Citizens Petition the FDA on Aluminum Adjuvents
In May of 2021, Dr. Christopher Exley petitioned the Department of Health and Human Services of the Food and Drug Administration for administrative action to ensure accurately reported and consistent levels of Aluminum in all vaccines.
Dr. Exley gives his official comment on the petition:
Professor Exley’s comment to his petition to the FDA Agency: FOOD AND DRUG ADMINISTRATION
Document Type: Other Title: Citizen Petition from Siri & Glimstad, LLP
Document ID: FDA-2021-P-0433-0001
Comment: Once these data on the aluminum content of infant vaccines were known to me I asked myself about their absolute significance.
What were the data witnessing? Sloppy processing by manufacturers? If so then why weren’t these issues flagged up by internal auditing of the products?
Do manufacturers not actually measure the final content of aluminum in their vaccines? It looks that way. If they do not are they still assuming that the information they give on the patient information leaflet is accurate?
Presumably they are as this amount of aluminum per dose of vaccine has been extensively researched and optimized by the manufacturer to give the antibody titre necessary for the vaccine to be effective.
Since the vaccine is wholly ineffective in the absence of the aluminum adjuvant, then the amount of aluminum adjuvant injected into the infant must be tightly controlled in providing a safe and effective vaccine. Isn’t that correct?
How can vaccine manufacturers be so complacent about such a critical issue? Is there a darker side to all of this? It may or it may not be true that manufacturers carefully optimize the aluminum content of infant vaccines.
However, how often do manufacturers monitor the efficacy of their vaccine in receiving infants?
How do they know that the data they must have for their clinical trials is reproduced in real time vaccinations in infants.
Simply, how do they know that their vaccine works against its target disease? Do they even care?
These data on the aluminum content of infant vaccines suggest very strongly that from the moment the vaccine is aliquoted to its vial ready for subsequent administration to an infant the manufacturer has no interest in whether it is either effective or safe. No one is monitoring the former and vaccine manufacturers have no responsibility for the latter.
Vaccine manufacturers are businesses first and foremost, it is not up to them to make sure that their products are safe and effective. It is the responsibility of the FDA and the FDA is clearly neglecting this responsibility as is the European Medicines Agency.
A cartel of neglect and complacency that puts infants all of the world at risk, not only from the disease the vaccine is meant to be effective against but critically from the injection of an unknown amount of a known neurotoxin into vulnerable infants.
What can you do?
Of 13 infant vaccines tested, only 3 had the correct amount of aluminum as listed by the manufacturer.
Ask your pediatrician if your baby’s vaccine is on the list.
You can read the vaccine report on aluminum content of infant vaccines and print out the list for your pediatrician or OBGYN.
https://www.sciencedirect.com/science/article/pii/S0946672X21000523
