Johnson & Johnson Vaccine Delay Continues by CDC Panel

by Michael London | 04/19/2021 4:08 PM
In collaboration with the FDA, the CDC continues to investigate some possible adverse effects associated with the Johnson & Johnson CO19 vaccine that have been recorded since the roll-out was suspended last week.
 
Vaccine experts took part in Wednesday’s CDC meeting in an attempt to decide whether to ban Johnson & Johnson’s Coronavirus’s one-shot vaccine or reduce their use.
According to a joint statement from the Food and Drug Administration and the Centers for Disease Control and Prevention, the women affected were between 18 and 48. Their symptoms occurred 6-13 days after the injection. According to federal officials, one resident has died, and another is in critical care in a hospital.

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