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Drugs reference index «Bivalirudin»


Pronunciation: (bye-VAL-ih-ruh-din)Class: Thrombin inhibitor

Trade Names:Angiomax- Powder for injection, lyophilized 250 mg


Inhibits thrombin by reversibly binding to the catalytic site and the anion-binding exosite of circulating and clot-bound thrombin.



Steady-state concentration is about 12.3 mcg/mL.


Not bound to plasma proteins (other than thrombin) or red blood cells.


Cleared from plasma by renal mechanisms and proteolytic cleavage; elimination related to glomerular filtration rate. The t ½ is 25 min. Cl is 3.4 mL/min/kg.


Produces immediate anticoagulant effect.


Coagulation times return to baseline about 1 h following end of administration.

Special Populations

Renal Function Impairment

Cl is reduced about 20% in moderate to severe renal function impairment and about 80% in dialysis-dependent patients.

Indications and Usage

Anticoagulant in combination with aspirin in patients with unstable angina undergoing percutaneous transluminal coronary angioplasty (PTCA); anticoagulant in combination with aspirin and provisional use of glycoprotein IIb/IIIa (GPIIb/IIIa) inhibitor in patients undergoing percutaneous coronary intervention (PCI); in combination with aspirin for treatment of patients with, or at risk of heparin-induced thrombocytopenia or heparin-induced thrombocytopenia and thrombosis syndrome (HIT/HITTS) undergoing PCI.


Active major bleeding, hypersensitivity to bivalirudin.

Dosage and Administration


IV Bolus dose of 0.75 mg/kg followed by an infusion of 1.75 mg/kg/h for duration of PCI procedure. Five minutes after bolus dose, obtain ACT and administer additional bolus of 0.3 mg/kg if indicated.


IV Bolus dose of 0.75 mg/kg, followed by a continuous infusion at a rate of 1.75 mg/kg/h for the duration of the procedure.

Continuation of TherapyAdults

IV Infusion may be continued for up to 4 h post-procedure as indicated. After 4 h, an additional IV infusion of 0.2 mg/kg/h for up to 20 h may be given if needed.

Concomitant TherapyAdults

PO Bivalirudin is intended for concurrent use with aspirin (300 to 325 mg/day).

Renal Function ImpairmentAdults

IV Ccr 30 to 50 mL/min: Administer infusion at rate of 1.75 mg/kg/h. Ccr less than 30 mL/min: Reduce infusion rate to 1 mg/kg/h. Hemodialysis: Reduce infusion rate to 0.25 mg/kg/h. No reduction in bolus dose needed.

General Advice

  • For IV administration only. Not for intradermal, subcutaneous, IM, or intra-arterial administration.
  • Reconstitute powder for injection with 5 mL sterile water for injection. Gently swirl until powder is dissolved.
  • For initial bolus infusion, further dilute each reconstituted via in 50 mL of 5% dextrose in water or sodium chloride 0.9% for injection to yield a final concentration of 5 mg/mL.
  • For low rate infusion, further dilute each reconstituted vial in 500 mL of 5% dextrose in water or sodium chloride 0.9% for injection to yield a final concentration of 0.5 mg/mL.
  • Do not mix with the following drugs in the same IV line: alteplase, amiodarone, amphotericin B, chlorpromazine, diazepam, dobutamine, prochlorperazine, reteplase, streptokinase, vancomycin.
  • Reconstituted bivalirudin should be a clear to slightly opalescent, colorless to slightly yellow solution. Do not administer if reconstituted or diluted solution is discolored, cloudy, or contains particulate matter.
  • Maintain meticulous catheter technique, with frequent aspiration and flushing, paying special attention to minimizing conditions of stasis within the catheter or vessels.
  • Discard any unused reconstituted or diluted solution.


Store unopened vials at controlled room temperature (59° to 86°F). Refrigerate reconstituted solution up to 24 h (36° to 46°F). Diluted solution may be stored for up to 24 h at controlled room temperature. Protect reconstituted solutions from freezing.

Drug Interactions

Glycoprotein IIb/IIIa inhibitors, heparin, thrombolytics, warfarin

The risk of major bleeding may be increased.

Laboratory Test Interactions

None well documented.

Adverse Reactions


Hypotension (12%); hypertension (6%); bradycardia (5%); thrombus formation during PCI with and without intracoronary brachytherapy (postmarketing).


Headache (12%); insomnia (7%); anxiety (6%); nervousness (5%).


Nausea (15%); vomiting (6%); abdominal pain, dyspepsia (5%).


Urinary retention (4%).


Major hemorrhage (4%); fatal bleeding (postmarketing).


Back pain (42%); pain (15%); injection site pain (8%); pelvic pain (6%); fever (5%); hypersensitivity and allergic reactions including rare reports of anaphylaxis (postmarketing).



Monitor patient for signs of bleeding throughout therapy.


Category B .




Safety and efficacy not established.


More bleeding events reported in elderly patients than younger patients.

Special Risk Patients

Use with caution in patients with disease states associated with an increased risk of bleeding.


Use with caution; increased risk of thrombus formation has been associated with use of bivalirudin as the antithrombin in gamma brachytherapy.


May occur at any site. Avoid IM injections of other medications. Venipuncture sites may require pressure to prevent bleeding and hematoma formation. Consider hemorrhagic event if unexplained fall in hematocrit or BP, or any unexplained symptom is noted.


Treatment-emergent positive antibody tests may occur.



Adverse reactions have not been reported; however, monitor for signs of bleeding.

Patient Information

  • Advise patient that medication will be prepared and administered by health care provider before PTCA is attempted and for several hours after the procedure.
  • Instruct patient to inform health care provider if any of the following symptoms are noted during the administration of drug: back pain, bleeding, headache, nausea, pain, pain at the injection site.

Copyright © 2009 Wolters Kluwer Health.

  • Bivalirudin MedFacts Consumer Leaflet (Wolters Kluwer)
  • bivalirudin Concise Consumer Information (Cerner Multum)
  • bivalirudin Intravenous Advanced Consumer (Micromedex) - Includes Dosage Information
  • Angiomax Prescribing Information (FDA)