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Health authorities must weigh limits for J&J vaccine due to blood clots




The Centers for Disease Control and Prevention was due to meet with advisers on Thursday to discuss possible restrictions on Johnson & Johnson’s COVID-19 vaccine due to ongoing concerns about blood clots, particularly among women.

Federal officials temporarily halted the use of the single-dose J&J vaccine in April to study six women who had experienced a blood clot after being vaccinated. The government decided that the rewards far outweighed the risks associated with the shot, and the use of the vaccine was resumed within days with a new warning label.

Although complications are still rare, around nine American women have died after experiencing blood clots associated with the vaccine, and the frequency of blood clots in people who received it has increased since April, the Washington Post reported on Wednesday.

About one woman in 1[ads1]00,000 people aged 30 to 49 had experienced blood clot problems after receiving a J&J jab, the FDA said in a fact sheet released on Tuesday.

The Vaccine Practice Advisory Committee was expected to vote to limit the use of J & J’s first and booster shots or issue a preferred recommendation for other vaccines, according to the newspaper. Any recommendation must be reviewed by the CDC, which allegedly asked state health departments to assess how dependent they were on the shot.

Health authorities must weigh limits for J&J vaccine due to blood clots
Federal officials temporarily halted the use of the single-dose J&J vaccine in April.
AP Photo / David Goldman, fil

“We are committed to understanding and communicating all known risks, including rare events [the blood clot condition], and strongly supports raising awareness of the signs and symptoms of this rare event, said Jake Sargent, a spokesman for Johnson & Johnson, reportedly.

Only about 17 million doses of J&J have been distributed in the United States, compared to about 470 million doses of Pfizer and Moderna vaccines, according to the CDC.



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