According to a study, a third vaccination should significantly increase protection against corona.
(Foto: Marina Zlochin – stock.adobe)

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EMA checks data

Biontech / Pfizer submitted the application for approval for the booster vaccination to the European Medicines Agency (EMA) about a week ago. In doing so, they are aiming to update the conditional marketing authorization for their mRNA vaccine Comirnaty. Accordingly, data were submitted to document the benefits of a booster dose (third dose) for people aged 16 and over. The American drug agency FDA is currently examining this data.

It is based on a clinical phase 3 study with 306 participants aged 18 to 55 years who received a booster dose between 4.8 and 8 months after the second vaccination.

The side effects that occurred within seven days of the third vaccination were “usually mild to moderate,” according to Biontech. The most common events included injection site pain, fatigue, headache, muscle and joint pain, and chills. When compared with the frequency of severe systemic side effects after the first two vaccinations, Biontech rates the occurrence of such cases after the third vaccination as “low”.

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