The Centers for Disease Control and Prevention (CDC) has published the updated Advisory Committee on Immunization Practices (ACIP) guidance granting preferential recommendation for specific flu vaccines in people age 65+.
BRIDGEWATER, N.J., Aug. 26, 2022 /PRNewswire/ -- The Centers for Disease Control and Prevention (CDC) has published the updated Advisory Committee on Immunization Practices (ACIP) guidance granting preferential recommendation for specific flu vaccines in people age 65+ in its Morbidity and Mortality Weekly Report (MMWR), a journal highlighting the latest in public health news and communicating recommendations derived from science-based research.5 Sanofi US‘s Fluzone® High-Dose Quadrivalent (Influenza Vaccine) and Flublok® Quadrivalent (Influenza Vaccine) were among the flu vaccines preferentially recommended by the CDC ACIP for adults 65+. The recommendation included the use of specific flu vaccines for adults 65+ including higher dose vaccines. If none of these are available at the time of administration, people in this age group should get any other age-appropriate influenza vaccine instead.6 Influenza disproportionately impacts the 65+ population, underrepresented communities, and people with co-morbidities such as diabetes, asthma, chronic obstructive pulmonary disease, and heart disease.7 Since 2010, the CDC estimates between 70% and 85% of seasonal flu-related deaths have occurred in people 65+, and between 50% and 70% of seasonal flu-related hospitalizations have occurred among people in this age group.8 The ACIP flu vaccination guidance will ensure the high-risk population of adults 65+ are immunized with the vaccine best suited for their needs. Michael Greenberg, MD, MPH About Fluzone® High-Dose Quadrivalent (Influenza Vaccine) and Flublok® Quadrivalent (Influenza Vaccine) Flublok Quadrivalent and Fluzone High-Dose Quadrivalent are indicated for immunization against disease caused by influenza A and B strains contained in the vaccine. Flublok Quadrivalent is given to people 18 years of age and older. Fluzone High-Dose Quadrivalent is given to people 65 years of age and older.1,2 With protection against four flu strains, Fluzone High-Dose is the only influenza vaccine licensed for use in adults 65 years of age and older to have demonstrated superior efficacy in a randomized controlled trial versus a standard dose influenza vaccine for the prevention of laboratory-confirmed influenza illness and the only influenza vaccine with 10 years of data demonstrating protection from flu and its related complications.2,3,a,b In a meta-analysis of 15 published reports, including approximately 34 million people, those who received Fluzone High-Dose experienced approximately an 18% reduction in cardiorespiratory hospitalizations and 28% decrease in pneumonia hospitalizations, both of which are reductions above what the standard dose vaccines provided.3 Fluzone High-Dose Quadrivalent builds on the legacy of the trivalent formulation, which was clinically proven to be 24.2% more effective at preventing flu than standard-dose Fluzone (Influenza Vaccine) in adults 65+.9 Based on data from Fluzone High-Dose (Influenza Vaccine), side effects were slightly more frequent after vaccination with Fluzone High-Dose compared to a standard-dose vaccine.10 The efficacy of trivalent formulation is relevant to Fluzone High-Dose Quadrivalent since both products are manufactured according to the same process and have overlapping compositions.2 Flublok Quadrivalent is the first and only recombinant influenza vaccine for adults 18+ proven in a clinical study to be 30% more effective than a standard dose vaccine (Fluarix Quadrivalent [Influenza Vaccine]) at preventing flu infection in over 9,000 adults 50+.1 In adults 50+, the most common side effects were tenderness, and/or pain at the injection site; headache, and tiredness.1, The effectiveness of Flublok Quadrivalent was also judged by data from general day-to-day medical practice amongst more than 12 million adults 65 years and older, vaccination with Flublok Quadrivalent was compared to standard dose vaccines: this analysis of data captured during day-to-day medical practice of Medicare fee-for-service claims collected from during the 2019-2020 influenza season. A 5-vaccine relative effectiveness analysis showed Flublok Quadrivalent had 13.3% fewer flu-related hospitalizations and emergency room visits versus an egg-based standard dose quadrivalent flu vaccine. The other influenza vaccines evaluated within the study (Fluad, Fluzone High-Dose and Flucelvax Quadrivalent), also showed fewer flu-related hospitalizations and emergency room visits (8.2%, 6.8% and 2.8%, respectively) versus an egg-based standard dose quadrivalent flu vaccine. These data are based on one of three primary analyses. Two additional primary analyses were also conducted: two vaccine analyses comparing cell-derived inactivated quadrivalent influenza vaccine with an egg-based quadrivalent inactivated influenza vaccine (IIV4) and a quadrivalent recombinant influenza vaccine (RIV4) with IIV4. Specific characteristics of 2019-2020 season, such as varied strain circulation, may have impacted results. Study limitations include lack of access to information to confirm specific viral cases may have reduced the impact of comparisons made in the study and distortion caused by unlimited variables could have affected results. In addition, the study period was cut off at the end of February 2020 to avoid potential bias from the overlap between influenza season and the escalation of the COVID-19 pandemic in the US. This study was conducted by the FDA and Centers for Medicare and Medicaid Services. aProven superiority in a clinical trial between Fluzone High-Dose (Influenza Vaccine) (trivalent formulation) and a standard-dose influenza vaccine2 Important Safety Information for Flublok® Quadrivalent (Influenza Vaccine) and Fluzone® High-Dose Quadrivalent (Influenza Vaccine) Flublok Quadrivalent and Fluzone High-Dose Quadrivalent should not be given to anyone who has had a severe allergic reaction to any component of the vaccine (including eggs or egg products for Fluzone High-Dose Quadrivalent). In addition, Fluzone High-Dose Quadrivalent should not be given to anyone who has had a severe allergic reaction after previous dose of any influenza vaccine. Tell your health care provider if you have ever had Guillain-Barré syndrome (severe muscle weakness) after a previous influenza vaccination. If Flublok Quadrivalent and Fluzone High-Dose Quadrivalent are given to people with a compromised immune system, including those receiving therapies that suppress the immune system, the immune response may be lower than expected. Vaccination with Flublok Quadrivalent and Fluzone High-Dose Quadrivalent may not protect all people who receive the vaccine. For Flublok Quadrivalent, in adults 18 through 49 years of age, the most common side effects were tenderness, and/or pain where you got the shot; headache, tiredness, muscle aches, and joint pain. In adults 50 years of age and older the most common side effects were tenderness, and/or pain where you got the shot; headache, and tiredness. For Fluzone High-Dose Quadrivalent, in adults 65 years of age and older, the most common side effects were pain, redness, and/or swelling where you got the shot; muscle aches, headache, and general discomfort. For Flublok Quadrivalent and Fluzone High-Dose Quadrivalent, other side effects may occur. Please see the Prescribing Information for Flublok Quadrivalent. Please see the Prescribing Information and Patient Information for Fluzone High-Dose Quadrivalent. About Sanofi Sanofi is listed on EURONEXT: SAN and NASDAQ: SNY Media Relations Investor Relations Sanofi Forward-Looking Statements References
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