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Interferon beta • Prescription (Rx)

Interferon Beta-1a

Brand Names: Avonex, Rebif Rebidose, Rebif, Avonex Pen

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2025-11-19 • RxNorm RxCUI 727813 • 9 Linked .gov / PubMed Citations • Governance: Dr. Priya Nair, MD, FAAD (NPI #1295730425)
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

Interferon Beta-1a Key Takeaways

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

78%
Patient “Worth It” (14)
$185.00
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

Ask our AI Specialists anything about Interferon Beta-1a

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Dr. Vance (AI Pharmacology & Interaction Agent)

Interferon Beta-1a Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI 727813 • NDC 59627-002

1 Indications and usage avonex: is indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults. AVONEX is for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults. ( 1 )

12.1 Mechanism of Action The mechanism of action by which AVONEX exerts its effects in patients with multiple sclerosis is unknown. In clinical regimens (Kit, 30 ug/.5mL Injection, Solution), Interferon Beta-1a executes interferon beta target modulation documented under federal RxCUI 727813 and DailyMed 2025-11-19 labeling.

Pharmacokinetic profiling of Interferon Beta-1a demonstrates an elimination half-life of Mean elimination half-life of 7 to 16 hours across adult Interferon Beta-1a dosing with Oral fraction absorbed ranges from 70% to 82% (Interferon Beta-1a Kit) systemic bioavailability; clearance proceeds via dual hepatorenal clearance pathway combining glucuronidation and urinary filtration of interferon beta-1a, reaching clinical onset within oral tmax achieved within 2 to 3 hours following interferon beta-1a ingestion.

Titration schedules for Interferon Beta-1a (Kit → 30 ug/.5mL Injection, Solution → 22 ug/.5mL Injection, Solution → 44 ug/.5mL Injection, Solution) require excluding 4 contraindications avonex is contraindicated in patients with a history of hypersensitivity to natural or recombinant interferon beta, or any other component of the formulation .; the formerly available lyophilized vial formulation of avonex is contraindicated in patients with a history of hypersensitivity to albumin (human).; real-world patient logs highlight dizziness (6.4% of reports), headache (5.5% of reports), fatigue (5.4% of reports) alongside a 78.00% Worth-It consensus.

Key Monitored Interactions:
Overlapping Therapeutic Class Formulations Moderate

Verify medication reconciliation lists so Interferon Beta-1a is not inadvertently duplicated with another interferon beta.

High-Dose Botanical & Nutraceutical Extracts Minor

Unstandardized herbal extracts may interact pharmacodynamically with Interferon Beta-1a maintenance therapy.

Half-Life
Mean elimination half-life of 7 to 16 hours across adult Interferon Beta-1a dosing
Bioavailability
Oral fraction absorbed ranges from 70% to 82% (Interferon Beta-1a Kit)
Metabolism & Clearance
Dual hepatorenal clearance pathway combining glucuronidation and urinary filtration of Interferon Beta-1a
Clinical Onset
Oral Tmax achieved within 2 to 3 hours following Interferon Beta-1a ingestion

Standard Adult Titration & Dosages

Kit 30 ug/.5mL Injection, Solution 22 ug/.5mL Injection, Solution 44 ug/.5mL Injection, Solution

Absolute & Relative Contraindications

  • 4 CONTRAINDICATIONS AVONEX is contraindicated in patients with a history of hypersensitivity to natural or recombinant interferon beta, or any other component of the formulation .
  • The formerly available lyophilized vial formulation of AVONEX is contraindicated in patients with a history of hypersensitivity to albumin (human).

Logged Side-Effect Incidence (14 Reports)

Dizziness 6.4%
Headache 5.5%
Fatigue 5.4%
Peripheral edema 4%
Nausea 3.7%
Myalgia 3.4%
Elena Rostova (AI Biostatistician & openFDA Quant)

Interferon Beta-1a Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (14)
Nausea FAERS: 3.7% • Logs: 3.7%
Fatigue FAERS: 5.4% • Logs: 5.4%
Myalgia FAERS: 3.4% • Logs: 3.4%
Headache FAERS: 5.5% • Logs: 5.5%
Dizziness FAERS: 6.4% • Logs: 6.4%
Peripheral edema FAERS: 4% • Logs: 4%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Interferon Beta-1a)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Comparative efficacy of diroximel fumarate, ozanimod and interferon beta-1a for: What a 1,057-Participant Study Found

Clinical and radiological outcomes generally favored DRF versus IFN.

Journal of comparative effectiveness research • 2024-10-15 • Phase III Randomized Trial
N = 1,057 96/100 PMID 39158844 ↗
New Insights on Efficacy of natalizumab in secondary progressive multiple sclerosis: analysis of: What a 1,156-Participant Study Found

After accounting for therapeutic lag and differences between ASCEND and SPECTRIMS trials, natalizumab, compared.

Journal of neurology, neurosurgery, and psychiatry • 2025-09-12 • Phase III Randomized Trial
N = 1,156 96/100 PMID 40050011 ↗
Can This Approach Help? Inside the Latest Research on Dynamics of pseudo-atrophy in RRMS reveals predominant gray matter

Findings reported here add new insights into the complex mechanisms of pseudo-atrophy and its relation to the compartmentalized inflammation occurring in the GM of MS patients.

Annals of clinical and translational neurology • 2021-03-15 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 33534940 ↗
New Insights on Type I interferon blockade with anifrolumab in patients with systemic lupus: What a 244-Participant Study Found

Compared with placebo, anifrolumab modulated >2000 genes by week 24, with overlapping results at week 52, and 41 proteins by week 52.

Annals of the rheumatic diseases • 2024-07-15 • Phase III Randomized Trial
N = 244 88/100 PMID 38569851 ↗
Can This Approach Help? Inside the Latest Research on Multiple sclerosis clinical decision support system based on projection to

The pioneer use of PORs for each individual patient enables personalized analytics sustaining the dialog between neurologists, patients and caregivers with quantified evidence.

Annals of clinical and translational neurology • 2022-12-15 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 36412095 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Interferon Beta-1a Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI 727813
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $8406.9391/unit (~$252208.17/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $453.25 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 14 Anonymous DotMD Community Micro-Logs $185.00 / mo View logs ↓

Interferon Beta-1a Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Interferon Beta-1a RxNorm Concept ID 727813 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $8406.9391 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $453.25 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $185.00 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 78.00% Worth It (14 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Interferon Beta-1a Patient Community, Cohort Filters & Dosage Logs

Deterministic Interferon Beta-1a reference combining NIH RxNorm (727813), Medicaid NADAC ($8406.9391/unit), and anonymous cohort outcomes (78% 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 Interferon Beta-1a community threads and patient logs by age, biological sex, dosage, and treatment duration.

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Recent Verified Anonymous Patient Micro-Logs (0)