This Article from Trial Site may require a Subscription. These authors have proposed a “New” Disease Category with the acronym pCoVS

Here is the executive summary

The Smoking Syringe: Was evidence withheld from ACIP when they recommended the Pfizer-Vaccine?

Opinion Editorial by: David Wiseman Ph.D., M.R.Pharm.S.

Summary
On Monday, August 30, 2021, the Advisory Committee on Immunization Practices (ACIP) voted unanimously to approve a recommendation that stated:

The Pfizer-BioNTech Covid-19 vaccine is recommended for people 16 years of age and older under FDA’s Biologics License Application (BLA) approval

This recommendation was quickly endorsed by CDC Director, Dr. Rochelle Walensky.

In approving this recommendation, ACIP heard evidence from Pfizer, Kaiser Permanente, CDC, and other scientists on the safety and effectiveness of the vaccine.
Apparently fully or partially absent from this evidence were six studies, cited in a post-vote presentation. These studies, including those by CDC and Pfizer scientists, describe waning vaccine effectiveness, or effectiveness against the delta strain, from the 90-95% range to, in one case to as low as 42%.
The inclusion of these missing studies would have yielded a different risk-benefit analysis.
Given the ramifications this recommendation is already having on vaccine mandate policy, the evidence presented to ACIP does not appear to meet the highest level of standards for scientific integrity and conduct.
Other intense safety signals, such as a 177 times increase in the number of deaths per vaccinated person reported for Covid-19 vaccines, compared with flu vaccines, were not considered.
ACIP did not consider the possible effects of the vaccines on pregnancy or the reproductive system, hinted at by the announcement the same day by NIH, to fund studies on the links between the Covid-19 vaccines and menstrual disorders.
ACIP did not consider other possible long-term effects (cancer, autoimmune disease) of the vaccines related to their falling under the FDA classification of a “gene therapy product,” and made no comment about the lack of studies performed by Pfizer/BioNTech “for the potential to cause carcinogenicity, genotoxicity, or impairment of male fertility.”
The significant short and potentially long-term cardiac, vascular, hematological, musculoskeletal, intestinal, respiratory or neurologic symptoms health issues stemming from the use of these vaccines pose a major and expensive public health problem.To concretize recognition of, and to spur action to avert and confront this potential public health crisis, we have proposed the term:
Post Covid Vaccine Syndrome – pCoVS

There needs to be:
Assignment of ICD10 and related tracking or reimbursement codes for pCoVS.
Funding for research and tracking for long-term and delayed pCoVS.
Regulation of the Pfizer, Moderna, and Janssen vaccines as Gene Therapy products, requiring long-term follow-up.
Since FDA and CDC cannot assure us about the safety of two vaccine doses, how can they give any assurance about a third (or more doses)?

Article is Entitled : THE SMOKING SYRINGE , WAS EVIDENCE WITHELD FROM ACIP BEFORE PFIZER APPROVAL ?

https://trialsitenews.com/the-smoking-syringe-was-evidence-withheld-from-acip-when-they-recommended-the-pfizer-vaccine/

Fully’s Comment : This New Disease is destined to become THE most prevalent disease in the coming years BUT it is 100% Preventable ….DON’T GET THE JAB !

Alas 2 Billion have already been Jabbed. But don’t worry hang in there Big Pharm will create a new Jab that will Counter this one and you shall be saved…..Lets call it The Anti Vaxx Vaccine