Seasonal influenza vaccine brands

AstraZeneca
  • Fluenz,[3] influenza vaccine live, intra-nasal
  • Fluenz Tetra,[4] influenza vaccine live, intra-nasal
  • FluMist',[5] influenza vaccine live, intra-nasal
  • FluMist Quadrivalent',[6] influenza vaccine live, intra-nasal

CSL Limited

CSL Limited obtain Novartis' flu vaccine unit in 2014, and transfer to CSL Subsidiary, bioCSL (Seqirus).[7] The following are list of bioCSL flu vaccine brands:[8]

  1. Afluria Quadrivalent,[1] an inactivated quadrivalent influenza vaccine (split viron). Also marketed as Afluria Quad and Afluria Tetra in various different markets.
  2. Afluria, an inactivated influenza vaccine (split viron). Also marketed as Enzira, Fluvax and Nilgrip in various different markets.
  3. Agrippal, an influenza vaccine (surface antigen inactivated). Also marketed as Begripal, Fluazur, Sandovac, Agriflu, Chiroflu in various different markets.
  4. Fluad,[1] an inactivated influenza vaccine, adjuvanted. Also marketed as Chiromas in Spain.
  5. Fluad Pediatric, a pediatric inactivated influenza vaccine, adjuvanted
  6. Fluad Quadrivalent, a quadrivalent influenza vaccine, adjuvanted
  7. Fluad Tetra, a quadrivalent influenza vaccine (surface antigen, inactivated, adjuvanted)
  8. Flucelvax Quadrivalent,[1] a quadrivalent inactivated influenza vaccine
  9. Flucelvax Tetra,[9] a quadrivalent inactivated influenza vaccine

GlaxoSmithKline

Fluarix and Flulaval are flu vaccines brand of GlaxoSmithKline.[10]

Mylan

Influvac is a subunit vaccine produced and marketed by Mylan. It contains inactivated purified surface fragments (subunits) from the three different strains of the influenza virus (A/H1N1, A/H3N2, and Influenza B virus) that are selected and distributed by the World Health Organization, on the basis of their latest recommendations. Previously, it was produced and marketed by Abbott Laboratories[11]

In February 2010, Abbott acquired the vaccines subunit from Solvay Pharmaceuticals included in its $6.2 billion purchase[12] and the subunit influenza vaccine — Influvac has been commercially available on the market since the early nineteen-eighties.[11] With the acquisition of Solvay, Abbott retained access to the Eastern European, Middle Eastern & Latin American markets. Approximately $850 million of sales revenue from vaccines was reported by Solvay Pharmaceuticals in 2009.[12]

In February 2015, Mylan Laboratories completed the deal with Abbott to purchase Abbott's generic drugs business in developed markets, which includes Influvac.[13][14]

Novartis

Optaflu is a cell culture derived influenza vaccine manufactured by Novartis. On April 27, 2007 Novartis received a positive opinion supporting European Union approval of Optaflu. It is the first influenza vaccine made in a mammalian cell line, rather than chicken eggs.[15] The plan was to manufacture the vaccine in Holly Springs, North Carolina. The United States government provided $500 million in construction costs and guaranteed vaccine purchases.[16]

Novartis' flu vaccine unit was sold to CSL Limited in 2014, and was placed under CSL subsidiary, bioCSL (Seqirus).[7] bioCSL as marketing authorization holder decided to discontinue the usage of Optaflu brand in 2017 due to commercial reasons[17]

Sanofi Pasteur

Sanofi Pasteur produces the split-virus influenza vaccines Fluzone (especially in the United States (US)[1] and Vaxigrip/VaxigripTetra (especially in Europe).[2] Sanofi also produces a recombinant influenza vaccine branded Flublok.[18]

Fluzone
A 5cc vial of Fluzone

Fluzone is a brand of influenza vaccine distributed by Sanofi Pasteur. It is a split-virus vaccine that is produced by chemical disruption of the influenza virus, making it incapable of causing influenza.

Dosage and storage

Fluzone is typically administered in a single dose by intramuscular injection;[19] an intradermal injection is also available.[20] It is presented as a 0.25 ml syringe for pediatric use, as a 0.5 ml syringe for adults and children, as a 0.5 ml vial for adults and children, and as a 5 ml vial for adults and children.[19] Fluzone must be refrigerated under temperatures from 2 to 8 °C (36 to 46 °F) and is inactivated by freezing. Fluzone was initially approved in 1980 by the FDA.[19]

Adverse effects

The following adverse effects have been reported:[19]

High-dose vaccine

A high-dose vaccine (Fluzone High-Dose) four times the strength of standard flu vaccine was approved by the FDA in 2009.[21][22][23] This vaccine is intended for people 65 and over, who typically have weakened immune response due to normal aging. The vaccine produces a greater immune response than standard vaccine. According to the CDC,[1] "a study published in the New England Journal of Medicine[24] [in August, 2014] indicated that the high-dose vaccine was 24.2% more effective in preventing flu in adults 65 years of age and older relative to a standard-dose vaccine." CDC recommends the high-dose vaccine for people 65 and over but expresses no preference between it and standard vaccine. Further studies were underway as of 2014.

