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Federal official: CDC, FDA taking reports of blood clots and J&J Covid-19 vaccine seriously
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Federal official: CDC, FDA taking reports of blood clots and J&J Covid-19 vaccine seriously
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A week after receiving the AstraZeneca COVID-19 vaccine, a 37-year-old woman in Norway went to the emergency department with fever and persistent headaches. A CAT scan of her head showed a blood clot in blood vessels involved in draining the brain, but her levels of platelets, involved in clotting, were low. She was treated with platelet infusions and a blood thinner, but had a bleed in her brain the next day. She underwent surgery to relieve the pressure on her brain but died two days later.
This is the side effect, known as cerebral venous sinus thrombosis, that has caused a week of worries around the COVID-19 vaccine developed by AstraZeneca. On Tuesday, the U.S. government said that it had seen the same effect six times among the 6.8 million people given a dose of a similar vaccine, from Johnson & Johnson, and that it recommended a pause on use of that vaccine out of an abundance of caution, while researchers investigated.
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Sofia Esposito is one of many Boston women watching closely for any potential issues after getting a Johnson and Johnson vaccine. I feel like I m healthy and I don t have any health condition that would interfere with that, she said. Download our mobile app for iOS or Android to get alerts for local breaking news and weather.
Johnson & Johnson s COVID vaccine was paused after six women, out of nearly 7 million people to receive the shot across the country, were diagnosed with a rare blood clotting disorder known as cerebral venous sinus thrombosis, or CVST.
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