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TNKase
The Fastest Lytic Delivery in AMI

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We hope that TNKase.com has provided useful information about the only FDA approved single bolus thrombolytic agent for the treatment of acute myocardial infarction (AMI). We encourage you to share this site with a colleague: Simply provide the information specified below and click the Submit button, and your colleague will receive an e-mail message containing a link to TNKase.com.

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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).