Nebenwirkungen · NeoRecormon
NeoRecormon 500 IU solution for injection in pre-filled syringe NeoRecormon 2 000 IU solution for injection in pre-filled syringe NeoRecormon 3 000 IU solution for injection in pre-filled syringe NeoRecormon 4 000 IU solution for injection in pre-filled syringe NeoRecormon 5 000 IU solution for injection in pre-filled syringe NeoRecormon 6 000 IU solution for injection in pre-filled syringe NeoRecormon 10 000 IU solution for injection in pre-filled syringe NeoRecormon 20 000 IU solution for injection in pre-filled syringe NeoRecormon 30 000 IU solution for injection in pre-filled syringe · Abschnitt 4.8 · PDF-Seite 11
HOS-086032 · Präparat HOS-083248
Patients in an autologous blood pre-donation programme Patients in an autologous blood pre-donation programme have been reported to show a slightly higher frequency of thromboembolic events. However, a causal relationship with treatment with NeoRecormon could not be established.
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-02T10:00:00Z · SHA-256 d4885cc4a4f4b8eee4e66452aecdcfd9e0cb2d83ca77d038cff33e2a87f9cdac · Passage 6d6da3956c3749018f605f9182409c121e9bbcc6d993c2008eeb021f941ee8ac · Zeichen 2186–2465 im Abschnitt