Johnson & Johnson Delays European Rollout of COVID-19 Vaccine    

Hours after U.S. federal health officials urged a pause in the use of Johnson & Johnson’s COVID-19 vaccine after it was linked to a rare but dangerous blood clot, the U.S. pharmaceutical giant announced Tuesday it was delaying rollout of the single-dose vaccine in Europe.

“We have been working closely with medical experts and health authorities, and we strongly support the open communication of this information to healthcare professionals and the public,” the company said in a written statement. The delay strikes a major blow to Europe’s already sluggish vaccination efforts, which has been plagued by logistical problems and a shortage of vaccines. The continent’s vaccination campaign has also been hindered by the troubled rollout of the vaccine developed by British-Swedish drugmaker AstraZeneca and the University of Oxford, which has also been linked to cases of rare blood clots. The U.S. Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA) said six women between 18 and 48 years of age who had received the Johnson & Johnson vaccine developed blood clotting known as cerebral venous sinus thrombosis (CVST) within six to 13 days after being inoculated. One of the women died, while another has been hospitalized in critical condition.