and older.Multi-dose vial, 5 mL, for persons 6 months of age and > 10% for each B strain in Fluzone Quadrivalent compared with the

Children & influenza (flu).IQVIA™. Dans ce cas, il serait dangereux pour vous de recevoir une autre dose du même type de vaccin.Tous les contenus sont la propriété de MediResource Inc. 1996 – 2020.02420643     Fluzone Quadrivalent Intramuscular Suspension,Tableau des médicaments d'ordonnance contre l'eczéma,Options thérapeutiques pour la mycose de l'ongle des orteils.Comment ce médicament agit-il?

42.0% were Black, and 7.2% were of other racial groups. causal relationship to vaccine exposure. Engl J Med 1998;339:1797-802.Do not administer Fluzone Quadrivalent to anyone with a Flublok Quadrivalent, Fluzone Quadrivalent, and Fluzone High-Dose vaccines should not be given to anyone who has …

Qualitative and quantitative composition,4.2 Posology and method of administration,4.4 Special warnings and precautions for use,4.5 Interaction with other medicinal products and other forms of interaction,4.7 Effects on ability to drive and use machines,6.6 Special precautions for disposal and other handling,9. This information is intended for use by health professionals,Quadrivalent Influenza Vaccine (split virion, inactivated), suspension for injection in pre-filled syringe,Quadrivalent influenza vaccine (split virion, inactivated).Influenza virus (inactivated, split) of the following strains*:A/Guangdong-Maonan/SWL1536/2019 (H1N1)pdm09 - like strain,(A/Guangdong-Maonan/SWL1536/2019, CNIC-1909)……………………………..15 micrograms HA**,A/Hong Kong/2671/2019 (H3N2) - like strain,(A/Hong Kong/2671/2019, IVR-208)………………………………………………....15 micrograms HA**,B/Washington/02/2019 - like strain (B/Washington/02/2019, wild type…………..15 micrograms HA**,B/Phuket/3073/2013 - like strain (B/Phuket/3073/2013, wild type)……………….15 micrograms HA**,* propagated in fertilised hens' eggs from healthy chicken flocks.This vaccine complies with the WHO recommendations (Northern Hemisphere) and EU decision for the 2020/2021 season.For the full list of excipients, see Section 6.1.Quadrivalent Influenza Vaccine (split virion, inactivated) may contain traces of eggs, such as ovalbumin, and of neomycin, formaldehyde and octoxinol-9, which are used during the manufacturing process (see Section 4.3).Suspension for injection in pre-filled syringe.The vaccine, after shaking gently, is a colourless opalescent liquid.Quadrivalent Influenza Vaccine (split virion, inactivated) is indicated for the prevention of influenza disease caused by the two influenza A virus subtypes and the two influenza B virus types contained in the vaccine for:- active immunisation of adults, including pregnant women, and children from 6 months of age and older.- passive protection of infant(s) from birth to less than 6 months of age following vaccination of pregnant women (see Sections 4.4, 4.6 and 5.1).The use of Quadrivalent Influenza Vaccine (split virion, inactivated) should be based on official recommendations.Based on clinical experience with the trivalent vaccine, annual revaccination with influenza vaccine is recommended given the duration of immunity provided by the vaccine and because circulating strains of influenza virus might change from year to year.- Children from 6 months to 17 years of age: one dose of 0.5 mL.For children less than 9 years of age who have not previously been vaccinated, a second dose of 0.5 mL should be given after an interval of at least 4 weeks.- Infants less than 6 months of age: the safety and efficacy of Quadrivalent Influenza vaccine (split virion, inactivated) administration (active immunisation) have not been established.

pre-specified criteria (see Table 9 and Table 10).Non-inferiority immunogenicity criteria based on HI Swiftwater, PA: Sanofi Pasteur Inc.Fluzone Quadrivalent vaccine [Prescribing Information].

reconstitution or mixed with any other vaccine.Fluzone Quadrivalent is a suspension for injection.Fluzone Quadrivalent is supplied in 4 presentations:Single-dose, prefilled syringe (pink plunger rod), We also discuss the benefits, risks, and side effects of flu shots, and who should avoid them. Furthermore, antibodies to one antigenic variant of influenza virus might not protect against a new antigenic variant of the same type or subtype. In some human studies, antibody titers ≥1:40 have been associated with protection from influenza illness in up to 50% of participants. *Statutory timeframe for standard applications is 255 working days.An obligatory component of risk management plans is routine pharmacovigilance. à l'équipage d'un bateau).les personnes qui sont directement en contact avec de la volaille infectée par la grippe aviaire, au cours des opérations d'abattage.une allergie à l'un des ingrédients du médicament ou à l'une des traces résiduelles du médicament;une fièvre ou une affection aiguë (à l'exception de troubles légers);des courbatures ou une douleur musculaire;un endolorissement, une rougeur ou une grosseur au lieu d'injection;une sensation générale de gêne ou de malaise.une névralgie, des engourdissements ou des picotements.les symptômes d'une réaction allergique grave (par ex.

those following TIV for the B strain not contained in each respective TIV, The study was conducted over two influenza seasons (2011-2012 and 2012-2013); 53% of participants enrolled in the first year of the study were re-enrolled and re-randomized in the second year. particulate matter and/or discoloration prior to administration, whenever

Fluzone Quadrivalent vaccine.The following events have been spontaneously reported

The objective was to demonstrate immunologic non-inferiority of Fluzone High-Dose Quadrivalent to Fluzone High-Dose, as assessed by HAI geometric mean antibody titers (GMTs) at Day 28 and seroconversion rates, to strains common to formulations of both vaccines, based on pre-specified criteria.A total of 2670 adults from 65 years of age were randomized (4:1:1) to receive one dose of either Fluzone High-Dose Quadrivalent or one of two formulations of Fluzone High-Dose (one formulation contained a B strain of the Victoria lineage [TIV-HD1] while the other contained a B strain of the Yamagata lineage [TIV-HD2]).Females accounted for 58.2% of participants in the Fluzone High-Dose Quadrivalent group and 57.4% of participants in the Fluzone High-Dose group (TIV-HD1 and TIV-HD2, pooled). Ce médicament appartient au groupe de médicaments appelés.Des souches distinctes apparaissent chaque année (ce sont des versions nouvelles ou légèrement modifiées du virus). and oropharyngeal pain. The most are listed in Table 6.

months of age and older.The dose and schedule for Fluzone Quadrivalent are

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