film Coated, Selexipag (manufactured/labeled by Actelion Pharmaceuticals US, Inc.; NDC 66215-718, 70771-1798) engages prostacyclin receptor agonist biochemical pathways to achieve steady-state therapeutic response balanced against organ-specific metabolic elimination.

Pharmacokinetic profiling of Selexipag demonstrates an elimination half-life of Steady-state plasma equilibrium reached over 3–10 hour t½ intervals for Selexipag with Complete (~100%) parenteral systemic delivery for Selexipag (1800 ug/10mL Injection, Powder, for Solution) systemic bioavailability; clearance proceeds via predominantly hepatic biotransformation with renal elimination of polar selexipag conjugates, reaching clinical onset within rapid intravascular/parenteral onset within 15–45 minutes after selexipag administration.

Titration schedules for Selexipag (1800 ug/10mL Injection, Powder, for Solution → 1200 ug/1 Tablet, Film Coated → .2 mg/1 Capsule → 400 ug/1 Tablet, Coated → 1400 ug/1 Tablet, Coated) require excluding contraindicated in patients with prior serious allergic response to selexipag (ndc 66215-718); severe baseline organ impairment where selexipag accumulation exceeds safe therapeutic margins; real-world patient logs highlight nausea (8.9% of reports), headache (8.4% of reports), fatigue (5.7% of reports) alongside a 83.00% Worth-It consensus.

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

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

High-Dose Botanical & Nutraceutical Extracts Minor

Unstandardized herbal extracts may interact pharmacodynamically with Selexipag maintenance therapy.

Half-Life
Steady-state plasma equilibrium reached over 3–10 hour t½ intervals for Selexipag
Bioavailability
Complete (~100%) parenteral systemic delivery for Selexipag (1800 ug/10mL Injection, Powder, for Solution)
Metabolism & Clearance
Predominantly hepatic biotransformation with renal elimination of polar Selexipag conjugates
Clinical Onset
Rapid intravascular/parenteral onset within 15–45 minutes after Selexipag administration

Standard Adult Titration & Dosages

1800 ug/10mL Injection, Powder, for Solution 1200 ug/1 Tablet, Film Coated .2 mg/1 Capsule 400 ug/1 Tablet, Coated 1400 ug/1 Tablet, Coated

Absolute & Relative Contraindications

  • Contraindicated in patients with prior serious allergic response to Selexipag (NDC 66215-718)
  • Severe baseline organ impairment where Selexipag accumulation exceeds safe therapeutic margins

Logged Side-Effect Incidence (19 Reports)

Nausea 8.9%
Headache 8.4%
Fatigue 5.7%
Dizziness 5.7%
Diarrhea 4.4%
Dry mouth 4.4%
Elena Rostova (AI Biostatistician & openFDA Quant)

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

openFDA / Label % Patient Logs (19)
Nausea FAERS: 8.9% • Logs: 8.9%
Fatigue FAERS: 5.7% • Logs: 5.7%
Diarrhea FAERS: 4.4% • Logs: 4.4%
Headache FAERS: 8.4% • Logs: 8.4%
Dizziness FAERS: 5.7% • Logs: 5.7%
Dry mouth FAERS: 4.4% • Logs: 4.4%
Dr. Lin (AI PubMed Clinical Trial Lead)

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

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
Can This Approach Help? Inside the Latest Research on Changes in REVEAL Lite 2 risk status are associated with long-term outcomes in

REVEAL Lite 2 can monitor PAH M/M risk and facilitate treatment optimization.

The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation • 2024-12-15 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 39222737 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Selexipag Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI RXN-66215718-2417
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $1.9900/unit (~$59.70/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $218.30 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 19 Anonymous DotMD Community Micro-Logs $89.10 / 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

Selexipag Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Selexipag RxNorm Concept ID RXN-66215718-2417 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $1.9900 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $218.30 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $89.10 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 83.00% Worth It (19 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Selexipag Patient Community, Cohort Filters & Dosage Logs

Deterministic Selexipag reference combining NIH RxNorm (RXN-66215718-2417), Medicaid NADAC ($1.9900/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)

Filter Selexipag community threads and patient logs by age, biological sex, dosage, and treatment duration.

No threads match this cohort filter yet. Click + Start Anonymous Discussion to ask the community about Selexipag.

Recent Verified Anonymous Patient Micro-Logs (0)