ברנזיס 50 מ"ג/מ"ל - Brenzys 50 mg/ml
| קבוצה פרמקולוגית (ATC4) | L04AB Tumor necrosis factor alpha (TNF-α) inhibitors | ||||||||||||||||||||||||||||||||||||||||||
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| מרכיב פעיל (ATC5) |
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| צורת מתן | תת-עורי - S.C | ||||||||||||||||||||||||||||||||||||||||||
| צורת מינון | תמיסה להזרקה, SOLUTION FOR INJECTION למניעת מינון יתר או הרעלה יש ליטול את התרופה בהתאם למינון המומלץ כפי שמופיע בעלון לצרכן | ||||||||||||||||||||||||||||||||||||||||||
| התוויה | Rheumatoid arthritisBrenzys 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. Brenzys 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. Brenzys, 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 wighing at least 62.5 Kg 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 weighing at least 62.5 Kg 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 weighing at least 62.5 Kg 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. Brenzys 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 nonsteroidal 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 weighing at least 62.5 Kg who are inadequately controlled by, or are intolerant to, other systemic therapies or phototherapies | ||||||||||||||||||||||||||||||||||||||||||
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| עלון לרופא והחמרות לעלון |
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| ערכים בוויקירפואה | ערכים קשורים בוויקירפואה |
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| ברנזיס 50 מ"ג/מ"ל במאגר משרד הבריאות |
| חיפוש מאמרים | מאמרים ב-PubMed |
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| מידע ברשת | RxList WebMD Drugs.com |
| שם יצרן | BIOGEN (DENMARK) MANUFACTURING APS, DENMARK |
| שם בעל הרישום | SAMSUNG BIOEPIS IL LTD, ISRAEL |
| רישיון | תאריך הגשה: 11/2017. רישיון מתאריך: |
