Bivalirudin
A hospital-administered anticoagulant used during cardiac procedures. Not a wellness peptide.
This peptide is an FDA-approved drug product that can be legally prescribed by licensed clinicians.
The basics
- Generic Name
- bivalirudin (peptide anticoagulant)
- Brand Names
- Angiomax
- Regulatory Status
- Prescribed by Doctors
- Therapeutic Areas
- Cardiovascular
- Prescribing Specialties
- Cardiology
What it does
Bivalirudin is an FDA-approved medication that your doctor can prescribe. Synthetic 20-amino acid peptide that directly and reversibly inhibits thrombin, preventing fibrin formation, platelet activation, and thrombus growth.
How it's taken
Intravenous infusion (hospital setting only)
How people access it
Hospital-administered during cardiac procedures. Not a take-home medication.
What doctors prescribe it for
- Anticoagulation during PCI
- Anticoagulation in patients with or at risk of heparin-induced thrombocytopenia (HIT) undergoing PCI
Clinicians may prescribe FDA-approved drugs for off-label uses based on their clinical judgment. Off-label indications have not undergone the same FDA review process as the labeled uses listed above.
How to know it's legit
You can independently verify the FDA-approval status of Bivalirudin through these free, publicly available databases:
- DailyMed (dailymed.nlm.nih.gov) — Search for Angiomax to find the current FDA-approved labeling, including indications, dosing, warnings, and contraindications.
- Drugs@FDA (accessdata.fda.gov/scripts/cder/daf/) — Search to find the original approval letter, review documents, and approval history.
- FDA Orange Book (orangebook.fda.gov) — Search for therapeutic equivalence evaluations and patent/exclusivity information.
Common Questions
Yes. Bivalirudin (Angiomax) is an FDA-approved drug product. It has undergone rigorous review of safety, efficacy, and manufacturing quality by the FDA. It can be legally prescribed by licensed clinicians for its approved indications.
Bivalirudin is FDA-approved for: Anticoagulation during PCI; Anticoagulation in patients with or at risk of heparin-induced thrombocytopenia (HIT) undergoing PCI. Off-label use may be considered by clinicians on a case-by-case basis, but only the labeled indications have been reviewed and approved by the FDA.
You can verify the approval status of Bivalirudin through several official FDA resources: DailyMed (dailymed.nlm.nih.gov) for current labeling, Drugs@FDA (accessdata.fda.gov/scripts/cder/daf/) for approval history, and the FDA Orange Book for therapeutic equivalence information. These are free, publicly available databases.
Want to learn more?
Explore how Bivalirudin compares to other options, or dive deeper into how FDA approval works.
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