Monday, January 16, 2023

Medical researcher Calls for Withdrawal of Pfizer, Moderna COVID-19 Vaccines Following New Research

An American doctor is joining the calls for the withdrawal of the messenger RNA COVID-19 vaccines, pointing to new research that highlights a connection between the shots and adverse events.

Dr. Joseph Fraiman, a doctor based in Louisiana who also conducts research on COVID-19 and other health issues, says it’s time to halt the administration of the Pfizer and Moderna COVID-19 vaccines until new clinical trials prove the benefits from the vaccines outweigh the harms.

The new research, including a reanalysis of the trials for the vaccines, raise concerns about whether the benefits from the vaccines outweigh the harms, according to the doctor.

“I don’t see how anyone couldn’t be certain that the benefits are outweighing the harms on a population level, or even in the high-risk groups. I don’t see the evidence to support that claim,” Fraiman told The Epoch Times. “But I also can’t say that there’s evidence to support that it’s potentially more harmful, but there’s also uncertainty here. … Given that scenario, I believe that people should not be given the [vaccines] outside of a clinical trial, because we need to figure out … if their benefits outweigh harm or if harm outweighs benefits.”

“The only thing that can answer that question is going to be a randomized trial,” he added.

Pfizer and Moderna did not respond to requests for comment.

The U.S. Food and Drug Administration (FDA), which cleared the shots and has never stopped promoting them, did not return an inquiry.

The Data

Fraiman led a study that reanalyzed the original Pfizer and Moderna trials. He and his colleagues concluded in a study published following peer review that the vaccinated were at higher risk of serious adverse events.

That’s one data point. Another is the identification of safety signals, or adverse events, that are potentially caused by the vaccines but require further study. The FDA revealed in December 2022 that the Pfizer vaccine was linked to blood clotting in elderly individuals. The U.S. Centers for Disease Control and Prevention (CDC), which recommends the vaccines for virtually all Americans, found hundreds of other signals in its research, according to records obtained by The Epoch Times.

Several serious problems that can lead to death have been causally linked, or proven to be caused by the vaccines. They include myocarditis, or heart inflammation.

While U.S. health officials have repeatedly downplayed the severity of myocarditis and a related condition, pericarditis, German researchers who dug into the deaths of 25 people who died suddenly at home after vaccination ruled out every potential cause except for vaccination for five of the people. They reported their results in a study that was published after peer review in late 2022.

“Given alternative causes are unlikely to cause myocarditis within one week of vaccination, this is essentially conclusive evidence that we’re seeing sudden cardiac deaths from the vaccines,” Fraiman said.

Fraiman also noted that excess mortality, or deaths from all causes, have risen during the pandemic—with spikes correlating with the introduction of the vaccines. Vaccines may not have caused the additional deaths, he says, but some researchers, including British professors Norman Fenton and Martin Neil, have examined the data and found a signal that the vaccines were linked to at least some of the excess deaths. U.S. officials say some of the deaths may be from COVID-19.

Initial Thoughts

When the vaccines were first introduced, Fraiman backed giving them to the elderly and others at high risk from COVID-19, or people of all ages with serious underlying health conditions. He says he also did not recommend against vaccination for any ages, though he told younger family members he was not sure if it was a good idea to get a jab.

Fraiman also says the vaccines likely reduced hospitalizations in the first two quarters of 2021, recalling how he did not see a single vaccinated person in his hospital until June of that year.

When he and the other scientists discovered the vaccinated were at higher risk of serious problems, he shifted to a stance of the harms likely outweighing the benefits among healthy people.

With the new evidence of harm, along with Omicron being less dangerous and more likely to evade vaccine immunity, Fraiman questions whether the benefits outweigh the serious harms even among the elderly and otherwise infirm.

“I see the likelihood that the harm could outweigh the benefit in the group who stood to benefit the most from the vaccine,” he said.

Standards Fall

Clinical trial data on the vaccines have been hard to come by, especially trials not run by the vaccine makers themselves, and the standards for the trials have been lowered over time.

The FDA authorized shots for children based on immunobridging, or trial data that found the vaccines triggered a similar antibody response in kids than that in adults. For the new bivalent boosters, created because the original vaccines have been providing much lower levels of protection against Omicron and its subvariants, no clinical data, not even antibody measurements, was provided at all. Months later, that data is still not available to the public.

Some observational studies have estimated the boosters provide subpar protection against infection and solid protection, at least initially, against hospitalization. Randomized, controlled trials are typically considered superior.

