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Safety of simultaneous vaccination with COVID-19 vaccines in the Vaccine Safety Datalink. | LitMetric

AI Article Synopsis

  • The study examines the safety of simultaneous vaccination (SV) with COVID-19 vaccines and other vaccines, analyzing data from the Vaccine Safety Datalink for those aged 5 and older.
  • The findings show that SV with COVID-19 vaccines was infrequent, with only about 0.7% for the first dose and 0.3% for the second dose, primarily including vaccines like influenza and HPV.
  • Overall, while most health outcomes following SV were rare and similar to those who didn't receive SV, there were some statistically significant increases in rates of specific conditions like appendicitis and Bell's palsy after certain doses.

Article Abstract

Introduction: Safety data on simultaneous vaccination (SV) with primary series monovalent COVID-19 vaccines and other vaccines are limited. We describe SV with primary series COVID-19 vaccines and assess 23 pre-specified health outcomes following SV among persons aged ≥5 years in the Vaccine Safety Datalink (VSD).

Methods: We utilized VSD's COVID-19 vaccine surveillance data from December 11, 2020-May 21, 2022. Analyses assessed frequency of SV. Rate ratios (RRs) were estimated by Poisson regression when the number of outcomes was ≥5 across both doses, comparing outcome rates between COVID-19 vaccinees receiving SV and COVID-19 vaccinees receiving no SV in the 1-21 days following COVID-19 vaccine dose 1 and 1-42 days following dose 2 by SV type received ("All SV", "Influenza SV", "Non-influenza SV").

Results: SV with COVID-19 vaccines was not common practice (dose 1: 0.7 % of 8,455,037 persons, dose 2: 0.3 % of 7,787,013 persons). The most frequent simultaneous vaccines were influenza, HPV, Tdap, and meningococcal. Outcomes following SV with COVID-19 vaccines were rare (total of 56 outcomes observed after dose 1 and dose 2). Overall rate of outcomes among COVID-19 vaccinees who received SV was not statistically significantly different than the rate among those who did not receive SV (6.5 vs. 6.8 per 10,000 persons). Statistically significant elevated RRs were observed for appendicitis (2.09; 95 % CI, 1.06-4.13) and convulsions/seizures (2.78; 95 % CI, 1.10-7.06) in the "All SV" group following dose 1, and for Bell's palsy (2.82; 95 % CI, 1.14-6.97) in the "Influenza SV" group following dose 2.

Conclusion: Combined pre-specified health outcomes observed among persons who received SV with COVID-19 vaccine were rare and not statistically significantly different compared to persons who did not receive SV with COVID-19 vaccine. Statistically significant adjusted rate ratios were observed for some individual outcomes, but the number of outcomes was small and there was no adjustment for multiple testing.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267508PMC
http://dx.doi.org/10.1016/j.vaccine.2023.06.042DOI Listing

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