Reply letter to "safety of SARS-Cov-2 vaccines administration for adult patients with hereditary fructose intolerance"
- PMID: 34473597
- PMCID: PMC8828103
- DOI: 10.1080/21645515.2021.1959149
Reply letter to "safety of SARS-Cov-2 vaccines administration for adult patients with hereditary fructose intolerance"
Abstract
In the letter, Urro et al. performed a search on the sucrose, fructose and sorbitol content in the approved Sars-Cov-2 vaccines and they concluded that these vaccines can be safely administered in adults affected by Hereditary fructose intolerance.The Pfizer-BioNTech COVID-19 Vaccine is currently approved for use in adolescents ≥ 12 years and the Moderna COVID-19 vaccine is close to approval for use in children over 12 years of age. Furthermore, both vaccines have initiated clinical trials that will include infant as young as 6 months. Therefore, we considerate important to analyze the safely administration of this two vaccines in children with Hereditary fructose intolerance.
Keywords: SARS-Cov 2; vaccine; Hereditary fructose intolerance; children; sucrose.
Comment on
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Safety of Sars-Cov-2 vaccines administration for adult patients with hereditary fructose intolerance.Hum Vaccin Immunother. 2021 Nov 2;17(11):4112-4114. doi: 10.1080/21645515.2021.1943992. Epub 2021 Jul 1. Hum Vaccin Immunother. 2021. PMID: 34197272 Free PMC article. No abstract available.
References
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- European Medicines Agency . First COVID-19 vaccine approved for children aged 12 to 15 in EU. News May 28, 2021. https://www.ema.europa.eu/en/news/first-covid-19-vaccine-approved-childr....
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- Food and Drug Administration . Coronavirus (COVID-19) Update: FDA Authorizes Pfizer-BioNTech COVID-19 vaccine for emergency use in adolescents in another important action in fight against pandemic. May, 2021. https//www.fda.gov/news-events/press-announcements/coronavirus-covid-19-...
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- European Medicines Agency . EMA evaluating the use of COVID-19 Vaccine Moderna in young people aged 12 to 17. News, June 06, 2021. https://www.ema.europa.eu/en/news/ema-evaluating-use-covid-19-vaccine-mo...
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