Fraiman recommends withdrawing the vaccines and U.S. officials going to the vaccine makers and asking them to demonstrate the benefits outweigh the harms in light of the changed dynamics of the pandemic. The trials should feature investigators looking closely at each COVID-19 hospitalization to distinguish whether they were caused by COVID-19, or the COVID-19 diagnosis was incidental. That distinction is known widely as being hospitalized, or dying, with COVID-19 versus from COVID-19.

The trial would take five or six months, similar to the original ones, Fraiman says.

Other Calls

Some countries, such as Denmark, meanwhile, have stopped offering booster shots to certain segments of the population. A growing number of experts, meanwhile, are calling for the administration of the Moderna and Pfizer shots, which are by far the most administered in the United States, to be halted.

The group includes Dr. Aseem Malhotra, a British doctor who turned against the vaccines in 2022 due to the growing evidence of side effects. Malhotra’s citations included the Moderna and Pfizer trials, which showed no reduction in mortality or severe disease, and the research led by Fraiman.

Linda Wastila, director of policy and research of the Peter Lamy Center for Drug Therapy and Aging at the University of Maryland, said she agrees with Fraiman, pointing to the research as well as data from the Vaccine Adverse Event Reporting System. Reports of thousands of post-vaccination deaths have been lodged with the system, in addition to hundreds of thousands of injuries.

“I’m a data scientist, and I’m overwhelmed by the congruence of all these data coming together so rapidly, all painting a horrific picture of vaccine harms that really cannot be ignored,” Wastila told The Epoch Times via email.

Wastila called for the removal of the vaccines from the market immediately, at least until safety signals identified by the CDC and FDA are closely studied.

“In not doing so, FDA and the rest of government agencies pushing these products are not only placing millions at risk for injury or death, they also are successfully encouraging rapid distrust of the institutions that are supposed to protect us,” she said.

There are other experts, such as Florida Surgeon General Dr. Joseph Ladapo, who have recommended against certain populations getting vaccinated, such as healthy young men, because they’re at higher risk of one or more side effects and stand to gain little benefit against a disease that already poses minimal risk to them. Still, other experts continue to back the vaccination of virtually all people, including Dr. Ashish Jha, coordinator of the White House COVID-19 response.


Oh, So That’s What Moderna Forgot to Tell Us About Their COVID Vaccine

The more we learn about these COVID vaccines, the more I sort of regret getting the vaccine. I already survived the virus pre-vaccine, but still got vaccinated and boosted. I’m shocked that I haven’t had a cardiac event, given how scores of young people are “dying suddenly.” I’ll have more about that later, but the death rates for young Americans have spiked, and there may be some inquiries into how these vaccines might be a factor.

Today, we’re going to piggyback off something our friends at RedState touched upon concerning Moderna not being forthcoming about some data about the vaccine. Information about the reinfection rate was buried, and an FDA panel member is not too pleased about that development. What’s even more surprising is that CNN is the outlet who reported on the incomplete disclosure of Moderna’s vaccine:

“I was angry to find out that there was data that was relevant to our decision that we didn’t get to see,” said Dr. Paul Offit, a member of the Vaccines and Related Biological Products Advisory Committee, a group of external advisers that helps the FDA make vaccine decisions. “Decisions that are made for the public have to be made based on all available information – not just some information, but all information.”

At a meeting of this FDA advisory group in June and a meeting in September of a panel that advises the US Centers for Disease Control and Prevention, the experts were presented with reams of information indicating that the new vaccine worked better than the one already on shelves, according to a review of videos and transcripts of those meetings and slide presentations made by Moderna, CDC and FDA officials.

That data – called immunogenicity data – was based on blood work done on study participants to assess how well each vaccine elicited antibodies that fight off the Omicron strain of the virus that causes Covid-19.

The data that was not presented to the experts looked at actual infections: who caught Covid-19 and who did not.

Streiff adds:

There are a few observations that can be made here. First, omitting critical data to the FDA advisory committee isn’t an oversight. Moderna’s team either knew the proposed vaccine had nearly double the current vaccine and deliberately didn’t flag that data, or they are idiots. It isn’t easy to come up with other alternatives.

The reason they did it is pretty simple. Money.

And let’s not forget that these pharmaceutical companies have full immunity from legal action. These companies can get a legal shield, but there shouldn’t be the same protections for the gun industry which has enemies at the gates looking to litigate them into extinction. They didn’t disclose all the data over money and for the sheer fact that no legal fallout could ever occur. I’m sadly not shocked there was a failure to disclose all the data before the political class, Fauci, and the Democrats forced this down our throats by threatening our employment.




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