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Erschienen in: Drugs 12/2008

01.08.2008 | Adis Drug Profile

Dabigatran Etexilate

verfasst von: Mark Sanford, Greg L. Plosker

Erschienen in: Drugs | Ausgabe 12/2008

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Abstract

  • ▲ Dabigatran etexilate is an orally administered prodrug of dabigatran, which is a potent, concentration-dependent inhibitor of thrombus formation and thrombin-induced platelet aggregation.
  • ▲ Dabigatran etexilate pharmacokinetics were linear across a wide dosage range. There were no clinically important pharmacokinetic interactions with digoxin (a P-glycoprotein substrate), pantoprazole (a proton-pump inhibitor) or drugs that are substrates and/or inhibitors of hepatic cytochrome P450 enzymes.
  • ▲ In two large, randomized, double-blind trials of the prevention of venous thromboembolism (VTE) in patients undergoing total hip or total knee replacement surgery, orally administered dabigatran etexilate 220 mg/day was noninferior to subcutaneous enoxaparin sodium 40 mg/day for the primary composite endpoint of total VTE events or all-cause mortality during the treatment period.
  • ▲ There were no significant differences between dabigatran etexilate and enoxaparin sodium in major VTE events and VTE-related mortality. Across trials, ≤0.5% of patients experienced a symptomatic pulmonary embolus or died.
  • ▲ Dabigatran etexilate was generally well tolerated. In patients undergoing total hip or total knee replacement surgery, there was no significant difference between dabigatran etexilate and enoxaparin sodium recipients in the incidence of major or minor bleeding.
Fußnoten
1
The use of trade names is for identification purposes only and does not imply endorsement.
 
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Metadaten
Titel
Dabigatran Etexilate
verfasst von
Mark Sanford
Greg L. Plosker
Publikationsdatum
01.08.2008
Verlag
Springer International Publishing
Erschienen in
Drugs / Ausgabe 12/2008
Print ISSN: 0012-6667
Elektronische ISSN: 1179-1950
DOI
https://doi.org/10.2165/00003495-200868120-00007

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