תבנית:תרופה/תוריד 40 - Torid 40: הבדלים בין גרסאות
מתוך ויקיתרופות
מ (החלפת טקסט – "|קבוצה פרמקולוגית (ATC)= {{ATC משרד הבריאות|C10" ב־"|קבוצה פרמקולוגית (ATC)={{ATC משרד הבריאות|C10") |
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שורה 3: | שורה 3: | ||
|שם באנגלית={{{שם באנגלית|Torid 40}}} | |שם באנגלית={{{שם באנגלית|Torid 40}}} | ||
|מרכיב פעיל={{רווח קשיח}} | |מרכיב פעיל={{רווח קשיח}} | ||
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*[[Atorvastatin]] AS MAGNESIUM 40MG {{כ}}[[C10AA05]] | *[[Atorvastatin]] AS MAGNESIUM 40MG {{כ}}[[C10AA05]] | ||
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|קבוצה פרמקולוגית (ATC)={{ATC משרד הבריאות|C10AA|HMG CoA reductase inhibitors}} | |קבוצה פרמקולוגית (ATC)={{ATC משרד הבריאות|C10AA|HMG CoA reductase inhibitors}} | ||
|צורת מתן=פומי - PER OS | |צורת מתן=פומי - PER OS | ||
שורה 15: | שורה 11: | ||
|התוויה={{{התוויה|<div style="direction:ltr;">Atorvastatin is indicated as an adjunct to diet for reduction of elevated total cholesterol LDL- cholesterol apolipoprotein B and triglycerides and to increase HDL Cholesterol in patients with primary hypercholesterolaemia including familial hypercholesterolaemia (heterozygous variant) or combined (mixed) hyperlipidaemia (corresponding to types IIa and IIb of the fredrickson classification) when response to diet and other nonpharmacological measures is inadequate. Atorvastatin is also indicated to reduce total-C and LDL -C in patients with homozygous familial hypercholesterolemia as an adjunct to other lipid-lowering treatment (e.g. LDL apheresis) or if such treatments are unavailable. Pediatric patients (10-17 years of age) : Atorvastatin is indicated as an adjunct to diet to reduce total -C LDL-C and apo B levels in boys and postmenarchal girls 10 to 17 years of age with heterozygous familial hypercholesterolemia if after an adequate trial of diet therapy the following findings are present: | |התוויה={{{התוויה|<div style="direction:ltr;">Atorvastatin is indicated as an adjunct to diet for reduction of elevated total cholesterol LDL- cholesterol apolipoprotein B and triglycerides and to increase HDL Cholesterol in patients with primary hypercholesterolaemia including familial hypercholesterolaemia (heterozygous variant) or combined (mixed) hyperlipidaemia (corresponding to types IIa and IIb of the fredrickson classification) when response to diet and other nonpharmacological measures is inadequate. Atorvastatin is also indicated to reduce total-C and LDL -C in patients with homozygous familial hypercholesterolemia as an adjunct to other lipid-lowering treatment (e.g. LDL apheresis) or if such treatments are unavailable. Pediatric patients (10-17 years of age) : Atorvastatin is indicated as an adjunct to diet to reduce total -C LDL-C and apo B levels in boys and postmenarchal girls 10 to 17 years of age with heterozygous familial hypercholesterolemia if after an adequate trial of diet therapy the following findings are present: | ||
# LDL-C remains >or = 190 mg/dl or 2. LDL-C remains > or = 160 mg/dl and: there is a positive family history of premature cardiovascular disease or two or more other CVD risk factors are present in the pediatric patient. Prevention of cardiovascular and/or cerebrovascular event sush as MI or stroke as an adjunct to correction of other risk factors such as hypertension in patients with three or more additional risk factors or diabetes with one additional risk factor. In patients with clinically evident coronary heart disease Atorvastatin is indicated to : Reduce the risk of non-fatal myocardial infarction. Reduce the risk of fatal and non fatal stroke. Reduce the risk for revascularization procedures. Reduce the risk of hospitalization for CHF. Reduce the risk of angina.