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Acute agranulocytosis after oral administration of dabigatran: a rare case report and a short review of literature
Authors:Sergio Fasullo  Stefania Davì  Gioacchino Cosenza  Francesca Di Franco  Nicola La Manna  Alfonso Giubilato  Graziella Vetrano  Giorgio Maringhini
Affiliation:1.Coronary Care Unit, “O.Barberi”, “G.F.Ingrassia” Hospital,Palermo,Italy;2.Chemistry and Pharmaceutical Technologies,Palermo,Italy;3.Department Cardiology “Paolo Borsellino”,“G.F.Ingrassia” Hospital,Palermo,Italy
Abstract:
This case report describes agranulocytosis immediately after oral administration of dabigatran in a 68 years old man with atrial fibrillation (AF). Dabigatran is an oral, reversible and competitive thrombin inhibitor that has shown promising results. In patients with atrial fibrillation of RE-LY study (Randomized Evaluation of Long-Term Anticoagulant Therapy), dabigatran administered at a dose of 150 mg, as compared with warfarin, was associated with lower rates of stroke and systemic embolism but similar rates of major hemorrhage. Dabigatran is administered as a prodrug and the peak of the plasma concentrations occurs within 2 h of ingestion. Agranulocytosis is characterized by a severe decrease or lack of circulating granulocytes. This rare event can be found among people taking dabigratan, especially for people who are female, over the age of 60, who took the drug for
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