Quest for the right Drug

|
עמוד הבית / סרזיים 400 יחידות / מידע מעלון לרופא

סרזיים 400 יחידות CEREZYME 400 UNITS (IMIGLUCERASE)

תרופה במרשם תרופה בסל נרקוטיקה ציטוטוקסיקה

צורת מתן:

תוך-ורידי : I.V

צורת מינון:

אבקה להכנת תמיסה מרוכזת לעירוי : POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION

Posology : מינונים

2       DOSAGE AND ADMINISTRATION
Cerezyme® is administered by intravenous infusion over 1-2 hours. Dosage should be individualized to each patient. Initial dosages range from 2.5 U/kg of body weight 3 times a week to 60 U/kg once every 2 weeks. 60 U/kg every 2 weeks is the dosage for which the most data are available. Disease severity may dictate that treatment be initiated at a relatively high dose or relatively frequent administration. Dosage adjustments should be made on an individual basis, and may increase or decrease, based on achievement of therapeutic goals as assessed by routine comprehensive evaluations of the patient’s clinical manifestations.
Cerezyme should be stored at 2-8°C. After reconstitution, Cerezyme should be inspected visually before use. Because this is a protein solution, slight flocculation (described as thin translucent fibers) occurs occasionally after dilution. The diluted solution may be filtered through an in-line low protein-binding 0.2 μm filter during administration. Any vials exhibiting opaque particles or discoloration should not be used. DO NOT USE Cerezyme after the expiration date on the vial.
On the day of use, after the correct amount of Cerezyme to be administered to the patient has been determined, the appropriate number of vials are each reconstituted with Sterile Water for Injection, USP. The final concentrations and administration volumes are provided in the following table:

400 Unit Vial
Sterile water for reconstitution           10.2 mL
Final volume of reconstituted product      10.6 mL
Concentration after reconstitution         40 U/mL
Withdrawal volume                           10.0 mL
Units of enzyme within final volume         400 units

A nominal 10.0 mL for the 400 unit vial is withdrawn from each vial. The appropriate amount of Cerezyme for each patient is diluted with 0.9% Sodium Chloride Injection, USP, to a final volume of 100-200 mL. Cerezyme is administered by intravenous infusion over 1-2 hours.
Aseptic techniques should be used when diluting the dose. Since Cerezyme does not contain any preservative, after reconstitution, vials should be promptly diluted and not stored for subsequent use. Cerezyme, after reconstitution, has been shown to be stable for up to 12 hours when stored at room temperature (25°C) and at 2-8°C. Cerezyme, when diluted, has been shown to be stable for up to 24 hours when stored at 2-8°C.
Relatively low toxicity, combined with the extended time course of response, allows small dosage adjustments to be made occasionally to avoid discarding partially used bottles. Thus, the dosage administered in individual infusions may be slightly increased or decreased to utilize fully each vial as long as the monthly administered dosage remains substantially unaltered.


שימוש לפי פנקס קופ''ח כללית 1994 יירשם לפי אישור הועדה הבין קופתית למתן טיפול לחולים במחלת Gaucher.
תאריך הכללה מקורי בסל 01/01/1995
הגבלות תרופה מוגבלת לרישום ע'י רופא מומחה או הגבלה אחרת

בעל רישום

SANOFI ISRAEL LTD

רישום

119 65 29980 01

מחיר

0 ₪

מידע נוסף

עלון מידע לרופא

14.07.19 - עלון לרופא 11.05.23 - עלון לרופא

עלון מידע לצרכן

11.05.23 - החמרה לעלון

לתרופה במאגר משרד הבריאות

סרזיים 400 יחידות

קישורים נוספים

RxList WebMD Drugs.com