[:en]Johnson & Johnson’s single-shot Janssen COVID-19 vaccine will get FDA EUA[:]

[:en]Johnson & Johnson’s single-shot Janssen COVID-19 vaccine will get FDA EUA[:]


As anticipated, Johnson & Johnson has obtained an Emergency Use Authorization (EUA) from the FDA for its single-shot Janssen COVID-19 vaccine. With this authorization in place, Johnson & Johnson’s product is the third COVID-19 vaccine to be distributed in america, one that may be saved in a fridge, which reduces the logistical burden.

In contrast to the Pfizer and Moderna vaccines, Johnson & Johnson’s COVID-19 vaccine doesn’t require a second dose, serving to deal with the problem of people that fail to return for his or her second dose. Likewise, the flexibility to refrigerate the vaccines slightly than retaining them at colder temperatures will ease the burden in locations that lack the suitable chilly storage gear.

The FDA announced its latest COVID-19 vaccine authorization on Saturday, stating that it may be administered to adults ages 18 and older. The authorization was granted following a evaluate of the information supplied by Johnson & Johnson, with the FDA noting that ‘the information gives clear proof that the … vaccine could also be efficient in stopping COVID-19.’

In a press release, Performing FDA Commissioner Janet Woodcock, MD, mentioned:

The authorization of this vaccine expands the supply of vaccines, one of the best medical prevention methodology for COVID-19, to assist us within the struggle in opposition to this pandemic, which has claimed over half one million lives in america. The FDA, via our open and clear scientific evaluate course of, has now approved three COVID-19 vaccines with the urgency known as for throughout this pandemic, utilizing the company’s rigorous requirements for security, effectiveness and manufacturing high quality wanted to assist emergency use authorization.

Put merely, Johnson & Johnson’s Janssen COVID-19 vaccine teaches the recipient’s immune system to react in opposition to the SARS-CoV-2 virus, serving to to stop infections or cut back their severity. In keeping with the FDA, the single-shot vaccine was round 77-percent efficient at defending in opposition to extreme and significant COVID-19 instances beginning 14 days after the vaccination occurred. On the 28-day mark, the effectiveness jumped to 85-percent.

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