⚠ LIVE — European Consumer Safety Watch 💊 Etichetă canal medical: 18 în ultimele 7 zile 🍎 Canal alimentar: 180 în ultimele 7 zile 🧸 Produse canal: 48 în ultimele 7 zile 🟢 Monitorizare: EMA · RASFF · NVWA · FAGG · FAVV · EFSA · Safety Gate ⏱ Ultima preluare: 1 minut în urmă ⚠ LIVE — European Consumer Safety Watch 💊 Etichetă canal medical: 18 în ultimele 7 zile 🍎 Canal alimentar: 180 în ultimele 7 zile 🧸 Produse canal: 48 în ultimele 7 zile 🟢 Monitorizare: EMA · RASFF · NVWA · FAGG · FAVV · EFSA · Safety Gate ⏱ Ultima preluare: 1 minut în urmă
🛡️ EUSW
🇷🇴
💊

Usgena

ustekinumab
Boala Crohn;Psoriazis;Artrită psoriazică;Colită ulcerativă
✅ Autorizat Biosimilar
Nu există alerte active
Acest medicament nu are penurii în curs, scrisori de siguranță sau retrageri de pe piață.

La ce se utilizează

Crohn’s Disease Usgena is indicated for the treatment of adult patients with moderately to severely active Crohn’s disease who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a TNFα antagonist. Ulcerative colitis Usgena is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic. Plaque psoriasis Usgena is indicated for the treatment of moderate to severe plaque psoriasis in adults who failed to respond to, or who have a contraindication to, or are intolerant to other systemic therapies including ciclosporin, methotrexate (MTX) or PUVA (psoralen and ultraviolet A) (see section 5.1). Paediatric plaque psoriasis Usgena is indicated for the treatment of moderate to severe plaque psoriasis in children and adolescent patients from the age of 6 years and older, who are inadequately controlled by, or are intolerant to, other systemic therapies or phototherapies (see section 5.1). Psoriatic arthritis (PsA) Usgena, alone or in combination with MTX, is indicated for the treatment of active psoriatic arthritis in adult patients when the response to previous non-biological disease-modifying anti-rheumatic drug (DMARD) therapy has been inadequate (see section 5.1).

⚠️ Siguranță a pacientului

No

⚠️ Agregăm anunțuri oficiale. Nu oferim sfaturi medicale. Pentru decizii medicale sau juridice, consultați agenția sursă și un profesionist calificat.