Congress Receives Vaccine Safety Project Details Including Actions Needed for Sound Science and Transparency

By Unattributed | World Mercury Project

World Mercury Project Note: Last week, 15 dedicated children’s health and medical choice advocates joined Robert F. Kennedy, Jr. on Capitol Hill to fulfill our promise to the community to provide crucial vaccine safety information to every member of Congress. Meetings with Congressional Members, Senators, and staff took place over a four-day time period to explain WMP’s six-step Vaccine Safety Project that details the actions necessary to introduce sound science and transparency to our vaccination program. Federally elected officials can no longer ignore the chronic health conditions—tied in no small part to adverse vaccine reactions—that currently affect over half of our nation’s children. Not only are these officials now aware of the conflicts of interest and inadequate science upon which the vaccine program is built, but they have been given a common-sense plan for enacting desperately needed changes that puts children’s health first.
By the World Mercury Project Team

The long-term health effects of our vaccine program are inadequately studied and our regulatory bodies are conflicted. Childhood health epidemics have mushroomed along with the childhood vaccine schedule.


Vaccines contain many ingredients, some of which are known to be neurotoxic, carcinogenic and cause autoimmunity. Vaccines injuries can and do happen. The National Vaccine Injury Compensation Program of Health and Human Services (HHS) has awarded almost $4 billion for vaccine injuries since 1988.

Common sense dictates that these actions must be taken:

  1. Subject vaccines to a scientifically rigorous approval process.
  2. Require reporting of vaccine adverse events. Automate Vaccine Adverse Event Reporting System (VAERS) and Vaccine Safety Datalink(VSD) databases for research.
  3. Ensure all parties involved with federal vaccine approvals and recommendations are free from conflicts of interest.
  4. Reevaluate all vaccines recommended by the Advisory Committee on Immunization Practices (ACIP) prior to the adoption of evidence-based guidelines.
  5. Study what makes some individuals more susceptible to vaccine injury.
  6. Support fully-informed consent and individual rights to refuse vaccination.

The Six Steps to Vaccine Safety

The details regarding each of the six steps to vaccine safety were discussed with members of Congress, Senators and staff to help them understand why they must act now to stop the childhood epidemics.

#1: Subject vaccines to a scientifically rigorous approval.

  • Vaccines are regulated by the FDA’s Center for Biologics Evaluation and Research (CBER) division as “biologics” and are not always put through the same level of safety testing as new pharmaceuticals, which are regulated under the Center for Drug Evaluation and Research (CDER.)
  • Vaccines, which are given to healthy patients, should be tested more rigorously than drugs because they are not given to treat an existing disease.
  • Inadequate testing currently ensures that the true risk/benefit assessments for the safety and cost of vaccines are impossible to calculate accurately.
  • These vaccines are given to about 4 million American infants annually.

#2: Require reporting of vaccine adverse events. Automate Vaccine Adverse Event Reporting System (VAERS) and Vaccine Safety Datalink(VSD) databases for research.

Reporting and study of adverse events after receipt of vaccines is currently haphazard and antiquated. Since these two databases are the primary sources of U.S. post-licensure surveillance, serious side effects of vaccination that were unclear or not seen in clinical trials will be missed.

The VAERS is the online system into which doctors and patients report adverse events after vaccination. HHS admits that the system likely records only about 1% of the actual adverse events but even after a three-year HHS/Agency for Healthcare Research and Quality (AHRQ) study showed the feasibility of automating reports using electronic medical records, Centers for Disease Control (CDC) has been non-responsive to “multiple requests to proceed with testing and evaluation.”

  • Clinical trials for vaccines typically only enroll a few thousand patients in total. When vaccines are subsequently approved for use in populations of millions of healthy individuals, it is imperative that rates of known adverse events and any new or rare adverse events are monitored.
  • Without adequate safety follow-up, serious side effects may be missed entirely putting the public at risk (examples of the past importance of safety follow-up include hormone replacement therapy, Vioxx and amphetamines).
  • There has never been a comparative study of broad health outcomes in vaccinated vs. unvaccinated populations.

The National Childhood Vaccine Injury Act (NCVIA) requires healthcare providers to report:


  • Any adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine; or
  • Any adverse event listed in the VAERS Table of Reportable Events Following Vaccination that occurs within the specified time period after vaccination.

But, in practice, this doesn’t happen. There is no consequence for failing to report an injury. There is no mechanism for prosecution of non-compliance and, therefore, no incentive for a busy doctor to report vaccine safety problems.

The VSD is a collaborative project between CDC’s Immunization Safety Office and eight private health care organizations. The VSD was started in 1990 to monitor safety of vaccines and conduct studies about rare and serious adverse events following immunization. However, research is currently hampered by lack of broad access to this publicly-funded database, variability of reporting and the statistical structure of the database.

#3: Ensure all parties involved with federal vaccine approvals and recommendations are free from conflicts of interest.

FDA’s Vaccine and Related Biological Products Advisory Committee (VRBPAC) is responsible for licensing vaccines. CDC’s Advisory Committee on Immunization Practices (ACIP) is responsible for adding vaccines to the recommended schedules.

  • CDC or NIH Employees whose names appear on vaccine patents can receive up to $150k in licensing fees per year (in perpetuity).
  • Regarding VRBAC, a House OGR Committee Report found that the “overwhelming majority of members, both voting members and consultants have substantial ties to the pharmaceutical industry,” and “committee members with substantial ties to pharmaceutical companies have been given waivers to participate in committee proceedings.”
  • A similar report on the ACIP found that, “The CDC grants blanket waivers to the ACIP members each year that allow them to deliberate on any subject, regardless of their conflicts, for the entire year.”

