Nebenwirkungen · Arixtra
Arixtra 10 mg/0.8 ml solution for injection, pre-filled syringe. · Abschnitt 4.8 · PDF-Seite 58–59
HOS-110209 · Präparat HOS-093307
58 In addition, 8 patients (2.2%) had overt bleeding for which a blood product was administered, and which was not directly attributable to the patient’s underlying medical condition and 4 patients (1.1%) had bleeding that required medical or surgical intervention. All these events warranted either interruption or withdrawal of fondaparinux treatment except for 1 patient for whom the action taken with fondaparinux was not reported. An additional 65 patients (17.8%) reported other overt bleeding events or menstrual bleeding resulting in a medical consultation and/or intervention.
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Version 2026-05-07T11:30:00Z · SHA-256 381af76ffd2bbb8fff8013d6d98ed50ab7a9f4fb8da38de9af66e45dcfd01fac · Passage 5ae9084a1203a750d2e19939a8d83052e8536c20b005c7f685823b9d10fa1d02 · Zeichen 6511–7097 im Abschnitt