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v ključnem kliničnem preskušanju ua/ nstemi, zdravljenja s fondaparinuksom niso uvedli prej kot 2 uri po
in the pivotal ua/ nstemi clinical trial, treatment with fondaparinux was restarted no earlier than 2 hours after sheath removal.
v študiji iii. faze ua/ nstemi so najpogosteje poročali o naslednjih neželenih učinkih, ki niso bili
4.1% (enoxaparin) up to and including day 9 in the phase iii ua/ nstemi study, and the incidence of adjudicated severe hemorrhage by modified timi criteria was 1.1% (fondaparinux) vs.
preprečevanje vte in zdravljenje ua/nstemi in stemi - bolniki s telesno maso < 50 kg imajo povečano tveganje za krvavitev.
prevention of vte and treatment of ua/nstemi and stemi - patients with body weight <50 kg are at increased risk of bleeding.