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Use of J&J COVID-19 Vaccine Is Put on Hold Due to Rare Risk of Blood Clotting

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The United States Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) have paused the federal use of the Johnson and Johnson (J&J) COVID-19 vaccine due to the rare but serious risk of blood clots among those who have received the immunization. They have advised state vaccination programs to follow suit. While almost 7 million Americans have received the one-dose COVID-19 vaccine from the American pharmaceutical giant, six women between the ages of 18 and 48 developed serious blood clots within 1 week to 3 weeks of receiving the vaccination. One woman has died and one remains hospitalized. Scientists at the FDA and CDC are currently reviewing J&J’s data to discuss whether the COVID-19 vaccine should continue being administered. The AstraZeneca-Oxford University COVID-19 vaccine, which is not authorized for use in the US but is used in Europe, has caused similar side effects. Click here to read more.

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