</div>}}} | # LDL-C remains >or = 190 mg/dl or 2. LDL-C remains > or = 160 mg/dl and: there is a positive family history of premature cardiovascular disease or two or more other CVD risk factors are present in the pediatric patient. Prevention of cardiovascular and/or cerebrovascular event sush as MI or stroke as an adjunct to correction of other risk factors such as hypertension in patients with three or more additional risk factors or diabetes with one additional risk factor. In patients with clinically evident coronary heart disease Atorvastatin is indicated to : Reduce the risk of non-fatal myocardial infarction. Reduce the risk of fatal and non fatal stroke. Reduce the risk for revascularization procedures. Reduce the risk of hospitalization for CHF. Reduce the risk of angina.</div>}}} | ||
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|שם יצרן=[[TRIMA ISRAEL PHARMACEUTICAL PRODUCTS MAABAROT LTD, ISRAEL]] | |שם יצרן=[[TRIMA ISRAEL PHARMACEUTICAL PRODUCTS MAABAROT LTD, ISRAEL]] | ||
|שם יצרן מקוצר=[[TRIMA]] | |שם יצרן מקוצר=[[TRIMA]] |
גרסה מתאריך 12:26, 31 ביולי 2022
נתוני תרופה
במרשם
מינונים נוספים | |
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קבוצה פרמקולוגית (ATC4) | C10AA HMG CoA reductase inhibitors |
מרכיב פעיל (ATC5) |
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צורת מתן | פומי - PER OS |
צורת מינון | טבליה, TABLETS למניעת מינון יתר או הרעלה יש ליטול את התרופה בהתאם למינון המומלץ כפי שמופיע בעלון לצרכן |
התוויה | Atorvastatin is indicated as an adjunct to diet for reduction of elevated total cholesterol LDL- cholesterol apolipoprotein B and triglycerides and to increase HDL Cholesterol in patients with primary hypercholesterolaemia including familial hypercholesterolaemia (heterozygous variant) or combined (mixed) hyperlipidaemia (corresponding to types IIa and IIb of the fredrickson classification) when response to diet and other nonpharmacological measures is inadequate. Atorvastatin is also indicated to reduce total-C and LDL -C in patients with homozygous familial hypercholesterolemia as an adjunct to other lipid-lowering treatment (e.g. LDL apheresis) or if such treatments are unavailable. Pediatric patients (10-17 years of age) : Atorvastatin is indicated as an adjunct to diet to reduce total -C LDL-C and apo B levels in boys and postmenarchal girls 10 to 17 years of age with heterozygous familial hypercholesterolemia if after an adequate trial of diet therapy the following findings are present:
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תבנית:נתוני סל/תרופה/תוריד 40 - Torid 40 | |
עלון לרופא והחמרות לעלון |
עלון לצרכן |
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ערכים בוויקירפואה | ערכים קשורים בוויקירפואה |
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תוריד 40 ® במאגר משרד הבריאות |
חיפוש מאמרים | - |
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מידע ברשת | - |
שם יצרן | TRIMA ISRAEL PHARMACEUTICAL PRODUCTS MAABAROT LTD, ISRAEL |
שם בעל הרישום | UNIPHARM LTD, ISRAEL |
רישיון | תאריך הגשה: 06/2009. רישיון מתאריך: 12/2016 |
תאריך עדכון אחרון | 15/05/19 |
דף זה נוצר על ידי בוט ומגדיר תבנית עם פרטי התרופה.
- דף התרופה: תוריד 40 - Torid 40
- לדריסה ידנית של פרטי התרופה: ניתן לערוך את דף התרופה לעיל. לדוגמה החליפו את:
{{תרופה/תוריד 40 - Torid 40}}
ב:
{{תרופה/תוריד 40 - Torid 40 | שם הפרמטר=ערך חדש (דורס את הערך שהבוט הגדיר) }}