Health
The use of the J & J COVID vaccine is restricted by the FDA due to the risk of blood clots.
The Food and Drug Administration has strict restrictions on who can receive J.ohnson & Johnson single dose COVID-19 vaccine On Thursday, he said the vaccine should only be given to those who cannot receive another vaccine, or especially those who request it.
After the single-dose vaccine was approved in February 2021, the FDA and the Centers for Disease Control and Prevention Shot management was temporarily suspended in April After reporting the blood clots of the few who received it.The suspension will be lifted after 11 days and the health agency will The benefits of the J & J vaccine outweighed the risks.
However, the FDA has reversed policy, determining the risk of a side effect called thrombosis with thrombocytopenia syndrome, which outweighs the benefits. situation, Also known as vaccine-induced thrombocytopenia. It is a combination of blood clots and platelets with a low platelet count. Blood clots form in abnormal places, such as veins that drain blood from the brain.
Until late 2021, the United States treated all three COVID-19 vaccines available to Americans (Pfizer, Moderna, Johnson & Johnson) as equivalent options. But in December of last year, CDC officially recommended Pfizer and Modana COVID vaccines over J & J..
Thursday’s decision goes one step further and officially limits the use of vaccines.
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Dr. Peter Markes, FDA’s head of vaccines, said authorities made decisions after reviewing data on life-threatening blood clot risks and concluded that they were limited to J & J vaccines. rice field.
“If there is an alternative that seems equally effective in preventing serious consequences from COVID-19, we would rather see people who choose it,” Marks said. This is still a better option. “
This problem occurs in the first two weeks after vaccination. “Therefore, if you were vaccinated six months ago, you can sleep soundly tonight, knowing that this is not a problem,” he added.
Of the approximately 17 million Americans who received J & J shots, federal scientists identified 60 side effects, including 9 fatal cases, as of mid-March. This corresponds to 3.23 cases of thrombosis per 1 million J & J shots. According to Marks, this problem was common in women under the age of 50, with a mortality rate of approximately once in a million shots.
Following the FDA’s decision, the J & J vaccine will issue warnings of potential “long-term, debilitating health effects” of side effects.
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A J & J spokesman said in an email statement:
Over 200 million Americans received double-dose shots of Moderna and Pfizer, compared to J & J’s 17 million.
Contributed by: Elizabeth Weise and Karen Weintraub, USA TODAY; Associated Press
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