Sanofi-Aventis (Suisse) SA - Efluelda 0.7 ml, suspension injectable en seringue préremplie | | 67704 | | 04 | | Efluelda 0.7 ml | | suspension injectable en seringue préremplie | | J07BB02 | | Influenza, Inactivated, Split Virus Or Surface Antigen | | 16.08.2024 | | |
| Composition | haemagglutininum influenzae A (H1N1) (Virus souche A/Victoria/4897/2022 (H1N1)-like: reassortant virus IVR-238 derived from A/Victoria/4897/2022) 60 µg, haemagglutininum influenzae A (H3N2) (Virus souche A/Thailand/8/2022 (H3N2)-like: reassortant virus SAN-022 derived from A/California/122/2022) 60 µg, haemagglutininum influenzae B (Virus souche B/Austria/1359417/2021-like: derived from B/Michigan/01/2021 (Victoria lineage)(wild type)) 60 µg, haemagglutininum influenzae B (Virus souche B/Phuket/3073/2013 (Yamagata lineage) (wild type)) 60 µg, natrii chloridum, dinatrii phosphas, natrii dihydrogenophosphas anhydricus, octoxinolum-9, aqua ad iniectabile q.s. ad suspensionem pro 0.7 ml corresp. natrium 2.72 mg. | Packungsbestandteile | | | | | | | | Active Agent | Dose |
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| 60µg / 0.7ml | | 60µg / 0.7ml | | 60µg / 0.7ml |
| BAG: Active Agent | Dose |
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Influenza-haemagglutinin | 240 mcg |
| | Inactive agents | Dose |
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Disodium Phosphate | | | 60µg / 0.7ml | Sodium Chloride | | Sodium Dihydrogenophosphate Anhydrate | | | |
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