Vaxigrip/VaxigripTetra

The split-virion influenza vaccines made by Sanofi Pasteur in Europe are called Vaxigrip and VaxigripTetra.[2][25] Vaxigrip provides immune responses to three influenza strains and VaxigripTetra adds another B strain. VaxigripTetra was approved in Europe in 2016 except for infants younger than three years old.[2]

Flublok

Recombinant influenza vaccines are produced using recombinant virus technology. This method does not require an egg-grown vaccine virus and does not use chicken eggs in the production process. Sanofi's recombinant influenza vaccine is called Flublok.[18]

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References
  1. "Influenza vaccines — United States, 2019–20 influenza season*". U.S. Centers for Disease Control and Prevention (CDC). 22 August 2019. Retrieved 27 January 2020.
  2. Gresset-Bourgeois V, Leventhal PS, Pepin S, Hollingsworth R, Kazek-Duret MP, De Bruijn I, Samson SI (2017-11-27). "Quadrivalent inactivated influenza vaccine (VaxigripTetra)". Expert Review of Vaccines. 17 (1): 1–11. doi:10.1080/14760584.2018.1407650. PMID 29157068.
  3. "Fluenz EPAR". European Medicines Agency (EMA). Retrieved 6 August 2020.
  4. "Fluenz Tetra EPAR". European Medicines Agency (EMA). Retrieved 6 August 2020.
  5. "FluMist". U.S. Food and Drug Administration. 9 July 2020. Retrieved 6 August 2020.
  6. "FluMist Quadrivalent". U.S. Food and Drug Administration. 9 July 2020. Retrieved 6 August 2020.
  7. "Australia's CSL buys Novartis flu vaccine unit for $275 mln". Reuters. 27 October 2014. Retrieved 27 January 2020.
  8. "CSL's product list". seqirus.com. Seqirus. Retrieved 27 January 2020.
  9. "Flucelvax Tetra EPAR". European Medicines Agency (EMA). 24 September 2018. Retrieved 31 March 2020.
  10. "GSK ships 2019-20 seasonal influenza vaccines for US market". us.gsk.com. 15 July 2019. Retrieved 27 January 2020.
  11. Giezeman KM, Nauta J, de Bruijn IA, Palache AM (April 2009). "Trivalent inactivated subunit influenza vaccine Influvac: 25-Year experience of safety and immunogenicity". Vaccine. 27 (18): 2414–7. doi:10.1016/j.vaccine.2009.02.008. PMID 19368782.
  12. "Abbott Halts Influvac Sale". Drug Discovery & Development.
  13. Pierson, Ransdell (14 July 2014). "Mylan to buy Abbott generics, cut taxes, in $5.3 billion deal". reuters. Retrieved 27 January 2020.
  14. Tascarella, Patty (27 February 2015). "Mylan inversion deal completed". Pittsburgh Business Times. Retrieved 27 January 2020.
  15. "Optaflu, the Novartis cell culture-derived influenza vaccine, receives positive opinion supporting European Union regulatory approval" (Press release). Novartis. Retrieved 2009-04-29.
  16. Pollack, Andrew (April 28, 2009). "Swine Flu Vaccine May Be Months Away, Experts Say". The New York Times. Archived from the original on 2020-01-24. Retrieved 2009-04-29. But Novartis is building a cell culture flu vaccine factory in Holly Springs, N.C., which might be ready for use in 2010 or 2011. The federal government is providing nearly $500 million in construction costs and guaranteed vaccine purchases.
  17. "Optaflu - Expiry of the marketing authorisation in the European Union" (PDF). European Medicine Agency. 22 June 2017. Retrieved 27 January 2020.
  18. "Recombinant Influenza (Flu) Vaccine". Center for Disease Control and Prevention. Retrieved 4 February 2020.
  19. "Fluzone Prescribing Information" Archived 2015-06-10 at the Wayback Machine. Sanofi Pasteur. June 2012.
  20. "Fluzone intradermal vaccine website". Sanofi Pasteur.
  21. "FDA Approves A High Dose Seasonal Influenza Vaccine Specifically Intended for People Ages 65 and Older" (Press release). U.S. Food and Drug Administration (FDA). December 23, 2009. Archived from the original on December 31, 2009.
  22. Centers for Disease Control and Prevention (CDC) (April 2010). "Licensure of a high-dose inactivated influenza vaccine for persons aged >or=65 years (Fluzone High-Dose) and guidance for use - United States, 2010" (PDF). MMWR. Morbidity and Mortality Weekly Report. 59 (16): 485–6. PMID 20431524.
  23. "Fluzone High-Dose Quadrivalent". U.S. Food and Drug Administration (FDA). November 14, 2019. Archived from the original on December 1, 2019. Retrieved November 30, 2019. This article incorporates text from this source, which is in the public domain.
  24. DiazGranados CA, Dunning AJ, Kimmel M, Kirby D, Treanor J, Collins A, Pollak R, Christoff J, Earl J, Landolfi V, Martin E, Gurunathan S, Nathan R, Greenberg DP, Tornieporth NG, Decker MD, Talbot HK (August 2014). "Efficacy of high-dose versus standard-dose influenza vaccine in older adults". N. Engl. J. Med. 371 (7): 635–45. doi:10.1056/NEJMoa1315727. PMID 25119609.
  25. Haugh M, Gresset-Bourgeois V, Macabeo B, Woods A, Samson SI (June 2017). "A trivalent, inactivated influenza vaccine (Vaxigrip): summary of almost 50 years of experience and more than 1.8 billion doses distributed in over 120 countries". Expert Rev Vaccines. 16 (6): 545–564. doi:10.1080/14760584.2017.1324302. PMID 28460594.
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