Title: FDA Approves Moderna and Pfizer COVID Boosters Targeting Variants – Rollout Expected Soon
The FDA has given the green light for updated COVID-19 boosters developed by Moderna and Pfizer, providing renewed hope in the fight against the ongoing pandemic. These boosters have specifically been designed to target emerging variants, including XBB.1.5, FL.1.5.1, and EG.5, which have posed new challenges to existing vaccines.
The rollout of these updated boosters is anticipated to happen in the near future, pending approval from the CDC. The introduction of these additional doses aims to bolster protection against COVID-19 during the fall and winter season, when the virus typically experiences a resurgence.
According to FDA guidelines, individuals aged 5 and above are now eligible to receive a single dose of the updated vaccine. However, children and infants between 6 months and 4 years old may require one or two doses, depending on their vaccination history. If these young individuals have not been previously vaccinated, they have the option of receiving either three doses of Pfizer’s vaccine or two doses of Moderna’s vaccine.
Both the Moderna and Pfizer vaccines utilize mRNA technology and have demonstrated effectiveness against currently circulating variants. Upon receiving expert opinions, it is suggested that these boosters will significantly enhance protection against severe illness, hospitalization, and death caused by COVID-19.
Health officials advise individuals who have not received a booster shot since last fall and have not recently had COVID-19 to prioritize getting a booster as soon as possible. This advice holds particular importance for those who may be at a higher risk of infection or complications.
As the rollout of these updated boosters draws closer pending CDC approval, it is expected to bring a renewed sense of protection and confidence to individuals seeking to safeguard their health and well-being from the ongoing pandemic.
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