Simultaneous administration of mRNA COVID-19 bivalent booster and influenza vaccines
- PMID: 37599140
- PMCID: PMC10661699
- DOI: 10.1016/j.vaccine.2023.08.023
Simultaneous administration of mRNA COVID-19 bivalent booster and influenza vaccines
Abstract
The U.S. Food and Drug Administration authorized use of mRNA COVID-19 bivalent booster vaccines on August 31, 2022. Currently, CDC's clinical guidance states that COVID-19 and other vaccines may be administered simultaneously. At time of authorization and recommendations, limited data existed describing simultaneous administration of COVID-19 bivalent booster and other vaccines. We describe simultaneous influenza and mRNA COVID-19 bivalent booster vaccine administration between August 31-December 31, 2022, among persons aged ≥6 months in the Vaccine Safety Datalink (VSD) by COVID-19 bivalent booster vaccine type, influenza vaccine type, age group, sex, and race and ethnicity. Of 2,301,876 persons who received a COVID-19 bivalent booster vaccine, 737,992 (32.1%) received simultaneous influenza vaccine, majority were female (53.1%), aged ≥18 years (91.4%), and non-Hispanic White (55.7%). These findings can inform future VSD studies on simultaneous influenza and COVID-19 bivalent booster vaccine safety and coverage, which may have implications for immunization service delivery.
Keywords: Co-administration; Seasonal influenza vaccine; Simultaneous vaccination; mRNA covid-19 bivalent booster vaccine.
Published by Elsevier Ltd.
Conflict of interest statement
Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Kayla E. Hanson reports financial support was provided by Seqirus Srl. Nicola P. Klein reports financial support was provided by Pfizer. Nicola P. Klein reports financial support was provided by Sanofi Pasteur Inc. Nicola P. Klein reports financial support was provided by Merck & Co Inc. Nicola P. Klein reports financial support was provided by GlaxoSmithKline Inc. Allison L. Naleway reports financial support was provided by Pfizer. Allison L. Naleway reports financial support was provided by Vir Biotechnology Inc. Lisa A. Jackson reports financial support was provided by Pfizer.
Similar articles
-
The v-safe after vaccination health checker: Active vaccine safety monitoring during CDC's COVID-19 pandemic response.Vaccine. 2023 Feb 10;41(7):1310-1318. doi: 10.1016/j.vaccine.2022.12.031. Epub 2023 Jan 23. Vaccine. 2023. PMID: 36697313 Free PMC article. Review.
-
Safety of co-administration of mRNA COVID-19 and seasonal inactivated influenza vaccines in the vaccine adverse event reporting system (VAERS) during July 1, 2021-June 30, 2022.Vaccine. 2023 Mar 10;41(11):1859-1863. doi: 10.1016/j.vaccine.2022.12.069. Epub 2023 Jan 9. Vaccine. 2023. PMID: 36669964 Free PMC article. Review.
-
Safety Monitoring of Bivalent COVID-19 mRNA Vaccine Booster Doses Among Persons Aged ≥12 Years - United States, August 31-October 23, 2022.MMWR Morb Mortal Wkly Rep. 2022 Nov 4;71(44):1401-1406. doi: 10.15585/mmwr.mm7144a3. MMWR Morb Mortal Wkly Rep. 2022. PMID: 36327162 Free PMC article.
-
Reactogenicity of Simultaneous COVID-19 mRNA Booster and Influenza Vaccination in the US.JAMA Netw Open. 2022 Jul 1;5(7):e2222241. doi: 10.1001/jamanetworkopen.2022.22241. JAMA Netw Open. 2022. PMID: 35838667 Free PMC article.
-
Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices, United States, 2021-22 Influenza Season.MMWR Recomm Rep. 2021 Aug 27;70(5):1-28. doi: 10.15585/mmwr.rr7005a1. MMWR Recomm Rep. 2021. PMID: 34448800 Free PMC article.
Cited by
-
Factors associated with uptake of bivalent mRNA COVID-19 vaccines in a large US health care system.Vaccine. 2023 Nov 30;41(49):7460-7468. doi: 10.1016/j.vaccine.2023.11.012. Epub 2023 Nov 11. Vaccine. 2023. PMID: 37953096
References
-
- Food and Drug Administration. Pfizer-BioNTech COVID-19 vaccine letter of authorization (reissued). Silver Spring, MD: US Department of Health and Human Services, Food and Drug Administration; 2022. https://www.fda.gov/media/150386/download.
-
- Food and Drug Administration. Moderna COVID-19 vaccine letter of authorization (reissued). Silver Spring, MD: US Department of Health and Human Services, Food and Drug Administration; 2022. https://www.fda.gov/media/144636/download.
-
- Centers for Disease Control and Prevention. CDC Expands Updated COVID-19 Vaccines to Include Children Ages 6 Months through 5 Years [Press release]; 2022, December 9. https://www.cdc.gov/media/releases/2022/s1209-covid-vaccine.html.
-
- Centers for Disease Control and Prevention. Interim Clinical Considerations for Use of COVID-19 Vaccines Currently Approved or Authorized in the United States. US Department of Health and Human Services, CDC; 2022. Accessed February 17, 2023, from https://www.cdc.gov/vaccines/covid-19/clinical-considerations/interim-co....
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical