The U.S. Food and Drug Administration (FDA) holds an audio press conference after requesting a “pause” on the rollout of Johnson & Johnson COVID-19 vaccine due to cases of a rare blood clot found in 6 people as of earlier this morning.
Dr. Janet Woodcock, M.D., Acting Chairperson of the U.S. Food and Drug Administration (FDA), Dr. Peter Marks, M.D., Ph.D., Director of the FDA Center for Biologics Evaluation and Research and Dr. Anne Schuchat, M.D., Principal Deputy Director of the Centers for Disease Control and Prevention (CDC), address the decision to request a pause of rollout of the single-dose Johnson & Johnson vaccine, provide insight into why this decision was made, and field questions from the media.
This video is available on the YouTube page of the U.S. Food and Drug Administration. For more information, visit https://www.fda.gov/
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