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van de patiënten in de fondaparinuxgroep ondervond 5,8% een bijwerking op of vóór dag 9 vergeleken met 5,7% van de met enoxaparine behandelde patiënten (risicoratio 1,01, 95% bi, 0,90; 1,13, eenzijdige non-inferieuriteits-p-waarde = mi
of the patients in the fondaparinux group, 5.8% experienced an event by day 9 compared to 5.7% for enoxaparin-treated patients (hazard ratio 1.01, du
Last Update: 2011-10-23
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