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Print this article A person receives a dose of the Johnson & Johnson coronavirus vaccine at a vaccination center in Chicago, Ill., April 6, 2021. (Carlos Barria/Reuters) The regulatory agency regularly hamstrings the development and use of essential medicines. Last week, the Food and Drug Administration reported that six women of childbearing age who received the one-dose Johnson & Johnson COVID vaccine contracted a rare form of blood clotting in the venous drainage of the brain one associated with a low platelet count. Sadly, one of the six died and another is in critical condition at the time of this writing. The FDA recommended “pausing” the use of the J&J vaccine until more information can be gathered. But even though this was less than a one-in-a-million event more than 6 million Americans have received the J&J vaccine and the risk of blood clots in women taking oral contraceptives is higher, the advisory panel established by the

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