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(Last Updated On: July 13, 2021) The U.S. Food and Drug Administration on Monday added a warning to the fact sheet for Johnson & Johnson’s COVID-19 vaccine saying that data suggests there is an increased risk of a rare neurological disorder in the six weeks after inoculation. In a letter to the company, the FDA classified the chances of getting Guillain-Barré syndrome (GBS) after vaccination as being “very low.” Still, it said J&J vaccine recipients should seek medical attention if they have symptoms including weakness or tingling sensations, difficulty walking or difficulty with facial movements. Around 12.8 million people have received J&J’s one-dose vaccine in the United States. The FDA said 100 preliminary reports of GBS in the vaccine recipients include 95 serious cases that required hospitalization and one reported death.

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