אמספאריטי - Amsparity: הבדלים בין גרסאות
(יצירת דף עם התוכן "{{תרופה |שם בעברית=אמספאריטי |שם באנגלית=Amsparity |שם ללא מינון=אמספאריטי - Amsparity |שם ללא מינון ...") |
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(5 גרסאות ביניים של משתמש אחד אינן מוצגות) | |||
שורה 1: | שורה 1: | ||
+ | {{מידע מורחב לרופאים | ||
+ | |תמונת אריזה= | ||
+ | |הנחיות קליניות= | ||
+ | |מאמרים=כן | ||
+ | |מצגת מוצר= | ||
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+ | |סרטונים= | ||
+ | |אתר התרופה= | ||
+ | |מידע נוסף= | ||
+ | |שם חברה= | ||
+ | |כתובת חברה= | ||
+ | |עיר חברה= | ||
+ | |טלפון חברה= | ||
+ | |מנהל מוצר= | ||
+ | |youtube= | ||
+ | }} | ||
+ | __ללא_תוכן_עניינים__ | ||
{{תרופה | {{תרופה | ||
|שם בעברית=אמספאריטי | |שם בעברית=אמספאריטי | ||
שורה 6: | שורה 23: | ||
|סל הבריאות=כלול בסל | |סל הבריאות=כלול בסל | ||
|קישור למאגר משרד הבריאות1= | |קישור למאגר משרד הבריאות1= | ||
− | [ אמספאריטי] במאגר משרד הבריאות | + | [https://israeldrugs.health.gov.il/#!/medDetails/167%2006%2036463%2000 אמספאריטי] במאגר משרד הבריאות |
|תמונת אריזה= | |תמונת אריזה= | ||
|מרכיב פעיל={{רווח קשיח}} | |מרכיב פעיל={{רווח קשיח}} | ||
− | |צורת מתן= | + | *[[Adalimumab]] 50 MG / 1 ML {{כ}}[[L04AB04]] |
− | |צורת מינון={{ש}}למניעת מינון יתר או הרעלה יש ליטול את התרופה בהתאם למינון המומלץ כפי שמופיע בעלון לצרכן | + | |צורת מתן=תת-עורי - S.C |
− | |מספר רישום= | + | |צורת מינון=תמיסה להזרקה, SOLUTION FOR INJECTION{{ש}}למניעת מינון יתר או הרעלה יש ליטול את התרופה בהתאם למינון המומלץ כפי שמופיע בעלון לצרכן |
− | |שם בעל הרישום=[[]] | + | |מספר רישום=167 06 36463 00 |
− | |שם יצרן=[[]] | + | |שם בעל הרישום=[[PFIZER PHARMACEUTICALS ISRAEL LTD]] |
− | |שם יצרן מקוצר=[[]] | + | |שם יצרן=[[PFIZER INC, USA]] |
− | |תאריך הגשה= | + | |שם יצרן מקוצר=[[PFIZER]] |
+ | |תאריך הגשה=5/2020 | ||
|התוויה= | |התוויה= | ||
<div style="direction:ltr;"> | <div style="direction:ltr;"> | ||
+ | Rheumatoid arthritisAmsparity 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.Amsparity can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate.Adalimumab 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.Axial SpondyloarthritisAnkylosing spondylitis (AS)Amsparity 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 ASAmsparity 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 arthritisAmsparity 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. Adalimumab 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.PsoriasisAmsparity is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy.Hidradenitis suppurativa (HS)Amsparity is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adult patients with an inadequate response to conventional systemic HS therapy.Crohn’s diseaseAmsparity 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. Amsparity 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.Ulcerative colitisAmsparity 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.UveitisAmsparity 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 diseaseAmsparity is indicated for the treatment of intestinal Behcet’s disease in patients who have had an inadequate response to conventional therapy. | ||
</div> | </div> | ||
|ללא קטגוריה= | |ללא קטגוריה= | ||
− | |במרשם=כן | + | |במרשם=כן |
− | |עלון לרופא={{ | + | |עלון לרופא=אין עלון לרופא{{ש}} |
|עלון לצרכן={{רווח קשיח}} | |עלון לצרכן={{רווח קשיח}} | ||
+ | *[https://mohpublic.z6.web.core.windows.net/IsraelDrugs/Rishum_20_456468721.pdf כרטיס מידע בטיחותי למטופלים רב שפתי 26.05.2021] | ||
|החמרות לעלון={{רווח קשיח}} | |החמרות לעלון={{רווח קשיח}} | ||
− | |קבוצה פרמקולוגית (ATC)={{ATC משרד הבריאות| | + | |קבוצה פרמקולוגית (ATC)={{ATC משרד הבריאות|L04AB|Tumor necrosis factor alpha (TNF-α) inhibitors}} |
|רישיון מתאריך= | |רישיון מתאריך= | ||
− | |שיווק הופסק= | + | |שיווק הופסק=לא |
+ | |תאריך עדכון=06/08/2021 | ||
|התאמת מינון= | |התאמת מינון= | ||
|התוויות נגד= | |התוויות נגד= | ||
שורה 36: | שורה 57: | ||
|חיפוש בוויקירפואה= | |חיפוש בוויקירפואה= | ||
}} | }} | ||
+ | {{מאמרים | ||
+ | |תוכן= | ||
+ | *[[אדלימומאב יעילה לטיפול בכיבי פיודרמה גנגרנוזום]] | ||
+ | *[[טיפול עם מעכבי JAK והסיכון לאירועי התנקבות במערכת העיכול]] | ||
+ | }} | ||
+ | |||
+ | [[קטגוריה:יצרן PFIZER]] | ||
+ | [[קטגוריה:בעל רישום PFIZER]] | ||
+ | [[קטגוריה:Antineoplastic and immunomodulating agents - L]] | ||
+ | [[קטגוריה:Immunosuppressants - L04]] | ||
+ | [[קטגוריה:Immunosuppressants - L04A]] | ||
+ | [[קטגוריה:Tumor necrosis factor alpha (TNF-α) inhibitors - L04AB]] |
גרסה אחרונה מתאריך 09:59, 18 באוגוסט 2024
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 arthritisAmsparity 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.Amsparity can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate.Adalimumab 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.Axial SpondyloarthritisAnkylosing spondylitis (AS)Amsparity 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 ASAmsparity 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 arthritisAmsparity 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. Adalimumab 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.PsoriasisAmsparity is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy.Hidradenitis suppurativa (HS)Amsparity is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adult patients with an inadequate response to conventional systemic HS therapy.Crohn’s diseaseAmsparity 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. Amsparity 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.Ulcerative colitisAmsparity 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.UveitisAmsparity 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 diseaseAmsparity is indicated for the treatment of intestinal Behcet’s disease in patients who have had an inadequate response to conventional therapy. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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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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אמספאריטי במאגר משרד הבריאות |
חיפוש מאמרים | מאמרים ב-PubMed |
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מידע ברשת | RxList WebMD Drugs.com |
שם יצרן | PFIZER INC, USA |
שם בעל הרישום | PFIZER PHARMACEUTICALS ISRAEL LTD |
רישיון | תאריך הגשה: 5/2020. רישיון מתאריך: |
תאריך עדכון אחרון | 06/08/2021 |