Haj, M. A., Murch, N., Bowen, Derrick John, Sati, H. I., Beddal, A., Benton, A. and Collins, Peter William ORCID: https://orcid.org/0000-0002-6410-1324 2006. Cefotaxime as the potential cause of transient acquired von Willebrand syndrome. European Journal of Haematology 76 (5) , pp. 440-443. 10.1111/j.0902-4441.2006.t01-1-EJH2386.x |
Official URL: http://dx.doi.org/10.1111/j.0902-4441.2006.t01-1-E...
Abstract
Acquired von Willebrand syndrome (AvWS) is a relatively rare bleeding disorder. It has been reported in association with myeloproliferative disorders, autoimmune diseases, plasma cell dyscrasias and certain drugs. Cefotaxime is a third generation cephalosporin widely used for surgical prophylaxis and as empirical treatment of bacterial meningitis. We report a case of a transient AvWS in association with cefotaxime therapy.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Medicine Systems Immunity Research Institute (SIURI) |
Subjects: | R Medicine > R Medicine (General) |
Uncontrolled Keywords: | acquired; von Willebrand syndrome; cefotaxime |
Publisher: | Wiley-Blackwell |
ISSN: | 0902-4441 |
Last Modified: | 04 Jan 2023 02:13 |
URI: | https://orca.cardiff.ac.uk/id/eprint/57558 |
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