Interaction between the LMWH reviparin and aspirin in healthy volunteers

Aims To investigate potential interactions between reviparin and acetylsalicylic acid (ASA 300 mg o.d. from day 1–5). Methods In an open, randomized, three‐way‐cross over study nine healthy volunteers received reviparin (s.c. injection of 6300 anti‐Xa units) or placebo from days 3 to 5 and acetylsal...

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Published inBritish journal of clinical pharmacology Vol. 49; no. 4; pp. 337 - 341
Main Authors Klinkhardt, Ute, Breddin, Hans Klaus, Esslinger, Heinz Ulrich, Haas, Silvia, Kalatzis, Andreas, Harder, Sebastian
Format Journal Article Conference Proceeding
LanguageEnglish
Published Oxford, UK Blackwell Science Ltd 01.04.2000
Blackwell Science
Blackwell Science Inc
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ISSN0306-5251
1365-2125
DOI10.1046/j.1365-2125.2000.00173.x

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Summary:Aims To investigate potential interactions between reviparin and acetylsalicylic acid (ASA 300 mg o.d. from day 1–5). Methods In an open, randomized, three‐way‐cross over study nine healthy volunteers received reviparin (s.c. injection of 6300 anti‐Xa units) or placebo from days 3 to 5 and acetylsalicylic acid (ASA 300 mg) or placebo from days 1 to 5. Assessments included bleeding time (BT), collagen (1 µg ml−1) induced platelet aggregation (CAG), heptest, plasma antifactor Xa‐activity and activated partial thromboplastin time (aPTT). Results Median bleeding time at day 5 was 5.5 min after reverparin alone and after ASA alone and was 9.6 min after the combination of reviparin and ASA. ASA treatment reduced CAG from 84% to 40 to 50% of Amax; values after combined treatment of reviparin with ASA were not different from those after ASA alone. aPTT was prolonged to 32 s after reviparin; this effect was not modified if subjects received ASA. Combined treatment with ASA and reviparin had no effect on plasma anti‐Xa‐activity and heptest compared with reviparin alone. Conclusions We could not entirely exclude a small interaction between reviparin and ASA on bleeding time, but the effect is probably without clinical significance.
Bibliography:Received 30 March 1999, accepted 4 January 2000.
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ISSN:0306-5251
1365-2125
DOI:10.1046/j.1365-2125.2000.00173.x