פרטים כלליים
שם
Name
ארלזי 50
ERELZI 50
יצרן
SANDOZ GMBH, AUSTRIA
בעל רישום
SANDOZ PHARMACEUTICALS ISRAEL LTD
שימוש
צורת מינון
Dosage Form
תמיסה להזרקה
SOLUTION FOR INJECTION
דרך מתן
Usage Form
תת-עורי
S.C
תמונה חסרה
מחירים לצרכן
לא נמצא מידע
חומר פעיל
חומר פעיל
כמות
50 MG / 1 ML
תרופות אחרות בעלות אותם מרכיבים
ATC
עדכון רישום
סוג עדכון
תאריך עדכון
29.02.2024
29.02.2024
23.11.2022
23.11.2022
01.08.2022
01.08.2022
31.08.2021
31.08.2021
25.01.2021
25.01.2021
12.01.2021
12.01.2021
06.08.2020
06.08.2020
התוויה מאושרת
Rheumatoid arthritisErelzi is indicated for the treatment of active rhematoid arthritis in adults when the response to disease-modifying antirheumatic drugs (DMARDs) including methotrexate (unless contraindicated) has been inadequate. Erelzi can be used in combination with methotrexate in patients who do not respond adequately to methotrexate alone. Reducing signs and symptoms and inhibiting the progression of structural damage in patients with moderately to severely active rheumatoid arthritis .Etanercept, alone or in combination with methotrexate, has been shown to reduce the rate of progression of joint damage as measured by X-ray and to improve physical function.Juvenile idiopathic arthritisTreatment of polyarthritis (rheumatoid factor positive or negative) and extended oligoarthritis in children and adolescents from the age of 2 years who have had an inadequate response to, or who have proved intolerant of, methotrexate. Treatment of psoriatic arthritis in adolescents from the age of 12 years who have had an inadequate response to, or who have proved intolerant of, methotrexate. Treatment of enthesitis-related arthritis in adolescents from the age of 12 years who have had an inadequate response to, or who have proved intolerant of, conventional therapy. Psoriatic arthritisTreatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying antirheumatic drug therapy has been inadequate. Etanercept has been shown to improve physical function in patients with psoriatic arthritis, and to reduce the rate of progression of peripheral joint damage as measured by X-ray in patients with polyarticular symmetrical subtypes of the disease.Axial spondyloarthritisAnkylosing spondylitis (AS)Treatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy.Non-radiographic axial spondyloarthritisTreatment of adults with severe non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated C-reactive protein (CRP) and/or magnetic resonance imaging (MRI) evidence, who have had an inadequate response to non-steroidal anti-inflammatory drugs (NSAIDs).Plaque psoriasisTreatment of adults patients (18 years or older) with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy. Paediatric plaque psoriasisTreatment of chronic severe plaque psoriasis in children and adolescents from the age of 6 years who are inadequately controlled by, or are intolerant to, other systemic therapies or phototherapies.
בסל הבריאות
כן
מספר רישום
163-21-36037-00
תנאי ניפוק
תרופה במרשם
מגבלות
תרופה מוגבלת לרישום ע'י רופא מומחה או הגבלה אחרת