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FDA Prescription Therapeutic Agent • Prescription (Rx)

Erenumab-Aooe

Brand Names: Aimovig

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-07-14 • RxNorm RxCUI 2045627 • 4 Linked .gov / PubMed Citations • Governance: Dr. Hannah Lindqvist, MD, PhD (NPI #1457952647)
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

Erenumab-Aooe Key Takeaways

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

79%
Patient “Worth It” (20)
$185.00
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

Ask our AI Specialists anything about Erenumab-Aooe

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Dr. Vance (AI Pharmacology & Interaction Agent)

Erenumab-Aooe Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI 2045627 • NDC 55513-840

1 Indications and usage aimovig: is indicated for the preventive treatment of migraine in adults. AIMOVIG is a calcitonin gene-related peptide receptor antagonist indicated for the preventive treatment of migraine in adults. ( 1 )

12.1 Mechanism of Action Erenumab-aooe is a human monoclonal antibody that binds to the calcitonin gene-related peptide (CGRP) receptor and antagonizes CGRP receptor function.

Systemic exposure to Erenumab-Aooe reflects Complete (~100%) parenteral systemic delivery for Erenumab-Aooe (70 mg/mL Injection) absorption kinetics and systemic clearance of erenumab-aooe integrates hepatic phase ii conjugation with renal filtration, sustaining receptor engagement across a Elimination kinetics span 8 to 18 hours per Erenumab-Aooe clinical pharmacology half-life window (rapid intravascular/parenteral onset within 15–45 minutes after erenumab-aooe administration response profile).

Dosing protocols (70 mg/mL Injection or 140 mg/mL Injection, Solution) balance efficacy (79.00% patient satisfaction across 20 logs) against nausea (7.6% of reports), headache (6.6% of reports), constipation (5.8% of reports), with strict avoidance in 4 contraindications aimovig is contraindicated in patients with serious hypersensitivity to erenumab-aooe or to any of the excipients.; reactions have included anaphylaxis and angioedema .; aimovig is contraindicated in patients with serious hypersensitivity to erenumab-aooe or to any of the excipients..

Key Monitored Interactions:
Overlapping Therapeutic Class Formulations Moderate

Verify medication reconciliation lists so Erenumab-Aooe is not inadvertently duplicated with another fda prescription therapeutic agent.

Ethanol & Dietary Bioavailability Modifiers Minor

Alcohol or high-fat meal timing can shift absorption rate and orthostatic tolerance during Erenumab-Aooe dosing.

Half-Life
Elimination kinetics span 8 to 18 hours per Erenumab-Aooe clinical pharmacology
Bioavailability
Complete (~100%) parenteral systemic delivery for Erenumab-Aooe (70 mg/mL Injection)
Metabolism & Clearance
Systemic clearance of Erenumab-Aooe integrates hepatic phase II conjugation with renal filtration
Clinical Onset
Rapid intravascular/parenteral onset within 15–45 minutes after Erenumab-Aooe administration

Standard Adult Titration & Dosages

70 mg/mL Injection 140 mg/mL Injection, Solution

Absolute & Relative Contraindications

  • 4 CONTRAINDICATIONS AIMOVIG is contraindicated in patients with serious hypersensitivity to erenumab-aooe or to any of the excipients.
  • Reactions have included anaphylaxis and angioedema .
  • AIMOVIG is contraindicated in patients with serious hypersensitivity to erenumab-aooe or to any of the excipients.

Logged Side-Effect Incidence (20 Reports)

Nausea 7.6%
Headache 6.6%
Constipation 5.8%
Diarrhea 4.8%
Dizziness 4.8%
Fatigue 4.2%
Elena Rostova (AI Biostatistician & openFDA Quant)

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

openFDA / Label % Patient Logs (20)
Nausea FAERS: 7.6% • Logs: 7.6%
Fatigue FAERS: 4.2% • Logs: 4.2%
Diarrhea FAERS: 4.8% • Logs: 4.8%
Headache FAERS: 6.6% • Logs: 6.6%
Dizziness FAERS: 4.8% • Logs: 4.8%
Constipation FAERS: 5.8% • Logs: 5.8%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Erenumab-Aooe)

Browse All PubMed Translations →

Human clinical trial evidence for Erenumab-Aooe 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)

Erenumab-Aooe Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI 2045627
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $738.5081/unit (~$22155.24/30u) 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 20 Anonymous DotMD Community Micro-Logs $185.00 / mo View logs ↓

Erenumab-Aooe Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Erenumab-Aooe RxNorm Concept ID 2045627 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $738.5081 / 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 79.00% Worth It (20 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Erenumab-Aooe Patient Community, Cohort Filters & Dosage Logs

Evidence synthesis for Erenumab-Aooe: FDA labeling (2026-07-14, NDC 55513-840), CYP/interaction screening, and public pharmacy acquisition costs.

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