Nebenwirkungen · Iclusig
Iclusig 15 mg film-coated tablets Iclusig 30 mg film-coated tablets Iclusig 45 mg film-coated tablets · Abschnitt 4.8 · PDF-Seite 17
HOS-128519 · Präparat HOS-096579
Arterial cardiovascular, cerebrovascular, and peripheral vascular occlusive adverse reactions (treatment-emergent frequencies) occurred in 13%, 9%, and 11% of Iclusig-treated patients, respectively. Overall arterial occlusive adverse reactions have occurred in 25% of Iclusig-treated patients from the PACE phase 2 trial with a minimum 64 months follow-up, with serious adverse reactions occurring in 20% of patients. Some patients experienced more than one type of event.
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Version 2026-07-31T14:12:00Z · SHA-256 4867aa10684948b4c421d8ab4cf806af86df3e9279763348c485fe3b6e3627c4 · Passage 6de922f4851d69f50a2063524f17bb146871887d3642d5b2e8349d71fe8bef72 · Zeichen 1133–1605 im Abschnitt