יומירה 40 מ"ג - Humira 40 mg
מתוך ויקיתרופות
מאמרים
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התרופה נעלמה מ:מאגר התרופות של משרד הבריאות.
לא התקבלה הודעה על הפסקת שיווק התרופה ב:מערכת ההודעות על הפסקת שיווק תרופות.
תאריך עדכון אחרון לתרופה זו בויקיתרופות היה 14/05/19.
התרופה נעלמה מ:מאגר התרופות של משרד הבריאות.
לא התקבלה הודעה על הפסקת שיווק התרופה ב:מערכת ההודעות על הפסקת שיווק תרופות.
תאריך עדכון אחרון לתרופה זו בויקיתרופות היה 14/05/19.
נתוני תרופה
במרשם 
| מינונים נוספים | ||||||
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| קבוצה פרמקולוגית (ATC4) | L04AB Tumor necrosis factor alpha (TNF-α) inhibitors | |||||
| 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 arthritis:Humira in combination with methotrexate is indicated for:- The treatment of moderate to severe, active rheumatoid arthritis in adult patients when the response to disease-modifying anti-rheumatic drugs including methotrexate has been inadequate.- The treatment of severe, active and progressive rheumatoid arthritis in adults not previously treated with methotrexate.Humira can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate.Humira has been shown to reduce the rate of progression of joint damage as measured by X-ray and to improve physical function, when given in combination with methotrexate.• Polyarticular juvenile idiopathic arthritis:Humira in combination with methotrexate is indicated for the treatment of active polyarticular juvenile idiopathic arthritis, in patients from the age of 2 years who have had an inadequate response to one or more disease-modifying anti-rheumatic drugs (DMARDs). Humira can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate. Humira has not been studied in patients aged less than 2 years.• Enthesitis-related arthritis:Humira is indicated for the treatment of active enthesitis-related arthritis in patients, 6 years of age and older, who have had an inadequate response to, or who are intolerant of, conventional therapy.• Axial spondyloarthritis :Humira is indicated for the treatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy.• Axial spondyloarthritis without radiographic evidence of AS:Humira is indicated for the treatment of adults with severe axial spondyloarthritis without radiographic evidence of AS, but with objective signs of inflammation by radiological and/or laboratory tests including MRI and serum CRP levels , who have had an inadequate response to, or are intolerant to, non - steroidal anti-inflammatory drugs. • Psoriatic arthritis:Humira is indicated for the treatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying anti rheumatic drug therapy has been inadequate. Humira has been shown to reduce the rate of progression of peripheral joint damage as measured by X-ray in patients with polyarticular symmetrical subtypes of the disease and to improve physical function.• Psoriasis:Humira is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy.• Paediatric plaque psoriasis:Humira is indicated for the treatment of severe chronic plaque psoriasis in children and adolescents from 4 years of age who have had an inadequate response to or are inappropriate candidates for topical therapy and phototherapies.• Hidradenitis suppurativa (HS):Humira is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adult and adolescents from 12 years of age with an inadequate response to conventional systemic HS therapy.• Crohn’s disease:Humira is indicated for reducing signs and symptoms and inducing and maintaining clinical remission in adult patients with moderately to severely active Crohn’s disease who have had an inadequate response to conventional therapy. Humira is indicated for reducing signs and symptoms and inducing clinical remission in these patients if they have also lost response to or are intolerant to infliximab. Paediatric Crohn's disease:Humira is indicated for the treatment of moderately to severely active Crohn's disease in paediatric patients (from 6- years of age) who have had an inadequate response to conventional therapy including primary nutrition therapy and corticosteroid, and/or an immunomodulator, or who are intolerant to or have contraindications for such therapies• Ulcerative colitis:Humira is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6-mercaptopurine (6-MP) or azathioprine (AZA), or who are intolerant to or have medical contraindications for such therapies. • Uveitis:Humira is indicated for the treatment of non-infectious intermediate, posterior and panuveitis in adult patients who have had an inadequate response to corticosteroids, in patients in need of corticosteroid-sparing, or in whom corticosteroid treatment is inappropriate.• Intestinal Behcet's disease:Humira is indicated for the treatment of intestinal Behcet’s disease in patients who have had an inadequate response to conventional therapy.• Paediatric UveitisHumira is indicated for the treatment of chronic non-infectious uveitis in paediatric patients from 2 years of age who have had an inadequate response to or are intolerant to conventional therapy, or in whom conventional therapy is inappropriate.
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נתוני סל [ הצגה ]
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| עלון לרופא והחמרות לעלון |
אין עלון לרופא | |||||
| עלון לצרכן |
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| ערכים בוויקירפואה | ערכים קשורים בוויקירפואה |
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| [ יומירה 40 מ"ג] במאגר משרד הבריאות |
| חיפוש מאמרים | מאמרים ב-PubMed |
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| מידע ברשת | RxList WebMD Drugs.com |
| שם יצרן | ABBVIE LTD., UK |
| שם בעל הרישום | ABBVIE BIOPHARMACEUTICALS LTD, ISRAEL |
| רישיון | תאריך הגשה: 02/2004. רישיון מתאריך: 07/2014 |
