The agencies they are investigating reports that six women experienced blood clots in conjunction with low platelet counts in the days following their Johnson & Johnson vaccine.
Johnson & Johnson has submitted a request to the United States Food and Drug Administration for emergency approval of it's novel single-shot Coronavirus vaccine.
On December 10th, the Food and Drug Administration is set to hold an advisory committee meeting to discuss Pfizer's request for emergency use authorization so that they may get the vaccine distributed sooner rather than later.