תבנית:תרופה/אקטוס 30 מ"ג - Actos 30 mg: הבדלים בין גרסאות
מתוך ויקיתרופות
מ (החלפת טקסט – "|צורת מתן=PER OS" ב־"|צורת מתן=פומי - PER OS") |
מ (החלפת טקסט – "|סל הבריאות=כלול בסל" ב־"|סל הבריאות=כלול בסל") |
||
| שורה 13: | שורה 13: | ||
|צורת מתן=פומי - PER OS | |צורת מתן=פומי - PER OS | ||
|צורת מינון={{{צורת מינון|TABLETS}}} | |צורת מינון={{{צורת מינון|TABLETS}}} | ||
| − | |סל הבריאות= | + | |סל הבריאות=כלול בסל |
|במרשם={{{במרשם|כן}}} | |במרשם={{{במרשם|כן}}} | ||
|התוויה={{{התוויה|<div style="direction:ltr;">Pioglitazone is indicated as second or third line treatment of type 2 diabetes mellitus as described below:as monotherapy - in adult patients (particularly overweight patients) inadequately controlled by diet and exercise for whom metformin is inappropriate because of contraindications or intolerance as dual oral therapy in combination with- metformin, in adult patients (particularly overweight patients) with insufficient glycaemic control despite maximal tolerated dose of monotherapy with metformin- a sulphonylurea, only in adult patients who show intolerance to metformin or for whom metformin is contraindicated, with insufficient glycaemic control despite maximal tolerated dose of monotherapy with a sulphonylurea. as triple oral therapy in combination with - metformin and a sulphonylurea, in adult patients (particularly overweight patients) with insufficient glycaemic control despite dual oral therapy.- Pioglitazone is also indicated for combination with insulin in type 2 diabetes mellitus adult patients with insufficient glycaemic control on insulin for whom metformin is inappropriate because of contraindications or intolerance .After initiation of therapy with pioglitazone, patients should be reviewed after 3 to 6 months to assess adequacy of response to treatment (e.g. reduction in HbA1c). In patients who fail to show an adequate response, pioglitazone should be discontinued. In light of potential risks with prolonged therapy, prescribers should confirm at subsequent routine reviews that the benefit of pioglitazone is maintained .</div>}}} | |התוויה={{{התוויה|<div style="direction:ltr;">Pioglitazone is indicated as second or third line treatment of type 2 diabetes mellitus as described below:as monotherapy - in adult patients (particularly overweight patients) inadequately controlled by diet and exercise for whom metformin is inappropriate because of contraindications or intolerance as dual oral therapy in combination with- metformin, in adult patients (particularly overweight patients) with insufficient glycaemic control despite maximal tolerated dose of monotherapy with metformin- a sulphonylurea, only in adult patients who show intolerance to metformin or for whom metformin is contraindicated, with insufficient glycaemic control despite maximal tolerated dose of monotherapy with a sulphonylurea. as triple oral therapy in combination with - metformin and a sulphonylurea, in adult patients (particularly overweight patients) with insufficient glycaemic control despite dual oral therapy.- Pioglitazone is also indicated for combination with insulin in type 2 diabetes mellitus adult patients with insufficient glycaemic control on insulin for whom metformin is inappropriate because of contraindications or intolerance .After initiation of therapy with pioglitazone, patients should be reviewed after 3 to 6 months to assess adequacy of response to treatment (e.g. reduction in HbA1c). In patients who fail to show an adequate response, pioglitazone should be discontinued. In light of potential risks with prolonged therapy, prescribers should confirm at subsequent routine reviews that the benefit of pioglitazone is maintained .</div>}}} | ||
גרסה מתאריך 12:08, 6 באפריל 2021
נתוני תרופה
במרשם 
| מינונים נוספים | |
|---|---|
| קבוצה פרמקולוגית (ATC4) | |
| מרכיב פעיל (ATC5) | *Pioglitazone AS HYDROCHLORIDE 30MG A10BG03
|
| צורת מתן | פומי - PER OS |
| צורת מינון | TABLETS |
| התוויה | Pioglitazone is indicated as second or third line treatment of type 2 diabetes mellitus as described below:as monotherapy - in adult patients (particularly overweight patients) inadequately controlled by diet and exercise for whom metformin is inappropriate because of contraindications or intolerance as dual oral therapy in combination with- metformin, in adult patients (particularly overweight patients) with insufficient glycaemic control despite maximal tolerated dose of monotherapy with metformin- a sulphonylurea, only in adult patients who show intolerance to metformin or for whom metformin is contraindicated, with insufficient glycaemic control despite maximal tolerated dose of monotherapy with a sulphonylurea. as triple oral therapy in combination with - metformin and a sulphonylurea, in adult patients (particularly overweight patients) with insufficient glycaemic control despite dual oral therapy.- Pioglitazone is also indicated for combination with insulin in type 2 diabetes mellitus adult patients with insufficient glycaemic control on insulin for whom metformin is inappropriate because of contraindications or intolerance .After initiation of therapy with pioglitazone, patients should be reviewed after 3 to 6 months to assess adequacy of response to treatment (e.g. reduction in HbA1c). In patients who fail to show an adequate response, pioglitazone should be discontinued. In light of potential risks with prolonged therapy, prescribers should confirm at subsequent routine reviews that the benefit of pioglitazone is maintained .
|
| תבנית:נתוני סל/תרופה/אקטוס 30 מ"ג - Actos 30 mg | |
| התאמת מינון | Posology and method of administration |
| התוויות נגד | Contraindications |
| תופעות לוואי | Undesirable effects |
| תגובות בין תרופתיות | Interaction with other medicinal products and other forms of interaction |
| שימוש בהיריון והנקה | Pregnancy and Lactation |
| פרמקודינמיקה | Pharmacodynamic Properties |
| פרמקוקינטיקה | Pharmacokinetic Properties |
| עלון לרופא והחמרות לעלון | |
| עלון לצרכן | *עלון לצרכן |
|---|
| ערכים בוויקירפואה | ערכים קשורים בוויקירפואה |
|---|---|
| אקטוס 30 מ"ג ® במאגר משרד הבריאות |
| חיפוש מאמרים | - |
|---|---|
| מידע ברשת | - |
| שם יצרן | TAKEDA PHARMA A/S, DENMARK |
| שם בעל הרישום | ABIC MARKETING LTD, ISRAEL |
| רישיון | תאריך הגשה: 10/2012. רישיון מתאריך: 03/2018 |
| תאריך עדכון אחרון | 14/05/19 |
תמונת אריזה
דף זה נוצר על ידי בוט ומגדיר תבנית עם פרטי התרופה.
- דף התרופה: אקטוס 30 מ"ג - Actos 30 mg
- לדריסה ידנית של פרטי התרופה: ניתן לערוך את דף התרופה לעיל. לדוגמה החליפו את:
{{תרופה/אקטוס 30 מ"ג - Actos 30 mg}}
ב:
{{תרופה/אקטוס 30 מ"ג - Actos 30 mg
| שם הפרמטר=ערך חדש (דורס את הערך שהבוט הגדיר)
}}