Difference between revisions of "Unfractionated heparin (UFH)"

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[[Category:Anticoagulants]]
 
[[Category:Anticoagulants]]
 
[[Category:Heparins]]
 
[[Category:Heparins]]
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[[Category:Venous thromboembolism (VTE) medications]]
  
 
[[Category:Drugs FDA approved in 1939]]
 
[[Category:Drugs FDA approved in 1939]]

Revision as of 02:29, 8 June 2018

General information

Class/mechanism: Acts at multiple points in the coagulation cascade to inhibit clotting and the formation of fibrin clots. Heparin interacts with antithrombin III (AT-III), inactivates the conversion of prothrombin to thrombin, inactivates thrombin and its effect of catalyzing the formation of fibrin from fibrinogen, and inhibits the activation of fibrin-stabilizing factor.[1][2][3]
Route: IV, SC
Extravasation: no information

For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]

Patient drug information

References