From Meryl Nass:
I checked the Federal Register and there has been no notice that Cominarty has been added to the National Childhood Vaccine injury Program (NVICP). I confirmed this by checking whether Cominarty had been added to the childhood schedule, and according to the HRSA, which manages both compensation programs, it has not.
So, if you receive the licensed Comirnaty vaccine, correctly labeled as the brand-name product and not the vaccine being fobbed off as licensed product, and you are injured, you are free to sue the manufacturer for your injury. Could this be why Pfizer wrote, “Pfizer does not plan to produce any product with these new [Comirnaty National Drug Codes] and labels over the next few months while EUA authorized product is still available and being made available for U.S. distribution.”
If, however, you receive the Pfizer-BioNTech vaccine under Emergency Use Authorization, or the Moderna or J and J vaccine, you can’t sue anyone. You have the right to beg HRSA for compensation of lost wages and unpaid medical bills, period. So far, HRSA and the Countermeasures Injury Compensation Program it administers have not paid out one dime for the approximately one million injuries and 20,000 deaths reported to VAERS for any COVID vaccine, nor a cent for any unreported injuries. In fact, they have not paid out a nickel for any injuries from any monoclonal antibodies, remdesivir, other drugs, ventilators, etc. that are all being used (a.k.a. shielded) for COVID under the EUA program.
In other words, the federal government (DHHS) has not admitted a single injury was caused by a COVID vaccine or any COVID product. CDC says it has not linked a single death to a COVID vaccine–not even when the patient walked into the vaccination center but got carried out to the morgue. FDA doesn’t know much about myocarditis, Bell’s Palsy, thrombosis, thrombocytopenia, pulmonary emboli, etc. There are no black box warnings on any of the COVID vaccines.
HRSA, FDA, CDC and NIH are all agencies within the federal Department of Health and Human Services. They have all gotten their stories straight. They know nothing and they are just following orders. This article provides examples of how each of these 4 agencies helped hide the truth, failed to carry out their public health mission, and spread false medical narratives. It made no difference which party was in power. Heil HHS!
These agencies can’t find a doggone problem in the 20 or so databases they are spending many $millions of your money to “study.”
Want to know the biggest conspiracy in the US right now? It is the HHS.
FDA has access to a bunch of electronic databases it has termed the “BEST” Initiative, and it published a plan to use them to study heart attacks, pulmonary embolism, thrombocytopenia, etc. back in July. Where are the results, FDA? What are you waiting for? (According to CDC, “More than 459 million doses of COVID-19 vaccines were administered in the United States from December 14, 2020, through November 29, 2021.”). It seems clear that we aren’t supposed to be informed of FDA’s findings until everyone possible has been vaccinated, at which point the results will be irrelevant.
In October 2020, FDA’s Steve Anderson told us there were even more databases that would be studied. And here is a more recent FDA list of the databases they are supposed to be using to assess COVID vaccine safety, in addition to VAERS, which FDA and CDC jointly share.
On August 23, 2021, FDA announced its databases were inadequate to assess myocarditis, so BioNTech would have to do it for them. Here is what FDA wrote about its inability to use VAERS and its many other databases:
- As noted above, the FDA acknowledges that “We have determined that an analysis of spontaneous postmarketing adverse events reported under section 505(k)(1) of the FDCA [in other words, VAERS–Nass] will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis.
- Furthermore, the pharmacovigilance system that FDA is required to maintain under section 505(k)(3) of the FDCA [in other words, FDA’s many other databases that cost the taxpayer zillions–Nass] is not sufficient to assess these serious risks.”
NOT SUFFICIENT????
Unsaid, but implied, is that if FDA is incapable of studying thousands of reported cases of myocarditis, it probably cannot study the other serious adverse events that have been reported in conjunction with COVID vaccines.
VAERS has operated for 30 years, collecting reports of vaccine adverse events. It averaged under 100 cases of myocarditis reported yearly until this year. Through November, CDC reports it received 1949 reports of myocarditis and pericarditis, in those under 30. CDC didn’t say what the total number of reports for all ages was.
Somehow, these HHS don’t seem all that concerned that the admitted reporting rate of myocarditis is over 20 times the average during the past 30 years. Why?
CDC has been even more shady in its analyses of safety as FDA, if that is even possible. Below, Nancy Messonier, then head of Immunizations and Respiratory Diseases at CDC, presented this list of databases that CDC would be using in the evaluation of COVID vaccine safety, on December 10, 2020. Apart from the V-safe (which they stopped talking about last January), VSD (which somehow can’t find any problems, not even myocarditis) and VAERS, all these other databases have been MIA.
NIH, whose job has never been to issue treatment guidelines, but instead to do and fund research, suddenly took over the treatment guidelines for COVID early in 2020. It formed a committee of internal and eternal “experts” to make up the guidelines. How were they chosen? That is not clear, but what is clear is that 16 of these so-called experts had current or recent financial entanglements with Gilead, the maker of remdesivir. NIH and the US Army also owned pieces of remdesivir. A number of the experts had financial conflicts with Merck. While NIH is the single biggest funder of medical research in the world, I cannot recall seeing a single study it funded on the safety of COVID vaccines. Yet somehow vaccines are its number one recommendation.
It is not even clear that the guidelines committee is functional. The NIH has been sued to learn whether a vote was even taken by the committee regarding its ivermectin guidelines, which fly in the face of the evidence on ivermectin. How was NIH somehow authorized to issue guidelines in the first place?
Here is what has obviously occurred. All these agencies were told they had to keep quiet on vaccine problems (and perhaps problems of other COVID treatments), and they had to fiddle with their data or their analytic methods, or both, to get the required results. And there was to be NO BAD NEWS, no matter what. And no good news regarding generic treatments.
As we have seen, the so-called scientists and physicians working as bureaucrats in these agencies all caved, sucked it up, did the dirty work, kept their jobs, and betrayed their oaths and the trust of the people of the USA and the world.
Meryl Nass, MD
45 Beals Ave.
Ellsworth, Maine 04605
207 412-0004 H
207 522-5229 C
merylnass@gmail.com