The Food Pharmacy instructs Pfiza and Moderna to expand their warning labels. Corona 19 Venue Mainly cited the results of research and new institutional data published last year for the risk of heart damage side effects related to MRNA shots related to teenagers and young people.
spirits Comirnaty Vaccine and modern Spikevax vaccine.
Both vaccine A warning about the risk of heart side effects, which the doctor calls the heart muscle inflammation (inflammation of the heart muscles) and the heart (inflammation of the membrane surrounding the heart), was generally higher within the first week after vaccination. Previous labels were designated between 18 and 24 years old for Moderna vaccines and 12-17 years old for pureizers, but new warnings apply to men between 16 and 25 years old for two vaccines.
The FDA said, “After administering 2023-2024 MRNA COVID-19 vaccine formula, the highest estimated incidence of myocarditis and/or pericarditis is in men between 16 and 25 years of age.
According to the FDA, the percentage of myocarditis and pericarditis is about eight cases per million for children and adults under 65 years old, the FDA said.
The new warning ordered by the FDA added at 38 percentage per 1 million people.
Disease Control and Prevention Center I explained before Covid-19 Vaccine ratio of rare myocarditis and pericardritis.
A CDC official told the vaccine advisors of the agency. transmission After vaccination, acute myocarditis said, “It tends to be resolved quickly, and the risk has not increased in recent season data between 12 and 39 years of age.
It is not clear whether Pfizer or Moderna has filed an objection. They had “within 30 days of this letter” to refute demand. The spokesman for Moderna and Pfizer did not immediately respond to the request.
“Americans deserve a radical transparency on the safety and efficacy of the covid vaccine, and the FDA conveys a promise to do so. Moderna and PFIZER must take action to recognize the side effects of Covid vaccine, which leads to cardinomyitis and coreitis.” Nixon did not explain why it was posted for more than a month after the letter was written.
They appeared before the FDA’s website. hearing Republican-led Senate Security and Government Committee were organized by the Government Affairs Committee on how the health authorities are forced to force and hide and hide myocarditis and other side effects related to the covid-199 vaccines.
Aaron Siri, Health and Human Services, a lawyer who worked closely with Minister Robert F. Kennedy Jr. In the past During the transition, it is one of the witnesses to ask the FDA to candidates for Covid-19 and other vaccines and veterinarians.
The FDA said the warning was deprived of the new data and results of the agency’s safety monitoring system. october From scientists with people who developed Covid-19-related cardinomyitis.
The story of this kind of seat labeling began with many people who are familiar with the situation by Dr. Peter Marks, the former highest vaccine official of the FDA, but that the public officials have not been completed yet. Mark left the FDA April 5th.
Scientists of this study were followed by people who faced blood pain and those who faced the amount of troponic in the blood. They were mainly young men.
Scientists wrote in this study by FDA officials, “Their clinical process has almost always had a low range of prevalence and heart dysfunction, but myocardial injuries were common.”
As explained by the study, the FDA’s new warning showed that the discovery of heart MRI showed “improvement over the time of most people.”
The FDA said, “It is not known whether these heart MRI results can predict the long-term heart effect of myocardial salts.
