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U.S. pauses use of J&J COVID-19 vaccine over rare blood clots, rollout delayed in Europe
By Michael Erman and Manas Mishra
Reuters
(Reuters) - U.S. federal health agencies on Tuesday recommended pausing the use of Johnson & Johnson s COVID-19 vaccine for at least a few days after six women under age 50 developed rare blood clots after receiving the shot, dealing a fresh setback to efforts to tackle the pandemic.
Johnson & Johnson (J&J) said it would delay rollout of the vaccine to Europe, a week after regulators there said they were reviewing rare blood clots in four recipients of the shot in the United States.
Britain is still on track to offer a Covid-19 vaccine to all UK adults by the end of July – despite a pause in the rollout of the Janssen vaccine in Europe, officials have confirmed.
The UK has 30 million doses of the inoculation on order, but it has not yet been signed off for use by the Medicines and Healthcare products Regulatory Agency (MHRA).
The doses are expected to arrive in the second half of 2021 if approved by the regulator.
But the Department of Health and Social Care (DHSC) insisted Johnson & Johnson’s decision to delay the rollout of its vaccine in Europe would not derail the UK’s programme to offer a jab to all adults by the end of July.