TUESDAY, Dec. 8, 2020 (HealthDay Information) — New knowledge launched Tuesday by the U.S. Meals and Drug Administration Vaccines and Associated Organic Merchandise Advisory Committee recommend that Pfizer’s two-dose COVID-19 vaccine works nicely defending recipients towards COVID-19.

The committee is scheduled to satisfy on Thursday to contemplate the Pfizer/BioNTech COVID-19 vaccine for emergency use authorization, CNBC reported.

In response to the FDA, the info from Pfizer’s COVID-19 vaccine trials had been “constant” with the company’s suggestions for an emergency use authorization. The information present that the vaccine supplies safety after the primary dose and that two doses are “extremely efficient” in stopping COVID-19.

“As such, FDA has decided that the Sponsor has offered enough data to make sure the vaccine’s high quality and consistency for authorization of the product below an EUA,” the company mentioned.

Right this moment, the UK started inoculating its residents with the Pfizer/BioNTech vaccine. The US is anticipated to resolve on the emergency approval of the vaccine earlier than the top of the week, CNBC reported.



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