CDC, FDA Lift Pause On Johnson & Johnson Vaccine

The Centers for Disease Control and Prevention and Food and Drug Administration have lifted a 10-day pause on the Johnson & Johnson vaccine.

“Above all else, health and safety are at the forefront of our decisions,” CDC Director Dr. Rochelle Walensky said in a press release. “Our vaccine safety systems are working. We identified exceptionally rare events — out of millions of doses of the Janssen COVID-19 administered — and we paused to examine them more carefully. As we always do, we will continue to watch all signals closely as more Americans are vaccinated.”

Yesterday, a government advisory panel voted 10-4, with one abstaining, to recommend resuming injections of the Johnson & Johnson vaccine.

The panel members that voted against the plan to move forward said they did so because they wanted a more specific warning to women who appear to be more at risk of the blood clots.

The government agencies will now issue a fact sheet to medical providers warning them of the potential for extremely rare but serious blood clots.

There have been 15 confirmed reports of a rare condition that includes blood clots with low platelet counts following the Johnson & Johnson vaccine.




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