תבנית:תרופה/אנברל 50 מ"ג תמיסה להזרקה - Enbrel 50 mg solution for injection: הבדלים בין גרסאות
מתוך ויקיתרופות
| שורה 11: | שורה 11: | ||
|במרשם=כן | |במרשם=כן | ||
|התוויה={{{התוויה|<div style="direction:ltr;">* Rheumatoid arthritis:Enbrel 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.. Enbrel 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.Enbrel, 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.* Psoriatic arthritisTreatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying antirheumatic drug therapy has been inadequate. Enbrel 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.* Ankylosing spondylitisTreatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy. * Plaque psoriasis Treatment of adults patients (18 years or older) with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy.* Paediatric plaque psoriasis Treatment 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.* 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.* Axial spondyloarthritis* Ankylosing 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)</div>}}} | |התוויה={{{התוויה|<div style="direction:ltr;">* Rheumatoid arthritis:Enbrel 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.. Enbrel 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.Enbrel, 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.* Psoriatic arthritisTreatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying antirheumatic drug therapy has been inadequate. Enbrel 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.* Ankylosing spondylitisTreatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy. * Plaque psoriasis Treatment of adults patients (18 years or older) with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy.* Paediatric plaque psoriasis Treatment 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.* 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.* Axial spondyloarthritis* Ankylosing 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)</div>}}} | ||
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|שם יצרן=[[WYETH PHARMACEUTICALS (HAVANT), UK]] | |שם יצרן=[[WYETH PHARMACEUTICALS (HAVANT), UK]] | ||
|שם יצרן מקוצר=[[WYETH]] | |שם יצרן מקוצר=[[WYETH]] | ||
| שורה 23: | שורה 16: | ||
|רישיון מתאריך={{{רישיון מתאריך|[[רישום מתאריך::01/2015]]}}} | |רישיון מתאריך={{{רישיון מתאריך|[[רישום מתאריך::01/2015]]}}} | ||
|תאריך הגשה=12/2008 | |תאריך הגשה=12/2008 | ||
| − | |קישור למאגר משרד הבריאות1= | + | |קישור למאגר משרד הבריאות1=[ אנברל 50 מ"ג תמיסה להזרקה] במאגר משרד הבריאות |
| − | |עלון לרופא={{ | + | |עלון לרופא={{רווח קשיח}} |
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|עלון לצרכן={{רווח קשיח}} | |עלון לצרכן={{רווח קשיח}} | ||
| − | + | |החמרות לעלון={{רווח קשיח}} | |
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| − | |החמרות לעלון={{ | + | |
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|מספר רישום={{{מספר רישום|142 53 31950 00}}} | |מספר רישום={{{מספר רישום|142 53 31950 00}}} | ||
|תאריך עדכון=[[עדכון אחרון::14/05/19]] | |תאריך עדכון=[[עדכון אחרון::14/05/19]] | ||
|תמונת אריזה= | |תמונת אריזה= | ||
|שיווק הופסק={{{שיווק הופסק|לא}}} | |שיווק הופסק={{{שיווק הופסק|לא}}} | ||
| − | |שם ללא מינון= | + | |שם ללא מינון=אנברל - Enbrel |
| + | |שם ללא מינון באנגלית=Enbrel | ||
| + | |התאמת מינון= | ||
| + | |התוויות נגד= | ||
| + | |פרמקודינמיקה= | ||
| + | |פרמקוקינטיקה= | ||
| + | |שימוש בהריון והנקה= | ||
| + | |תגובות בין תרופתיות= | ||
| + | |תופעות לוואי= | ||
| + | |חיפוש בוויקירפואה= | ||
|ללא קטגוריה={{{ללא קטגוריה|<noinclude>-</noinclude>}}} | |ללא קטגוריה={{{ללא קטגוריה|<noinclude>-</noinclude>}}} | ||
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<noinclude>{{תרופה/תיעוד}}</noinclude> | <noinclude>{{תרופה/תיעוד}}</noinclude> | ||
גרסה מתאריך 14:53, 5 באוגוסט 2021
נתוני תרופה
במרשם 
| מינונים נוספים | |
|---|---|
| קבוצה פרמקולוגית (ATC4) | L04AB Tumor necrosis factor alpha (TNF-α) inhibitors |
| מרכיב פעיל (ATC5) |
|
| 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:Enbrel 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.. Enbrel 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.Enbrel, 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.* Psoriatic arthritisTreatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying antirheumatic drug therapy has been inadequate. Enbrel 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.* Ankylosing spondylitisTreatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy. * Plaque psoriasis Treatment of adults patients (18 years or older) with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy.* Paediatric plaque psoriasis Treatment 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.* 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.* Axial spondyloarthritis* Ankylosing 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)
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| תבנית:נתוני סל/תרופה/אנברל 50 מ"ג תמיסה להזרקה - Enbrel 50 mg solution for injection | |
| עלון לרופא והחמרות לעלון |
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| עלון לצרכן |
|---|
| ערכים בוויקירפואה | ערכים קשורים בוויקירפואה |
|---|---|
| [ אנברל 50 מ"ג תמיסה להזרקה] במאגר משרד הבריאות |
| חיפוש מאמרים | - |
|---|---|
| מידע ברשת | - |
| שם יצרן | WYETH PHARMACEUTICALS (HAVANT), UK |
| שם בעל הרישום | PFIZER PHARMACEUTICALS ISRAEL LTD |
| רישיון | תאריך הגשה: 12/2008. רישיון מתאריך: 01/2015 |
| תאריך עדכון אחרון | 14/05/19 |
דף זה נוצר על ידי בוט ומגדיר תבנית עם פרטי התרופה.
- דף התרופה: אנברל 50 מ"ג תמיסה להזרקה - Enbrel 50 mg solution for injection
- לדריסה ידנית של פרטי התרופה: ניתן לערוך את דף התרופה לעיל. לדוגמה החליפו את:
{{תרופה/אנברל 50 מ"ג תמיסה להזרקה - Enbrel 50 mg solution for injection}}
ב:
{{תרופה/אנברל 50 מ"ג תמיסה להזרקה - Enbrel 50 mg solution for injection
| שם הפרמטר=ערך חדש (דורס את הערך שהבוט הגדיר)
}}
