Europe Puts Serious Neurological Defect As Possible Side Effect Of Johnson’s Vaccine | health | Essential information for better health | DW



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The drug regulator in Europe said today, Thursday (July 22, 2021) that it has added a rare neurological disorder known as Guillain-Barré syndrome as a possible side effect of the Johnson & Johnson vaccine against Covid-19, after examining 108 registered cases worldwide.

The European Medicines Agency (EMA) said: “After evaluating the available data, the safety committee concluded that there may be an association between Johnson & Johnson’s vaccine to prevent Covid-19 disease and Guillain-Barré syndrome. “

The same agency said last May that it was examining reports of a rare disorder of nervous disorders in people who have received anti-Covid-19 doses of AstraZeneca, at a time when authorities around the world are seeking transparency on the safety of coronavirus vaccines.

Guillain-Barré syndrome is a rare neurological disease in which the body’s immune system attacks the protective sheath of nerve fibers. Most of these cases occur after a microbial or viral infection.

According to the Mayo Clinic website, the first symptoms of this syndrome are weakness and numbness in the extremities, and these symptoms can spread to the whole body, which can lead to paralysis and should be urgently transferred to the hospital.

And the United States Food and Drug Administration warned of the syndrome after taking the Johnson-and-Johnson vaccine, and reported a few days ago that there were at least 100 people infected with it on more than 12.5 million who received this vaccine, and one of the infected died.

Johnson & Johnson said earlier that “the chances of this happening are very low and the rate of reported cases is only slightly above the base rate for the general population.”

In its warning, the United States Food and Drug Administration said that in the vast majority of people who developed the syndrome, symptoms began to appear within 42 days of receiving the vaccine.

AA / AH (Reuters)



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