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Throughout the Pandemic of Covid, people have turned to disease control and prevention centers (CDC) for safety advice. Meanwhile, Food and Drug Administration (FDA) has helped Americans trustvaccines that the organization has judged safe and effective. Now, the two trusted agencies have come together to publish a statement recommending a break in the administration of a Covid vaccine. Read on to see why the CDC and the FDA suggest a temporary stop and for more side effects of vaccine,Moderna provoked this reaction in 82% of people, the new study says.

After six reports from a rare blood clot in people who received the Johnson & Johnson vaccine, the CDC and the FDA published a joint statement that declaredThey recommend an immediate break In the use of Johnson & Johnson vaccine with abundance of caution. " The statement published on April 13 announced that the recommended break will be in place until the end of the CDC and the FDA. Investigate the situation fully. The CDC will convene with the Vaccination Practices Advisory Committee (ACIP) on April 14 to review these cases and assess their importance. Then the FDA will review this analysis and conduct an investigation into their own. Depending on what these investigations discover, the Johnson & Johnson break will be adjourned or put in place.

"At the moment, these adverse events seem extremely rare. Covid-19 vaccine safety is an absolute priority for the federal government and we take all health problem reports as a result of CVIV-19 vaccination very seriously" , said the statement. And for more vaccine guidance,Make sure you do this in the day after your Covid vaccine, let's say.

There were six cases reported from a blood clot called brain venous vinosis thrombosis (CVST) in combination with low levels of blood platelets (thrombocytopenia). The six of these cases were among women aged 18 to 48 years. The administration pause is part of "ensuring that the health care provider community is aware of the potential of these adverse events and can plan appropriate recognition and management because of the single. Required treatment with this type of blood clot, "says the statement.

The treatment of this type of blood clot is different from the treatment that would generally be administered for a blood clot. According to the declaration, "generally an anticoagulant drug called heparin is used to treat blood clots. In this context, the administration of heparin can be dangerous and alternative treatments must be given." And for more on life afterwards, discoverThe 2 places, Dr. Faisci will still not go after vaccination.

Although the possibility of experimenting CVST is frightening, experts want to remind you that it is an extremely rare event. "HisA very rare event. You are talking about one per million, and when you give millions of vaccine doses, you will see events like this you could not see in the clinical trial simply because you have not had millions of registrants, "Carlos del Rio, MD, Executive Associate Dean of the Emory University Medicine School at the Grady Health System, CNN said on April 13.

Although it is rare, del Rio said he thinks that vaccination pause is the right move until the experts understand what's going on and how to move forward. He congratulated the agencies for the priority of vaccine safety. "I want to congratulate the CDC and the FDA jumping very quickly on it, stop the vaccinations until we know more, and really trying to understand what is happening," added del Rio. And for more than New Covid vaccine news delivered directly to your inbox,Sign up for our daily newsletter.

According to the declaration, the symptoms of the CVST and thrombocytopenia began to appear within six to 13 days after vaccination among women who experienced them. The declaration exhorts the "people who have received the J & J vaccine that develop serious headaches, abdominal pain, leg pain or shortness of breath in the three weeks after vaccination" to contact their care provider immediately. health. And for more vaccine efficiency,This vaccine can protect you from all variants, a new study says.

Del Rio told CNN that blood coagulation could be due to the fact that Johnson & Johnson vaccine is a vector vaccine of adenovirus, identical to Astrazeneca. While the AstraZeneca vaccine is not approved in the United States, it has been authorized in more than 70 countries. Astrazeneca has also led to a small number of unusual blood clots with low blood platelets. The European Medicines Agency recently decided that these events should simply be listed as a "very rare side effect" of the vaccine, according to CNN. They decided that the benefits of shooting are worth the risk, but people noted should seek signs of clots. Pfizer and Moderna are mRNA vaccines, which use a different mechanism to protect you from COVID. And for more on the future of vaccination,How long is the Moderna vaccine really protects you, a new study says.