Johnson & Johnson has granted the FDA the emergency authorization of its vaccine against covid-19. Requires a sola dose | Univision Health News

The Johnson & Johnson Laboratory informs you that pidió an emergency authorization to the Pharmacovigilance and Food Administration (FDA) of the United States for the evacuation of a single dose against the coronavirus.

The petitioner said that he had been informed that the company has a vacancy rate of 72% in United States, although its results show different results in other regions. Promoting tests in the United States and other countries, the vaccine unit has a 66% efficacy to prevent moderate to severe infections and 85% against more severe syndromes.

“The presentation today of the authorization of the use of our emergency vehicle for the covid-19 of the only injection in investigation is a fundamental step in reducing the burden on people everywhere and to end the pandemic”, dijo el Dr. Paul Stoffels, Johnson & Johnson’s scientific director, is working on a communication.

The Johnson & Johnson (J&J) vacancy, for one sole injection, is one of the most hopeful. Ante el atropellado inicio de los esfuerzos de vacunación, the experts hope for a vaccine of a dose that will help increase the summiters and prevent debans from receiving doses, such as succeeding in the Pfizer and Modern vaccines that are approved by the FDA (salvo in the case of children).

The vacancy of J&J, in addition, is easier to distribute only you should be able to use refrigerators, different from Pfizer and Modern antidotes that you need to permanently store before you can manage them.

Ahora, the FDA should listen to the recommendations of a committee of Independent Experts, which will review the available dates and hold a public audience. It is hoped that the FDA will have a good view of this vacancy, but for the first time this audience of experts will be announced and, subsequently, the FDA will have to evaluate the recommendations that they have to make a decision. With the vacancies of Pfizer and Modern, the decision of the FDA will take place one day or so the committee recommends its approval of emergency use.

De manera anticipada, the governor of the stadium has bought 100 million doses of J&J and you can buy another 300 million doses if you decide.

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