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johnson & johnson


Federal health agencies say they are ending their recommended pause on use of Johnson & Johnson’s Janssen vaccine, following the vote of a panel of advisers to the Centers for Disease Control and Prevention on resuming the single-shot vaccine. The Food and Drug Administration says they have revised their emergency use authorization for the vaccine …

The Food and Drug Administration on Saturday authorized Johnson & Johnson’s COVID-19 vaccine for emergency use. The vaccine is the third to be approved for use in the United States, and the first that requires only one shot.   The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted unanimously to recommend authorizing the …