After just about 16 million cases and 298 thousand deaths, FDA announced yesterday that they will be implementing emergency usage of Pfizer's vaccine. The American government wasn't ready to embrace the vaccine previously because of the unknown side effects which now have been made apparent with the most common effect being anaphylaxis and facial muscle paralysis. But, since then, the United Kingdom has made a deal with Pfizer for millions of doses which would put Britain in the driver's lane over the U.S in terms of priority distribution. Many nations in the world are fighting for Pfizer's cure so that prompted the U.S to excuse their worries and maintain peak vaccination supply.
Although the U.S has dealt its way into 100 million doses of the vaccine, the first batch of vaccines will be delivered out to high-risk citizens such as medical care workers who have constant exposure to the virus. Residents of long-term care facilities are also prioritized because of the pattern of the elderly succumbing to the virus in higher numbers accounting for around 40% of coronavirus deaths in the U.S. In terms of the process for vaccination, one would have to be vaccinated once every two weeks for a 95% efficacy rate.
In terms of implementation, Dr. Anthony Fauci, the director of the National Institute of Allergy and Infectious Diseases, has said that the months following December all the way until estimated April will be reserved for the priority group of high exposure. After that, "I would project by the time you get to April, it will be ... 'open season,' in the sense of anyone, even the non-high priority groups could get vaccinated," Fauci said. But just because a vaccine has been deployed, doesn't mean the duty of the civilians to socially distance will be less of a burden, especially since a vaccine is deployed, we as civilians must be even more vigilant so we can expedite the date of when non-risk citizens can receive the vaccination.
Although the vaccination seems like a godsend, the FDA trial runs concluded that less than 4.6% of the participants had severe reactions. This may seem like a low percentage, but scale that into a nation's population and the number of recipients that faced adverse reactions will seem incredibly large.
I think the American government had every right to be cautious of the side effects especially since the FDA expedited the vaccine's trial, but that shouldn't stop them from being proactive in the procurement of the drug. This isn't like the 2002 Sars outbreak where transmission was low as a result of death rates being high; the coronavirus is an excellent medium that specializes in crowd control to infect the peak number of people. What are your thoughts on an expedited distribution of the vaccination? Would you be willing to dose yourself knowing the risks?






