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Pfizer aprub, Sinovac nakabitin sa FDA

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Inaprobahan na ng Food and Drug Administration(FDA) ang Emergency Use Authorization(EUA) bilang COVID-19 vaccine ng Pfizer.

“After a thorough review of currently available data by medical and regulatory experts, the FDA today is granting emergency use authorization to Pfizer BioNTech COVID-19 vaccine,” ayonn kay FDA Director General Eric Domingo sa virtual briefing.

Kaugnay nito ay kinumpirma ng FDA na nag- apply na rin ang Sinovac ng EUA pero hindi umano kumpleto ang dokumento.

Ang Pfizer ang tanging vaccine na kasama sa World Health Organization’s emergency list.

Ayon kay Domingo,base sa interim data ng Phase III trials, ang Pfizer ay may 95%has efficacy rate . “The adverse events were transient and mostly mild to moderate, similar to common vaccine reactions among other vaccines that are in use now,” ayon kay Domingo.(Juliet de Loza-Cudia)

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