Acute VTE in conjunction with VKA: (ASCO) + (NCCN) 50 kg: 5 mg once daily; 50–100 kg: 7.5 mg once daily; >100 kg: 10 mg once daily
2.5 mg
3.0 mg
Bioavailability (%)
100
100
100
Half-life ()
17 hours
60 days
60 days
Elimination
Renal
Renal
Renal
Antidote
None
None
Avidin
Market status/FDA approval
FDA approved for prevention and treatment of venous thromboembolism
In clinical trials
In clinical trials
Contraindication
(i) Patients with active bleeding (ii) Bacterial endocarditis (iii) Thrombocytopenia associated with positive antiplatelet antibodies
(i) Patients with CrCl <30 mL/min (ii) Neuraxial anesthesia (iii) Weight < 50 kg (prophylactic doses)
Not available
Not available
Monitoring parameters
Monitor hemoglobin, platelets
Not available
Not available
VTE: venous thromboembolism; VKA: vitamin K antagonist; ASCO: American Society of Clinical Oncology; NCCN: National Comprehensive Cancer Network; FDA: US Food and Drug Administration; CrCl: creatinine clearance.