Quest for the right Drug
בייפורטוס BEYFORTUS (NIRSEVIMAB)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
תוך-שרירי : I.M
צורת מינון:
תמיסה להזרקה : SOLUTION FOR INJECTION
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 Sucrose L-arginine hydrochloride L-histidine hydrochloride monohydrate L-histidine Polysorbate 80 Water for injections 6.2 Incompatibilities In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products. 6.3 Shelf life The expiry date of the product is indicated on the packaging materials After removal from refrigeration, may be kept at room temperature (20°C - 25°C) when protected from light for a maximum of 8 hours. After this time, the syringe must be discarded. 6.4 Special precautions for storage Store in a refrigerator (2°C - 8°C). Do not freeze. Do not shake or expose to direct heat. Keep the pre-filled syringe in the outer carton in order to protect from light. For storage conditions of the medicinal product, see section 6.3. 6.5 Nature and contents of container Siliconised Luer lock Type I glass pre-filled syringe with a FluroTec-coated plunger stopper. Each pre-filled syringe contains 0.5 mL or 1 mL solution. Pack sizes: • 1 or 5 pre-filled syringe(s) without needles. • 1 pre-filled syringe packaged with two separate needles of different sizes. Not all pack sizes may be marketed. 6.6 Special precautions for disposal and other handling This medicinal product should be administered by a trained healthcare professional using aseptic techniques to ensure sterility. Visually inspect the medicinal product for particulate matter and discolouration prior to administration. The medicinal product is a clear to opalescent, colourless to yellow solution. Do not inject if the liquid is cloudy, discoloured, or it contains large particles or foreign particulate matter. Do not use if the pre-filled syringe has been dropped or damaged or the security seal on the carton has been broken. Instructions for administration Beyfortus is available in a 50 mg and a 100 mg pre-filled syringe. Check the labels on the carton and pre-filled syringe to make sure you have selected the correct 50 mg or 100 mg presentation as required. Beyfortus 50 mg (50 mg/0.5 mL) pre-filled Beyfortus 100 mg (100 mg/1 mL) pre-filled syringe with a purple plunger rod. syringe with a light blue plunger rod. Purple Light Blue Refer to Figure 1 for pre-filled syringe components. Figure 1: Luer lock syringe components Finger grip Rubber stopper Syringe cap Plunger rod Syringe body Luer lock Step 1: Holding the Luer lock in one hand (avoid holding the plunger rod or syringe body), unscrew the syringe cap by twisting it counter clockwise with the other hand. Step 2: Attach a Luer lock needle to the pre-filled syringe by gently twisting the needle clockwise onto the pre-filled syringe until slight resistance is felt. Step 3: Hold the syringe body with one hand and carefully pull the needle cover straight off with the other hand. Do not hold the plunger rod while removing the needle cover or the rubber stopper may move. Do not touch the needle or let it touch any surface. Do not recap the needle or detach it from the syringe. Step 4: Administer the entire contents of the pre-filled syringe as an intramuscular injection, preferably in the anterolateral aspect of the thigh. The gluteal muscle should not be used routinely as an injection site because of the risk of damage to the sciatic nerve. Step 5: Dispose of the used syringe immediately, together with the needle, in a sharps disposal container or in accordance with local requirements. If two injections are required, repeat steps 1-5 in a different injection site. Disposal Each pre-filled syringe is for single-use only. Any unused medicinal product or waste material should be disposed of in accordance with local requirements. 7. IMPORTER AND MARKETING AUTHORISATION HOLDER AND ITS ADDRESS Sanofi Israel Ltd., Greenwork Park, P.O box 47, Yakum
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