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U.S. calls for pause to J&J COVID-19 vaccine over rare blood clots

epa09041618 A screen shows the logo for the pharmaceutical company Johnson and Johnson on the floor of the New York Stock Exchange in New York, New York, USA, 29 May 2019 (reissued 27 February 2021). The Johnson and Johnson new single shot Covid-19 vaccine has been approved for use in the US by the US Food and Drug Administration on 27 February 2021. EPA-EFE/JUSTIN LANE

U.S. federal health agencies on Tuesday recommended pausing the use of Johnson & Johnson’s COVID-19 vaccine after six recipients developed a rare disorder involving blood clots, in a fresh setback to global efforts to tackle the pandemic.

The move comes a week after European regulators said they had found a possible link between AstraZeneca’s COVID-19 vaccine and a rare blood clotting problem that had led to a small number of deaths.

Johnson & Johnson’s (J&J) single dose vaccine – most COVID-19 shots are delivered over two doses – and AstraZeneca’s low-cost vaccine are seen as vital tools in the fight against a pandemic that has claimed more than three million lives.

An advisory committee to the U.S. Centers for Disease Control and Prevention (CDC) will hold a meeting on Wednesday to review the cases linked to the J&J vaccine, and the U.S. Food and Drug Administration (FDA) will review the analysis, the agencies said in a joint statement.

All six recipients were women between the ages of 18 and 48, and the symptoms occurred six to 13 days after vaccination.

via Reuters

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