WASHINGTON (KFOR) – As hundreds of thousands of People proceed to be vaccinated towards COVID-19 every week, officers with the Meals and Drug Administration say they’re involved about one of many broadly used vaccines.
On Tuesday, the FDA and the Facilities for Illness Management and Prevention issued an announcement, calling for a pause in the usage of the Johnson & Johnson single shot COVID-19 vaccine out of an abundance of warning.
Thus far, officers say greater than 6.8 million doses of the Johnson & Johnson COVID-19 vaccine have been administered in america.
Well being leaders say they’re investigating after six individuals developed a uncommon and extreme kind of blood clot after receiving the Johnson & Johnson vaccine.
Officers say the CDC will maintain a meting of the Advisory Committee on Immunization Practices on Wednesday to additional assessment the instances. The FDA will then assessment that evaluation.
“Till that course of is full, we’re recommending this pause. That is vital to make sure that the well being care supplier group is conscious of the potential for these antagonistic occasions and might plan as a result of distinctive remedy required with this kind of blood clot,” the FDA posted on Twitter.
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