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Today: The FDA is adding a warning to Johnson & Johnson s COVID-19 vaccine, the WHO is pushing back on Pfizer s calls for a booster dose, and a House panel wants information from Biogen about its controversial Alzheimer s drug.
We’ll start with J&J:
FDA adds new warning to J&J COVID-19 vaccine
The Food and Drug Administration (FDA) is adding a label to Johnson & Johnson s COVID-19 vaccine, warning that it has been linked to rare cases of Guillain-Barré syndrome (GBS), a neurological disorder in which the body s immune system mistakenly attacks part of its nervous system.
There have been 100 preliminary reports following vaccination after approximately 12.5 million doses administered, FDA said in a statement. Of these reports, 95 of them were serious and required hospitalization. There was one reported death.