Dabigatran: Difference between revisions

(Redirected page to Dabigatran (Pradaxa) reversal)
(Created Dabigatran medication page with dosing (replacing redirect to Dabigatran reversal); added SMW Indications by Condition query)
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#REDIRECT[[Dabigatran (Pradaxa) reversal]]
==Administration==
*Type: [[Anticoagulant]], Direct Thrombin Inhibitor
*Dosage Forms: capsule
*Dosage Strengths: 75mg, 110mg, 150mg
*Routes of Administration: Oral
*Common Trade Names: Pradaxa
 
==Adult Dosing==
===Stroke prevention in [[atrial fibrillation]] (nonvalvular)===
*150mg PO BID (CrCl >30)
*75mg PO BID (CrCl 15-30)
 
===[[DVT]]/[[PE]] Treatment===
*150mg PO BID after 5-10 days of parenteral anticoagulation
 
===[[DVT]]/[[PE]] Prophylaxis (post hip replacement)===
*110mg PO on day of surgery (1-4h post-op), then 220mg PO QD x28-35 days
 
==Pediatric Dosing==
''Safety/efficacy not established''
 
==Special Populations==
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: C
*[[Lactation risk categories|Lactation risk]]: Infant risk cannot be ruled out
*Renal dosing:
**Afib: 75mg BID if CrCl 15-30; avoid if CrCl <15
**DVT/PE treatment: avoid if CrCl <30
*Hepatic dosing: No adjustment required; avoid in severe impairment
*Decrease dose if concomitant use of P-gp inhibitors (e.g., dronedarone, systemic ketoconazole) with CrCl 30-50
 
==Contraindications==
*Allergy to class/drug
*Active pathological bleeding
*Mechanical prosthetic heart valve
*CrCl <30 (DVT/PE treatment)
*Concomitant use of P-gp inhibitors with CrCl <30
 
==Adverse Reactions==
===Serious===
*[[Anticoagulant reversal for life-threatening bleeds|Bleeding, severe]]
**[[Idarucizumab]] (Praxbind): specific reversal agent
*Epidural/[[spinal hematoma]]
*GI hemorrhage
 
===Common===
*Dyspepsia, GI discomfort (most common reason for discontinuation)
*Easy bruising, epistaxis
 
==Pharmacology==
*Half-life: 12-17 hours (prolonged with renal impairment)
*Metabolism: Conjugation (not CYP450 dependent)
*Excretion: 80% renal
*Bioavailability: 3-7% (capsules must not be crushed or opened)
 
==Mechanism of Action==
*Direct, competitive, reversible inhibitor of free and clot-bound thrombin (factor IIa)
 
==Comments==
*Only NOAC with a specific reversal agent: [[Idarucizumab]] (Praxbind) 5g IV
*Must be stored in original packaging (sensitive to moisture)
*Cannot be crushed, chewed, or placed in feeding tubes (bioavailability changes dramatically)
*Higher rate of GI bleeding compared to warfarin; lower rate of intracranial hemorrhage
*aPTT provides qualitative assessment of anticoagulant effect; Thrombin Time (TT) is most sensitive — normal TT excludes significant drug effect
*Dialyzable (~60% removed over 2-3h)
 
==Indications by Condition==
''The following table is automatically generated from disease/condition pages across WikEM.''
{{#ask:[[Has DrugName::Dabigatran]]
|?Has Indication=Indication
|?Has Dose=Dose
|?Has Context=Context
|?Has Route=Route
|?Has Population=Population
|format=table
|headers=plain
|mainlabel=-
|sort=Has Indication
|limit=50
}}
 
==See Also==
*[[Dabigatran reversal]]
*[[Idarucizumab]]
*[[Anticoagulant reversal for life-threatening bleeds]]
*[[Procedures in patients with coagulopathies]]
*[[Atrial fibrillation (main)]]
 
==References==
<references/>
 
[[Category:Pharmacology]]

Latest revision as of 01:10, 25 March 2026

Administration

  • Type: Anticoagulant, Direct Thrombin Inhibitor
  • Dosage Forms: capsule
  • Dosage Strengths: 75mg, 110mg, 150mg
  • Routes of Administration: Oral
  • Common Trade Names: Pradaxa

Adult Dosing

Stroke prevention in atrial fibrillation (nonvalvular)

  • 150mg PO BID (CrCl >30)
  • 75mg PO BID (CrCl 15-30)

DVT/PE Treatment

  • 150mg PO BID after 5-10 days of parenteral anticoagulation

DVT/PE Prophylaxis (post hip replacement)

  • 110mg PO on day of surgery (1-4h post-op), then 220mg PO QD x28-35 days

Pediatric Dosing

Safety/efficacy not established

Special Populations

  • Pregnancy Rating: C
  • Lactation risk: Infant risk cannot be ruled out
  • Renal dosing:
    • Afib: 75mg BID if CrCl 15-30; avoid if CrCl <15
    • DVT/PE treatment: avoid if CrCl <30
  • Hepatic dosing: No adjustment required; avoid in severe impairment
  • Decrease dose if concomitant use of P-gp inhibitors (e.g., dronedarone, systemic ketoconazole) with CrCl 30-50

Contraindications

  • Allergy to class/drug
  • Active pathological bleeding
  • Mechanical prosthetic heart valve
  • CrCl <30 (DVT/PE treatment)
  • Concomitant use of P-gp inhibitors with CrCl <30

Adverse Reactions

Serious

Common

  • Dyspepsia, GI discomfort (most common reason for discontinuation)
  • Easy bruising, epistaxis

Pharmacology

  • Half-life: 12-17 hours (prolonged with renal impairment)
  • Metabolism: Conjugation (not CYP450 dependent)
  • Excretion: 80% renal
  • Bioavailability: 3-7% (capsules must not be crushed or opened)

Mechanism of Action

  • Direct, competitive, reversible inhibitor of free and clot-bound thrombin (factor IIa)

Comments

  • Only NOAC with a specific reversal agent: Idarucizumab (Praxbind) 5g IV
  • Must be stored in original packaging (sensitive to moisture)
  • Cannot be crushed, chewed, or placed in feeding tubes (bioavailability changes dramatically)
  • Higher rate of GI bleeding compared to warfarin; lower rate of intracranial hemorrhage
  • aPTT provides qualitative assessment of anticoagulant effect; Thrombin Time (TT) is most sensitive — normal TT excludes significant drug effect
  • Dialyzable (~60% removed over 2-3h)

Indications by Condition

The following table is automatically generated from disease/condition pages across WikEM.

IndicationDoseContextRoutePopulation
Atrial fibrillation (main)150 mg BID (reduced: 75 mg BID if CrCl 15-30)Anticoagulation (NOAC)POAdult

See Also

References