A 2009 HHS Office of the Inspector General report found that:

  • “CDC had a systemic lack of oversight of the ethics program.”
  • 97 percent of committee members’ conflict disclosures had omissions.
  • 58 percent had at least one unidentified potential conflict.
  • 32 percent had at least one conflict that remained unresolved.
  • CDC continued to grant broad waivers to members with conflicts.

All vaccine regulatory agencies must rigorously enforce their ethics policies to ensure that our vaccine program is free from financial conflicts of interest.

#4 Reevaluate all vaccines recommended by the Advisory Committee on Immunization Practices (ACIP) prior to the adoption of evidence-based guidelines.

A yes vote by ACIP results in:

  • Mandating the vaccine to millions of children.
  • Immunity from liability for the manufacturers.
  • Inclusion in the Vaccines for Children program.

However, prior to 2012, ACIP did not use evidence-based guidelines to evaluate their vaccine recommendations. Evidence Based Practice is “the conscientious, explicit and judicious use of current best evidence in making decisions about the care of the individual patient. It means integrating individual clinical expertise with the best available external clinical evidence from systematic research.” The final ACIP guidelines published in November of 2013 outlined clearly, for the first time, a standardized plan to evaluate the quality and strength of the research behind each recommendation for a vaccine for each population. ACIP’s recommendations include the populations, timing, spacing, number of doses, boosters and appropriate ages for each vaccine to be administered.

The CDC’s infant schedule, given to approximately 4 million babies a year, was largely adopted before these guidelines were in place. Vaccines recommended before the adoption of evidence-based guidelines should not have been “grandfathered” in. Earlier ACIP recommendations should be thoroughly reviewed in light of the new guidelines and current research.

#5 Study what makes some individuals more susceptible to vaccine injury.

The Institute of Medicine (now National Academy of Medicine) has issued three disturbing reports on the evidence for suspected and/or reported vaccine adverse events.

For 80% of the suspected vaccine adverse conditions investigated, there wasn’t enough research evidence to accept or reject vaccine causation. Of the reviews with sufficient evidence, 72% found that the vaccine did likely cause the injury.

In 2013, the IOM studied the entire Childhood Immunization Schedule and stated:

“No studies have compared the differences in health outcomes… between entirely unimmunized populations of children and fully immunized children… Furthermore, studies designed to examine the long-term effects of the cumulative number of vaccines or other aspects of the immunization schedule have not been conducted.”

The Vaccine Injury Compensation Program has paid out over $3.8 billion in compensation to victims of vaccine injury. The children and adults who have been compensated for injuries have never been studied to determine why they were injured, in an effort to make vaccines safer for everyone. Preventing vaccine injuries should be tackled as zealously as we tackle preventing infectious diseases.

Vaccine safety science, particularly long-term safety science, is inadequate to ensure children’s safety or to accurately assess risks for purposes of informed consent.

#6 Support fully-informed consent and individual rights to refuse vaccination.

The American Academy of Pediatrics statement on the ethics of informed consent includes the following stipulation, “patients should have explanations, in understandable language, of …; the existence and nature of the risks involved; and the existence, potential benefits, and risks of recommended alternative treatments (including the choice of no treatment).”

In the case of vaccination, informed consent is often ignored completely in real world settings.

By law, all health care providers in the United States who administer, to any child or adult, any of the following vaccines – diphtheria, tetanus, pertussis, measles, mumps, rubella, polio, hepatitis A, hepatitis B, Haemophilus influenzae type b (Hib), influenza, pneumococcal conjugate, meningococcal, rotavirus, human papillomavirus (HPV), or varicella (chickenpox) – shall, prior to administration of each dose of the vaccine, provide a copy to keep of the relevant current edition vaccine information materials that have been produced by the Centers for Disease Control and Prevention (CDC) to the parent or legal representative of any child to whom the provider intends to administer such vaccine, or to any adult to whom the provider intends to administer such vaccine.”

In practice, particularly when multiple vaccines are administered on the same day, many parents report that they received the Vaccine Information Sheet (VIS) as they left and there was no explanation of information before a vaccine was given. It is also rare that medical history is thoroughly discussed to identify contraindications to a vaccine. For example, a patient with a family history of autoimmunity is likely at increased risk for an autoimmune reaction after vaccination.

The following are examples of the types of information that patients may learn after the fact from the Vaccine Information Sheets:

  • “Severe events have very rarely been reported following MMR vaccination, and might also happen after MMRV. These include: Deafness, long-term seizures, coma, lowered consciousness, brain damage.”
  • Or this from the Polio VIS and several others: “As with any medicine, there is a very remote chance of a vaccine causing a serious injury or death.”

Lack of informed consent encompasses vaccine advertising as well. While television drug ads disclose the side effect risks of that drug at length, vaccine advertising does not. The patient, again, is at a disadvantage.

[Read more here]

Robert O’Leary, JD BARA, has had an abiding interest in alternative health products & modalities since the early 1970’s & he has seen how they have made people go from lacking health to vibrant health. He became an attorney, singer-songwriter, martial artist & father along the way and brings that experience to his practice as a BioAcoustic Soundhealth Practitioner, under the tutelage of the award-winning founder of BioAcoustic Biology, Sharry Edwards, whose Institute of BioAcoustic Biology has now been serving clients for 30 years with a non-invasive & safe integrative modality that supports the body’s ability to self-heal using the power of the human voice. Robert brings this modality to serve clients in Greater Springfield (MA), New England. Robert can be reached at romayasoundhealthandbeauty@gmail.com.

 

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