Reversal agent

Idarucizumab (Praxbind)

Also called Praxbind

Reviewed by Alex G, BSN, RN, CEN, CCRN, CMC, NREMT-P · From the Reference tab of the app

Indications

Dosing

WhereDose
Reversal and antidotesIdarucizumab (Praxbind): 5 g IV (two 2.5 g vials) for dabigatran

On the quick cards

Mechanism of action

Idarucizumab is a humanized monoclonal antibody fragment (Fab) that binds dabigatran and its active acylglucuronide metabolites, both free and bound to thrombin. It holds dabigatran about 350 times more tightly than dabigatran holds thrombin (Schiele 2013), binding 1:1 and essentially irreversibly, so thrombin is released and the anticoagulant effect disappears within minutes. Its binding pocket mimics thrombin's active site, but it binds no thrombin substrates and has no procoagulant or anticoagulant effect of its own.

Pharmacology

Pharmacokinetics

OnsetImmediate: unbound dabigatran below quantification after the dose (label)
DurationUsually lasting; clotting times rose again at 12–24 h in some as dabigatran returned from tissues (label)
Half-lifeInitial 47 min; terminal 10.3 h (label)
DistributionVd 8.9 L (label)
MetabolismProtein catabolism, mainly in the kidney (label)
Clearance47 mL/min (label)
EliminationGlomerular filtration, then tubular reabsorption and breakdown; 32% in urine within 6 h (label)
Organ failureExposure up 44% in mild and 84% in moderate kidney impairment; no dose change (label)
DialysisRemoves dabigatran (about 35% protein bound), a fallback when idarucizumab is unavailable

Chemistry

Adverse effects and cautions

In the one-pagers

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In the algorithms

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Sources

  1. FDA label: Praxbind (2023)
  2. Schiele 2013 (Blood)
  3. Pollack 2017 (RE-VERSE AD, NEJM)

For education and exam preparation only. Follow your institution’s protocols. Typical adult values for study. Follow the order, the label and your institution's protocols.