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TNKase
The Fastest Lytic Delivery in AMI

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Deliver Just the Dose They Need


Single bolus TNKase features a simple, 5-tiered weight-based dosing schedule—tailored to the patient


Studies have shown that patient-optimized weight-based dosing, combined with single bolus administration, balances safety and efficacy1,2


TNKase is for IV administration only


The recommended total dose should not exceed 50 mg

  1. Murphy SA, Gibson CM, Van de Werf F, et al. Comparison of errors in estimating weight and in dosing of single bolus tenecteplase with tissue plasminogen activator (TIMI 10B and ASSENT 1). Am J Cardiol. 2002;90(1):51-54.


  2. Gibson CM, Marble SJ. Issues in the assessment of the safety and efficacy of tenecteplase (TNK-tPA). Clin Cardiol. 2001;24(9):577-584.


Indication: For use in mortality reduction associated with acute myocardial infarction (AMI). Treatment should be initiated as soon as possible after the onset of AMI symptoms.

Safety Information: TNKase therapy is contraindicated in the following conditions due to an increased risk of bleeding: active internal bleeding, history of cerebrovascular accident, intracranial or intraspinal surgery or trauma within 2 months, intracranial neoplasm, arteriovenous malformation, or aneurysm, known bleeding diathesis, and severe uncontrolled hypertension.

All thrombolytic agents increase the risk of bleeding, including intracranial bleeding, and should be used only in eligible patients. In addition, thrombolytic therapy increases the risk of stroke, including hemorrhagic stroke, particularly in elderly patients. In patients with large ST segment elevation myocardial infarction, physicians should choose either thrombolysis or percutaneous coronary intervention (PCI) as the primary treatment strategy for reperfusion. Rescue PCI or subsequent elective PCI may be performed after administration of thrombolytic therapies if medically appropriate.





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Please see TNKase full Prescribing Information. TNKaseTM (Tenecteplase). Activase® (Alteplase, recombinant).