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FDA Restricts J&J’s COVID-19 Vaccine Over Risk Of Blood Clots

fda-restricts-j&j's-covid-19-vaccine-over-risk-of-blood-clots

The Food and Drug Administration (FDA) announced on May 5 that it will restrict the use of the Johnson & Johnson COVID-19 vaccine to adults who can’t receive mRNA vaccines, because of the risk of potentially life-threatening side effects with the J&J shot.
The agency said the COVID-19 vaccine can now only be administered to people aged 18 years of age and older who can’t receive either the Moderna or Pfizer vaccines, both of which are two-dose vaccines and use mRNA technology. J&J’s single-shot vaccine uses adenovirus technology.
People 18 and older who want to receive the J&J vaccine “because they would otherwise not receive a COVID-19 vaccine” can also get it, according to the FDA’s statement. The agency didn’t elaborate.
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