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U S pauses J&J COVID-19 vaccine over rare blood clots

U.S. federal health agencies on Tuesday recommended pausing the use of Johnson & Johnson's COVID-19 vaccine after six women under 50 given the shot developed rare blood clots, dealing a fresh setback to efforts to tackle the pandemic.

US pauses J&J COVID-19 vaccine over rare blood clots -- Health & Wellness -- Sott net

Tue, 13 Apr 2021 17:12 UTC © Unsplash / Steven Cornfield 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 50 given the shot developed rare blood clots, dealing a fresh setback to efforts to tackle the pandemic. Following the news, Johnson & Johnson (J&J) said it was delaying the 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. Janet Woodcock, acting commissioner of the U.S. Food and Drug Administration (FDA) said the agency expected the pause to be a matter of days, and it was aimed at providing information to healthcare providers so they can diagnose, treat and report such blood clots.

U S pauses use of J&J COVID-19 vaccine over rare blood clots, rollout delayed in Europe

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.

U S pauses use of J&J vaccine over rare blood clots, rollout delayed in Europe

U.S. pauses use of J&J 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 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 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. South Africa also suspended use of J&J s vaccine.

US calls for pause on J&J s Covid-19 vaccine after 6 clotting cases

Read more about US calls for pause on J&J s Covid-19 vaccine after 6 clotting cases on Business Standard. The USFDA said one person had died from the rare blood clotting condition after taking the J&J vaccine and another was in a critical condition

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