Amount of aluminum adjuavnt in vaccines per dose

Pneumococcal vaccine 0.125 mg
• Diphtheria-tetanus-pertussis (DTaP) vaccine– 0.17-0.625 mg
• Haemophilus influenzae type b (Hib) vaccine– 0.225 mg
• Hib/Hep B vaccine 0.225 mg
• Hep A vaccine (for children) 0.225-0.25 mg
• Hepatitis B vaccine (Hep B) 0.225-0.5 mg
• Hep A/ Hep B vaccine 0.45 mg
• DTaP/inactivated polio/ Hep B vaccine 0.85 mg
• DTaP/inactivated polio/Hib vaccine 0.33 mg
• Human Papillomavirus (HPV) vaccine 0.225 mg-0.500 mg

TOXIC INGREDIENTS FOUND IN VACCINES

aluminum hydroxide
aluminum phosphate
ammonium sulfate
amphotericin B
animal tissues: pig blood, horse blood, rabbit brain, dog kidney, monkey kidney, chick embryo, chicken egg, duck egg, calf (bovine) serum
betapropiolactone
fetal bovine serum
formaldehyde
formalin
gelatin
glycerol
human diploid cells (originating from human aborted fetal tissue)
hydrolized gelatin
mercury thimerosol (thimerosal, Merthiolate)
monosodium glutamate (MSG)
neomycin
neomycin sulfate
phenol red indicator
phenoxyethanol (antifreeze)
potassiumdiphosphate
potassium monophosphate
polymyxin B
polysorbate 20
polysorbate 80
porcine (pig) pancreatichydrolysate of casein
residual MRC5 proteins
sorbitol
tri(n)butylphosphate
VERO cells, a continuous line of monkey kidney cells
washed sheep red blood

Vaccine Ingredients and Manufacturer Information
(alphabetical order by vaccine)

https://vaccines.procon.org/view.resource.php?resourceID=005206

Vaccine Excipient & Media Summary
Excipients Included in U.S. Vaccines, by Vaccine

https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf

UK Study: Brains Of Children With Autism Are Loaded With Aluminium

“Age-Specific and Cumulative Aluminum Exposure by 18 Months of Age

Birth 250 mcg aluminum
2 months 1225 mcg aluminum
4 months 975 mcg aluminum
6 months 1000 mcg aluminum
12 months 600 mcg aluminum
15 months 623 mcg aluminum
18 months 250 mcg aluminum”

As you can see, a baby receives a total of 4,925 mcgs of aluminum by the time they are 18 months of age, from vaccinations alone.

Read more:
http://www.exposingworldgovernment.com/…/uk-study-brains-o…/

http://www.exposingworldgovernment.com/2017/12/10/uk-study-brains-of-children-with-autism-are-loaded-with-aluminium/

New Study Indicates that Widespread Exposure to Aluminum Is Setting the Stage for Catastrophic Neurological Damage
http://vaccineimpact.com/…/study-record-levels-of-aluminum…/

http://vaccineimpact.com/2017/study-record-levels-of-aluminum-found-in-autistic-children-brain-tissue/

High Levels of Aluminum Found in Autistic Children's Brain Tissue

http://www.dirtybigpharmatruth.com/high-levels-of-aluminum-found-in-autistic-childrens-brain-tissue.html

The First 6 Years Of A Fully Vaccinated Child’s Life Looks Like This…

17,500 mcg 2-phenoxyethanol (antifreeze)
5,700 mcg aluminum (neurotoxin)
Unknown amounts of fetal bovin serum(aborted cow blood)
801.6 mcg formaldehyde (carcinogen, embalming agent)
23,250 mcg gelatin (ground up animal carcuses)
500 mcg human albumin (human blood)
760 mcg of monosodium L-glutamate (causes obesity & diabetis)
Unknown amounts of MRC-5 cells (aborted human babies)
Over 10 mcg neomycin (antibiotic)
Over 0.075 mcg polymyxin B (antibiotic)
Over 560 mcg polysorbate 80 (carcinogen)
116 mcg potassium chloride (used in lethal injection)
188 mcg potassium phosphate (liquid fertilizer agent)
260 mcg sodium bicarbonate (baking soda)
70 mcg sodium borate (Borax, used for cockroach control)
54,100 mcg of sodium chloride (table salt)
Unknown amounts of sodium citrate (food additive)
Unknown amounts of sodium hydroxide (Danger! Corrosive)
2,800 mcg sodium phosphate (toxic to any organism)
Unknown amounts of sodium phosphate monobasic monohydrate (toxic to any organism)
32,000 mcg sorbitol (Not to be injected)
0.6 mcg streptomycin (antibiotic)
Over 40,000 mcg sucrose (cane sugar)
35,000 mcg yeast protein (fungus)
5,000 mcg urea (metabolic waste from human urine)

How many of these ingredients are on the Prop 65 list?

http://vaxxter.com/the-first-6-years-of-a-fully-vaccinated-childs-life-looks-like-this/

Polysorbate 80 in vaccines as well helps open the blood/brain barrier making it easier for toxic metals in vaccines and as well inflammation causing aluminum adjuvants and other metals to pass through.

