The U.S. Food and Drug Administration is limiting the use of Johnson and Johnson’s Janssen COVID-19 vaccine as a last resort for adults who cannot accept a shot from another manufacturer.
Though the potential benefits of the vaccine outweigh the risks, the FDA said Thursday that it is restricting the use of the Janssen vaccine. It will be limited to individuals 18 and older and medically ineligible for another approved vaccine and to those who only have access to the J&J vaccine and want one, according to an FDA news release.
Researchers with the FDA and Centers for Disease Control and Prevention found that the vaccine resulted in 60 confirmed cases of thrombosis with thrombocytopenia syndrome. This leads to rare but potentially life-threatening blood clots, the FDA said, one to two weeks after receiving the shot. And with multiple vaccines available, the FDA decided to bench the J&J vaccine, only to be used when other options are unavailable.
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