Health care providers are required to report any adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine, and adverse events listed in the table at, For information on how to report to VAERS, go the VAERS website at. Your account has been activated successfully, but we still need to validate you as a healthcare professional. Persons aged ≥9 years need only one dose for 2020-21. Multidose vials may have a labeled Beyond Use Date (BUD) in addition to the expiration date.

LAIV4 may be administered simultaneously with other inactivated or live vaccines.
In children 3 through 17 years of age, the most common solicited local adverse reaction was pain. We’ll send you an email with the result of the validation process in the next [five] days.

A quadrivalent influenza (flu) vaccine is … Event Account activated - pending validation. For children needing two doses, the second dose is recommended even if the child turns age 9 years between dose 1 and dose 2. (See Adverse Reactions section of the Prescribing Information for FLUARIX QUADRIVALENT for other potential adverse reactions and events), Vaccination with FLUARIX QUADRIVALENT may not result in protection in all vaccine recipients. Injectable vaccines given simultaneously should be administered at separate anatomic sites. Additional information may also be found in the. NAWCNT200004 August 2020. Data comparing benefits of the newer HD-IIV4 or aIIV4 to standard-dose unadjuvanted IIVs are limited. There are data supporting greater benefit of HD-IIV3, RIV4, or aIIV3 relative to standard-dose unadjuvanted IIVs in this age group, but comparisons of these three vaccines with one another are limited. Vaccine should be administered by the end of October, but vaccination should continue to be offered as long as influenza viruses are circulating locally and unexpired vaccine is available.
In children 3 through 5 years of age, the most common systemic adverse reactions were drowsiness, irritability, and loss of appetite. Trademarks are owned by or licensed to the GSK group of companies. Package information may also specify a maximum number of doses contained in multidose vials (regardless of remaining volume).

Routine annual influenza vaccination is recommended for all persons aged ≥6 months who do not have contraindications. Vaccination too early in the season (e.g., July or August) may lead to suboptimal immunity later in the season, particularly among older adults. This site requires JavaScript to be enabled to work properly.

In case you would like to receive SMS-reminders for the event you have registered, please scroll down to provide your mobile number. In the meantime, you can enjoy the public content on our website. FLUARIX QUADRIVALENT is approved for use in persons aged 6 months and older. ©2020 GSK or licensor. Health care personnel or hospital visitors who receive LAIV4 should avoid providing care for severely immunosuppressed persons requiring a protected environment for 7 days after vaccination. • Fluarix 0.5 mL FluLaval 0.5 mL • Fluzone 0.25 mL or 0.5 mL 4. FLULAVAL QUADRIVALENT is approved for use in persons aged 6 months and older. Persons who have experienced only hives after exposure to egg may receive any licensed, recommended, age-appropriate influenza vaccine (i.e., IIV, RIV4, or LAIV4). FLULAVAL TETRA is not effective against all possible strains of influenza virus. Persons who receive influenza antivirals during these periods should be revaccinated with an age-appropriate IIV or RIV4 (intervals may be longer in conditions where medication clearance is delayed, such as renal insufficiency): Oseltamivir or zanamivir: 48 hours before to 2 weeks after LAIV4, Peramivir: 5 days before to 2 weeks after LAIV4, Baloxavir: 17 days before to 2 weeks after LAIV4.

Half of the total sprayer contents is sprayed into the first nostril while the recipient is in the upright position. In children 5 through 17 years of age, the most common solicited systemic adverse reactions were muscle aches, fatigue, headache, arthralgia, and gastrointestinal symptoms. Immunogenicity and safety of simultaneous or sequential administration of two vaccines containing non-aluminum adjuvants has not yet been evaluated. Moderate or severe acute illness with or without fever; Guillain–Barré syndrome within 6 weeks following a previous dose of influenza vaccine; Other underlying medical conditions that might predispose to complications attributable to severe influenza; e.g., chronic pulmonary, cardiovascular (excluding isolated hypertension), renal, hepatic, neurologic, hematologic, or metabolic disorders (including diabetes mellitus). For more information, call CDC at (800) 232-4636. Caregivers and contacts of those at risk: Health care personnel, including all paid and unpaid persons working in health-care settings who have potential for exposure to patients and/or to infectious materials, whether or not directly involved in patient care; Household contacts and caregivers of children aged ≤59 months (i.e., <5 years), particularly contacts of children aged <6 months, and adults aged ≥50 years; Household contacts and caregivers of persons with medical conditions associated with increased risk of severe complications from influenza. We'll send you and email with the result of the validation process in the next [five] days.

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