Home Biden Administration CDC & FDA Advice Pause On Johnson & Johnson Vaccine After Blood Clotting

CDC & FDA Advice Pause On Johnson & Johnson Vaccine After Blood Clotting

by Graham Allen Team

GOVERNMENT AGENCIES PAUSE VACCINE AFTER RARE SIDE EFFECTS MAY EMERGE…

The FDA and the CDC are now recommending a PAUSE on the Johnson and Johnson vaccine, here’s why.

“We are recommending a pause in the use of this vaccine out of an abundance of caution,” the FDA stated on Twitter.

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This could cause a MAJOR issue with President Joe Biden’s plan to roll out 200 million vaccines in such a short time.

The reason behind the pause was that some participants in the vaccine had experienced “rare to severe” blood clotting after taking the vaccine.

Here’s what Fox News reports:

According to the FDA, there have been six reported cases of the rare and severe type of blood clot in over 6.8 million Johnson & Johnson COVID-19 vaccine recipients.

 

In Georgia, eight people experienced lightheadedness, but officials could not rule out whether heat was a factor. In North Carolina, four people were taken to the hospital for reactions “consistent with known common side effects.” In Iowa, three people experienced extreme lightheadedness, and in Colorado 11 people experienced dizziness and nausea.

While the numbers are still small of bad side effects this could be an issue for the vaccine in the future. Read EVERYTHING the CDC has said so far in the Tweet below:



Have you gotten the vaccine?

Let us know why or why not in the comment section below!

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