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The US Food and Drug Administration denies any concerns related to the “Pfizer” vaccine and confirms its 95 percent effectiveness after taking the second dose and developing long-term immunity against Corona.
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A citizen receives a Pfizer / Biotech vaccine at Croydon University Hospital, South London (AFP)
The US newspaper “Politico” reported that “the US Food and Drug Administration supported in the information documents on the Corona virus, yesterday Tuesday, Pfizer’s offer for the emergency use of the Covid-19 vaccine, confirming that it did not there are security concerns. “
The journal indicated that people’s immunity begins to respond to the vaccine rapidly after the first dose, with about 88 percent effective against corona in the following weeks, according to data published by “Pfizer” and its German partner “Biotech. “. The second dose of the vaccine increases the effectiveness by more than 95% and provides immunity for a long time.
In a related context, US President Donald Trump called on the Food and Drug Administration to act quickly, and pressure mounts after the UK and other countries authorize emergency use of the vaccine to its residents.
Pfizer is reported to be the first company to make an emergency request to use a Corona virus vaccine in the United States, in people 16 years of age and older.
According to FDA data, citizens start producing antibodies within 10 days, which can help at-risk people get a certain level of protection while they wait for the second dose.
The US Food and Drug Administration released its discussion on the vaccine Tuesday ahead of the independent advisory committee meeting for the vaccine on Thursday.
The US Food and Drug Administration may allow emergency use of the vaccine at any time after the meeting, although it is not subject to the committee’s recommendations.
The Food and Drug Administration advisory committee will discuss the Corona vaccine on Thursday and hear from Pfizer executives. The committee of physicians, vaccinologists, and statisticians will also vote to recommend the use of the vaccine in emergency situations.
It is noteworthy that the data published by the Food and Drug Administration, yesterday Tuesday, evidenced the presence of serious cases of Coronavirus infection in the experimental phase, and others in the placebo stage, known as “placebo” (it is a substance that is given to the patient for the purpose of treating him, and has no real effect on treating the disease (in particular, even though the patient is psychologically deluded that this treatment he is taking carries a cure for his disease).
6 people died in the experimental phase of the vaccine, including 4 who received a placebo vaccine and two who received the “Fuego” vaccine, but “these deaths were not related to the vaccine”, as established in the documents of the Administration of US Food and Drug Administration
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