Monograph Details
|
|
Hematology
> Thromboembolic disorders
|
|
ARGATROBAN |
| Manufacturer |
|
GlaxoSmithKline Pharmaceuticals |
| Legal Classification |
|
Rx
|
| Pharmacological Class |
|
Anticoagulant (thrombin inhibitor). |
| Generic Name |
|
Argatroban 100mg/mL; soln for IV infusion after dilution. |
| Indications |
|
Prophylaxis and treatment of thrombosis in heparin-induced thrombocytopenia (HIT) or in those with or at risk of HIT undergoing percutaneous coronary intervention (PCI). |
| Children |
<18yrs: not recommended. |
| Adults |
|
≥18yrs: HIT: Discontinue heparin and obtain baseline aPTT. Initially 2micrograms/kg per minute by continuous IV infusion; check aPTT 2 hrs after starting; titrate to 1.5–3x baseline aPTT (max 100seconds); max 10micrograms/kg per minute. PCI: initially 25micrograms/kg per minute by IV infusion, and 350micrograms/kg bolus by large bore IV line over 3–5minutes; titrate based on activated clotting time (ACT) to therapeutic ACT of 300–450seconds. For both: hepatic impairment: reduce dose (see literature). |
| Contraindications |
|
Overt major bleeding. Concomitant other parenteral anticoagulants. |
| Precautions |
|
Increased bleeding risk (eg, unexpected decreases in hematocrit or BP, severe hypertension, recent lumbar puncture, spinal anesthesia, major surgery, bleeding disorders, GI lesions). Pregnancy (Cat.B). Nursing mothers: not recommended. |
| Interactions |
|
Increased risk of bleeding with thrombolytics (eg, t-PA, streptokinase), Vit. K antagonists (eg, warfarin), heparin, antiplatelets, GP IIb/IIIa blockers (eg, eptifibatide). |
| Adverse Reactions |
|
Hemorrhagic events, chest pain, dyspnea, cough, hypotension, rash, fever, GI upset, cardiac arrest, ventricular tachycardia, others. |
| How Supplied |
|
Single-use vial (2.5mL)—1 |
|
|
|
|