May 5 (UPI) -- The Food and Drug Administration on Thursday said it's limiting its authorization of the single-dose Johnson & Johnson COVID-19 vaccine to adults who can't receive other versions of the shot.
The federal agency said it's restricting the vaccine because of the risk of thrombosis with thrombocytopenia syndrome, which can cause rare but potentially life-threatening blood clots and low levels of blood platelets about one to two weeks after the administration of the shot.