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US health authorities allow Johnson & Johnson to restart coronavirus vaccination

US health authorities allow Johnson & Johnson to restart coronavirus vaccination AP The US authorities have now recommended that Johnson & Johnson Covid vaccinations can restart, United States health regulators said on Friday. Earlier, they had called for a pause after the shots rollout was paused due to worries over blood clotting, according to news reports. On April 14, health authorities had proposed a halt on the vaccine following instances of severe blood clots among a handful of the millions of Americans who received the vaccine. According to Bloomberg, the Advisory Committee on Immunization Practices voted 10 to 4, with one abstention, to back the vaccine, opening the way for the US Centers for Disease Control and Prevention and the Food and Drug Administration to lift a pause on the shot that was put in place after reports of rare, serious blood clots among recipients. Regulators put dosing with the vaccine on hold 10 days ago to gather more information

Virginia announces resumption of J&J vaccine following OK from CDC, FDA

© Getty Images Multiple states said they will resume administering the Johnson & Johnson COVID-19 vaccine after federal health authorities agreed on Friday that the benefits outweigh the risks. Virginia, Illinois, Massachusetts, Nevada and New York all announced that they will be immediately restarting administration of the J&J vaccine as doses sit on the shelves after the 10-day pause. The Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) said Friday that the J&J vaccine could be administered again after accepting the recommendation from a CDC panel. The agencies had put a pause on the vaccine April 13.

Johnson & Johnson jab may cause unusual blood clotting

Johnson & Johnson jab may cause unusual blood clotting According to the EU agency, over 7 million people received the product of the Johnson & Johnson pharma company BRUSSELS: The European Medicine Agency (EMA) confirmed on Tuesday that there could be a link between Johnson & Johnson vaccines and very rare cases of blood clots. “A warning about unusual blood clots with low blood platelets should be added to the product information for Covid-19 Vaccine Janssen,” the EU regulator announced in a statement following the investigation of its safety committee. But the EMA upheld its recommendation to use the jabs and confirmed that its benefits outweighed possible risks.

European regulator says Johnson & Johnson vaccine benefits outweigh risks

© Getty Images Europe s drug regulator said Tuesday that it s recommending a warning be added to the Johnson & Johnson COVID-19 vaccine about a possible link to blood clots, but noted they are very rare and the benefits still outweigh the risks. The reported combination of blood clots and low blood platelets is very rare, and the overall benefits of COVID-19 Vaccine Janssen in preventing COVID-19 outweigh the risks of side effects, the European Medicines Agency (EMA) said in a statement. The move could foreshadow what U.S. regulators will decide on Friday, when a Centers for Disease Control and Prevention (CDC) advisory committee meets again. The use of the vaccine is currently paused in the United States.

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