Nebenwirkungen · Alprolix
ALPROLIX 250 IU powder and solvent for solution for injection ALPROLIX 500 IU powder and solvent for solution for injection ALPROLIX 1000 IU powder and solvent for solution for injection ALPROLIX 2000 IU powder and solvent for solution for injection ALPROLIX 3000 IU powder and solvent for solution for injection · Abschnitt 4.8 · PDF-Seite 7
HOS-135649 · Präparat HOS-097754
Previously Untreated Patients (PUPs): A total of 33 patients with severe haemophilia B were observed in one clinical study. Adverse events were monitored for a total of 57.51 subject-years. The total number of exposure days was 2,233 with a median of 76 (range 1 to 137) exposure days per subject.
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Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2026-07-06T02:00:00Z · SHA-256 e42dd716e190b5b1801370fcbf09f24ba5358dc15bf28247721be9dcc9a1d1b1 · Passage 5e5baecee15dd6747f995b40d343c11d95b6f9c784e63f5696c2a4daecc20585 · Zeichen 1889–2186 im Abschnitt