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The FDA’s main warning about Pfizer when the reaction to the vaccine is being closely monitored

The FDA recently acknowledged that there is a great interest in another Pfizer product. It is now issuing warnings about a type of anti-inflammatory treatment called JAK inhibitors.

“The US health regulator has added the strictest warning to the label of Pfizer drugs, Eli Lilly and AbbVie belong to a class of anti-inflammatory treatments known as JAK inhibitors, citing the risk of problems. serious health problems and death in patients 50 years of age and older,” Reuters reported on Friday, citing the drug’s makers.

“The addition warning on the label following an agency review of Pfizer’s Xeljanz after initial results from a trial in February showed an increased risk of serious heart-related problems and cancer in some patients undergoing treatment. drug therapy,” the report added.

The alarming development is a reminder of Pfizer’s rushed approval of “vaccines”. In June, the COVID-19 Vaccine Safety Engineering Working Group (VaST) noted an adverse reaction in vaccinated males between the ages of 16 and 24. The development of a cardiac condition has been reported. observed in adolescents and young adults and was significantly higher after the second dose in men.

Representative Thomas Massie noted that the Expected and Observed categories in VAERS differed significantly for Myocarditis and Pericarditis in the 12 to 49 age groups.

A retired cardiac surgeon recently circulated a warning with the AHA that markers of heart inflammation are increasing sharply in patients with increasing rates of Covid mRNA vaccination.

The warning for the AHA is clear: “Patients have a 1 in 4 risk of serious problems after vaccination, compared with 1 in 9 before.”

The controversial memo, a call for more research, has sparked a backlash among institutions trying to control the story. But it has more endorsements than the mainstream media allows.

One Scientific publications organized by NIH explored a potential relationship between the mRNA ‘vaccine’ and reports of heart inflammation in July 2021.

“As of June 26, 2021, a total of 322 million doses of the vaccine have been administered, and to date, 79 children aged 16 to 17 years and 196 young adults aged 18–24 years have been confirmed by CDC is myocarditis/pericarditis. after vaccination with COVID-19 mRNA following data analysis in VAERS,” the paper pointed out.

“Advised risk ratio for myocarditis and pericarditis events in children and young adults aged 16 to 24 years has been determined to be 0.94 (95% CI 0.59–20). 1.52). Therefore, the US FDA has added warnings about the risk of myositis and pericarditis to the COVID-19 mRNA vaccine fact sheet.”

The article continued: “Recently, the US military reported 23 patients out of 2.8 million doses of the COVID-19 mRNA vaccine administered. “Although the number of cases of myocarditis observed was small, the number of male members of the military following the second dose of the vaccine was higher than expected.”

“In a report by the Israeli Ministry of Health, every 3,000 to one in 6000 males aged 16-24 years old who received the COVID mRNA vaccine developed myocarditis and pericarditis,” it added. “90% of cases in Israel appear to be male. Although the prevalence of myocarditis in this population is high, post-vaccination rates appear to be 5–25 times higher than baseline. ”

“The European Medicines Agency also recently reported that myocarditis and pericarditis can occur in very rare cases after vaccination with COVID-19 Comirnaty. [Pfizer-BioNTech] and Spikevax [Moderna].

“The Committee therefore recommends listing myocarditis and pericarditis as new adverse events in the product information for these vaccines, along with warning to raise awareness among healthcare professionals and people using these vaccines,” the article notes. “The European Medicines Agency (PRAC) Safety Committee included 145 cases of myocarditis in the European Economic Area (EEA) among people receiving Comirnaty and 19 cases following Spikevax use. . As of May 31, 2021, approximately 177 million doses of Comirnaty and 20 million doses of Spikevax had been provided in the EEA. As of the end of May 2021, the incidence of myocarditis was 1 part per million for both Comirnaty and Spikevax in the EEA. ”

As a result, the data raises questions about whether the CDC and FDA are being upfront with Americans about real side effects, even when it’s recommended that children under 5 be vaccinated. Indeed, President Biden promised that he would everything in his power to make sure even children under 5 years old get their mRNA injection.

In 2009, Pfizer had to pay a large sum of money for the fraudulent marketing of one of its drugs.

“Pharmaceutical giant Pfizer has agreed to pay $2.3 billion to settle civil and criminal charges that it illegally marketed the now-recalled painkiller Bextra,” the New York Times said. report.

The Times noted: “This is the largest healthcare fraud settlement and largest criminal fine ever.

https://smartzune.com/the-fda-slaps-major-warning-about-pfizer-drug-as-vaccine-reactions-come-under-scrutiny/ The FDA’s main warning about Pfizer when the reaction to the vaccine is being closely monitored

Huynh Nguyen

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