Quest for the right Drug
דקסמדטומידין קלצקס 100 מק"ג/מ"ל DEXMEDETOMIDINE KALCEKS 100 MCG/ML (DEXMEDETOMIDINE AS HYDROCHLORIDE)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
תוך-ורידי : I.V
צורת מינון:
תרכיז להכנת תמיסה לאינפוזיה : CONCENTRATE FOR SOLUTION 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 Sodium chloride Water for injections 6.2 Incompatibilities This medicinal product must not be mixed with other medicinal products except those mentioned in section 6.6. There is a potential for adsorption of dexmedetomidine to some types of natural rubber. Although dexmedetomidine is dosed to effect, it is advisable to use components with synthetic or coated natural rubber gaskets. 6.3 Shelf life The expiry date of the product is indicated on the packaging materials. After dilution Chemical and physical in-use stability of the diluted infusions has been demonstrated for 36 hours at 25°C and at refrigerated conditions (2°C – 8°C). From a microbiological point of view, the product should be used immediately. If not used immediately, in-use storage times and conditions prior to the use are the responsibility of the user and would not normally be longer than 24 hours at 2° to 8°C, unless dilution has taken place in controlled and validated aseptic conditions. 6.4 Special precautions for storage Store below 25°C. For storage conditions after dilution of the medicinal product, see section 6.3. 6.5 Nature and contents of containers Type I colourless glass ampoules of 2 ml with one point cut. Pack sizes: 5 or 25 ampoules of 2 ml Not all pack sizes may be marketed. 6.6 Special precautions for disposal and other handling Ampoules are intended for single patient use only. Preparation of solution This medicine can be diluted in glucose 50 mg/ml (5%), Ringers, Lactated Ringer, mannitol or sodium chloride 9 mg/ml (0.9%) solution for injection to achieve the required concentration of either 4 micrograms/ml or 8 micrograms/ml prior to administration. Please see below in tabulated form the volumes needed to prepare the infusion. In case the required concentration is 4 micrograms/ml: Volume of Dexmedetomidine Kalceks 100 micrograms/ml Volume of diluent Total volume of infusion concentrate for solution for infusion 2 ml 48 ml 50 ml 4 ml 96 ml 100 ml 10 ml 240 ml 250 ml 20 ml 480 ml 500 ml In case the required concentration is 8 micrograms/ml: Volume of Dexmedetomidine Kalceks 100 micrograms/ml Volume of diluent Total volume of infusion concentrate for solution for infusion 4 ml 46 ml 50 ml 8 ml 92 ml 100 ml 20 ml 230 ml 250 ml 40 ml 460 ml 500 ml The solution should be shaken gently to mix well. This medicine should be inspected visually for particulate matter and discoloration prior to administration. This medicine has been shown to be compatible when administered with the following intravenous fluids and medicinal products: Lactated Ringers, 5% glucose solution, sodium chloride 9 mg/ml (0.9%) solution for injection, mannitol 200 mg/ml (20%), thiopental sodium, etomidate, vecuronium bromide, pancuronium bromide, succinylcholine, atracurium besylate, mivacurium chloride, rocuronium bromide, glycopyrrolate bromide, phenylephrine HCl, atropine sulfate, dopamine, noradrenaline, dobutamine, midazolam, morphine sulfate, fentanyl citrate, and a plasma-substitute. 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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הגבלות
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מידע נוסף