Reuters
Vaccine consultants in the US Food and Drug Administration voted to recommend granting an emergency use permit for the Coronavirus vaccine from Johnson & Johnson.
If the US Food and Drug Administration (FDA) acted on the recommendation, it would be the third vaccine approved for use in the United States.
It will be the first vaccine to be obtained from a single dose, and it can be stored in regular refrigerators, making it easier to distribute compared to the “Pfizer – BioNTech” and “Moderna” vaccines, which are considered more sensitive and both require two doses.
It has another advantage in the logistics field, as it can be stored in fridge temperatures, which greatly facilitates its distribution.
The Food and Drug Administration’s recommendation came at a time when confirmed cases of the emerging coronavirus in the United States increased by 0.3% compared to the same time on Thursday, to reach 28.4 million infections, according to data from Johns Hopkins University and Bloomberg News.
This increase in injuries nationwide is the same as the average daily increase recorded last week, by 0.3%.
The state of California recorded the largest number of confirmed cases, with 3.55 million injuries, an increase of 0.2% compared to yesterday, in addition to the largest number of deaths during the last twenty-four hours, with 423 deaths.
New York State witnessed a 0.6% increase in the number of injuries, bringing the total number of injuries to 1.62 million.
Source: Agencies
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