Johnson & Johnson’s Covid-19 vaccine emergency use authorization revoked by FDA
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The following information is from the FDA re: its decision to limit use of J&J Covid-19 vaccine due to blood clot risk. Today, the U.S. Food and Drug Administration has limited the authorized use of the Janssen COVID-19 Vaccine to
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AstraZeneca Covid-19 is not approved in the U.S. A new study in Europe shows a concerning incidence of a serious brain blood clots, CVST, following AstraZeneca’s shot. Initially, the blood clots were thought to occur about 3 or 4 in
An editorial recently published in the Journal of the American Medical Association recommends women under age 50 avoid the Covid-19 vaccine made by Johnson and Johnson due to concerns about blood clots. The recommendation is accompanied by a description of
New blood disorder warnings appear on the Johnson and Johnson (Janssen) Covid-19 vaccine label, now that the federal “pause” on administering the vaccine has ended. The warnings flag an increased risk of thrombosis, clotting of the blood in the circulatory
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