FDA asks states to temporarily halt use of Johnson & Johnson COVID-19 vaccine

The Food and Drug Administration is asking states to stop using the Johnson & Johnson COVID-19 vaccine temporarily. 

This measure comes after six people in the United States developed a rare blood clotting disorder. 

RELATED: Johnson & Johnson dumps 15M vaccine doeses, citing quality control issue

The FDA said the cases of the disorder are rare, but the pause is “out of an abundance of caution.” 

The Centers for Disease Control and Prevention will hold a meeting on Wednesday to further review the situation. 

People who have received the Johnson & Johnson vaccine who develop severe headaches, abdominal pain, leg pain or shortness of breath within three weeks after receiving the dose should contact their doctor. 

The organization says the safety of COVID-19 vaccines is its top priority. 

COVID19 vaccine safety is a top priority for the federal government, and we take all reports of health problems following COVID-19 vaccination very seriously.”

Jeff Zients, the White House COVID-19 Response Coordinator, said the temporary pause on Johnson & Johnson COVID-19 vaccines will not significantly impact the Biden Administration’s vaccination plans.

“This announcement will not have a significant impact on our vaccination plan: Johnson & Johnson vaccine makes up less than 5 percent of the recorded shots in arms in the United States to date. Based on actions taken by the President earlier this year, the United States has secured enough Pfizer and Moderna doses for 300 million Americans.” – Jeff Zients

The Biden Administration is now working with state and federal partners to get Pfizer or Moderna vaccines for those scheduled to get the single dose of the Johnson & Johnson vaccine.

This is a developing story that will be updated. 

 

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