Quest for the right Drug
סמופליפיד 200 מ"ג/מ"ל SMOFLIPID 200 MG/ML (PURIFIED FISH OIL, REFINED OLIVE OIL, SOYA OIL, TRIGLYCERIDES, MEDIUM-CHAIN)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
תוך-ורידי : I.V
צורת מינון:
תחליב לאינפוזיה : EMULSION FOR INFUSION
עלון לרופא
מינוניםPosology התוויות
Indications תופעות לוואי
Adverse reactions התוויות נגד
Contraindications אינטראקציות
Interactions מינון יתר
Overdose הריון/הנקה
Pregnancy & Lactation אוכלוסיות מיוחדות
Special populations תכונות פרמקולוגיות
Pharmacological properties מידע רוקחי
Pharmaceutical particulars אזהרת שימוש
Special Warning עלון לרופא
Physicians Leaflet
Pharmaceutical particulars : מידע רוקחי
6. PHARMACEUTICAL PARTICULARS 6.1 List of excipients Glycerol Egg lecithin all-rac--Tocopherol Water for injections Sodium hydroxide for pH adjustment Sodium oleate 6.2 Incompatibilities This medicinal product must not be mixed with other medicinal products except those mentioned in section 6.6. 6.3 Shelf-life 2 years Shelf life after first opening the container Chemical and physical in-use stability has been demonstrated for 24 hours at 25°C. From a microbiological point of view the emulsion should be used immediately. If not used immediately, in-use storage times and conditions prior to use are the responsibility of the user and would normally not be longer than 24 hours at 2-8°C. When used in neonates and children below 2 years, the solution (in bags and administration sets) should be protected from light exposure until administration is completed (see section 4.2, 4.4 and 6.6). 6.4 Special precautions for storage Do not store above 25°C. Do not freeze. Storage after mixing If additions are made to Smoflipid, the admixtures should be used immediately from a microbiological point of view. If admixtures are not used immediately, in-use storage times and conditions prior to use are the responsibility of the user and would normally not be longer than 24 hours at 2-8°C, unless additions have taken place in controlled and validated aseptic conditions. 6.5 Nature and content of container Glass bottles (type II, colourless) with stopper of butyl-rubber: Package sizes: Glass bottle 100 ml 10x100 ml 250 ml 10x250 ml 500 ml 10x500 ml Not all pack sizes may be marketed. 6.6 Special precautions for disposal and other handling Use only if the emulsion is homogeneous. When used in neonates and children below 2 years, protect from light exposure, until administration is completed. Exposure of Smoflipid to ambient light, especially after admixture with trace elements and/ or vitamins, generates peroxides and other degradation products that can be reduced by protection from light exposure (see section 4.2, 4.4 and 6.3). Inspect the emulsion visually for phase separation prior to administration. Ensure that the final emulsion for infusion does not show any evidence of phase separation. For single use only. Any unused emulsion should be discarded. Additives Smoflipid may be aseptically admixed with amino acid, glucose, and electrolyte solutions to produce "All-In-One" Total Parenteral Nutrition (TPN) admixtures. Compatibility for different additives and the storage time of the different admixtures will be available upon request from the marketing authorisation holder. Additions should be made aseptically. Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
שימוש לפי פנקס קופ''ח כללית 1994
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תאריך הכללה מקורי בסל
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הגבלות
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מידע נוסף