Big Pharma’s Dirty Little Secret: Vaccine-Induced Autoimmune Injury

https://www.healthnutnews.com/big-pharmas-dirty-little-secret-vaccine-induced-autoimmune-injury/

Nanoparticles enhance brain delivery of blood–brain barrier-impermeable probes for in vivo optical and magnetic resonance imaging

Abstract
Several imaging modalities are suitable for in vivo molecular neuroimaging, but the blood–brain barrier (BBB) limits their utility by preventing brain delivery of most targeted molecular probes. We prepared biodegradable nanocarrier systems made up of poly(n-butyl cyanoacrylate) dextran polymers coated with polysorbate 80 (PBCA nanoparticles) to deliver BBB-impermeable molecular imaging probes into the brain for targeted molecular neuroimaging. We demonstrate that PBCA nanoparticles allow in vivo targeting of BBB-impermeable contrast agents and staining reagents for electron microscopy, optical imaging (multiphoton), and whole brain magnetic resonance imaging (MRI), facilitating molecular studies ranging from individual synapses to the entire brain. PBCA nanoparticles can deliver BBB-impermeable targeted fluorophores of a wide range of sizes: from 500-Da targeted polar molecules to 150,000-Da tagged immunoglobulins into the brain of living mice. The utility of this approach is demonstrated by (i) development of a “Nissl stain” contrast agent for cellular imaging, (ii) visualization of amyloid plaques in vivo in a mouse model of Alzheimer's disease using (traditionally) non–BBB-permeable reagents that detect plaques, and (iii) delivery of gadolinium-based contrast agents into the brain of mice for in vivo whole brain MRI. Four-dimensional real-time two-photon and MR imaging reveal that brain penetration of PBCA nanoparticles occurs rapidly with a time constant of ∼18 min. PBCA nanoparticles do not induce nonspecific BBB disruption, but collaborate with plasma apolipoprotein E to facilitate BBB crossing. Collectively, these findings highlight the potential of using biodegradable nanocarrier systems to deliver BBB-impermeable targeted molecular probes into the brain for diagnostic neuroimaging.

http://www.pnas.org/content/108/46/18837.full

Polysorbate 80: A Risky Vaccine Ingredient (lots of direct info)

https://healthimpactnews.com/2016/polysorbate-80-a-risky-vaccine-ingredient/

Why wasn't this important study in any of pharma journal, or the study ever addressed at the CDC?

Food Chem Toxicol. 1993 Mar;31(3):183-90.
Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats.

Gajdová M1, Jakubovsky J, Války J.

Abstract
Neonatal female rats were injected ip (0.1 ml/rat) with Tween 80 in 1, 5 or 10% aqueous solution on days 4-7 after birth. Treatment with Tween 80 accelerated maturation, prolonged the oestrus cycle, and induced persistent vaginal oestrus. The relative weight of the uterus and ovaries was decreased relative to the untreated controls. Squamous cell metaplasia of the epithelial lining of the uterus and cytological changes in the uterus were indicative of chronic oestrogenic stimulation. Ovaries were without corpora lutea, and had degenerative follicles.

https://www.ncbi.nlm.nih.gov/pubmed/8473002?dopt=Abstract

Concerns on Using Polysorbate 80 in Vaccines

Immunocontraceptive

Here’s a strange one -

A patent for a vaccine that would decrease the ability for fertility in animals (which can be found here -submitted by the University
of Georgia Research Foundation) “preferably includes Tween 80 (Polysobate 80)”. [3]

The patent immediately goes on to site the book “The Theory and Practical Application of Adjuvants” after declaring Tween 80 as a preferable ingredient. This book lists the benefits and pitfalls associated with the use of different adjuvants. Studies include such problems as isolation, adverse reactions and practical applications.[3][4]

At least there is a practical application for it - decreasing fertility?!

Read more:
http://blindedbythelightt.blogspot.com/.../concerns-on...

1. (WO1999034825) FERTILITY IMPAIRING VACCINE AND METHOD OF USE

https://patentscope.wipo.int/search/en/detail.jsf?docId=WO1999034825

Aluminum - The Unapproved Toxin in Vaccines aluminum adjuvants, several of the vaccines included on the adolescent vaccine checklist include aluminum. The new Gardasil 9 vaccine, for instance, has 500 mcg of aluminum in each of the two doses. The vaccines for hepatitis and meningococcal Group B also contain aluminum adjuvants, as does the Tdap booster shot. While these ingredients are listed on the FDA website, information distributed to patients often does not include this. New formula of the HPV vaccine, Gardasil 9, has more than DOUBLE THE AMOUNT OF ALUMINUM ADJUVANT
in each dose than the previous formula New formula of the HPV vaccine, Gardasil 9, has more than DOUBLE THE AMOUNT OF ALUMINUM ADJUVANT in each dose than the previous formula Aluminum, in any amount, is a known toxin that has been proven to cross the blood-brain barrier and to be linked to autoimmune diseases in prone individuals. Currently, there is no testing to determine which children may be prone to acquiring Autoimmune Syndrome Induced by Adjuvant (ASIA) or at what levels or frequency of exposure to aluminum in vaccines this may occur. While there are currently no clinically approved.

Old Formula
(Gardasil)
New Formula
(Gardasil 9)
225mcg Aluminum adjuvant/dose
2-3 recommended doses
Total Aluminum exposure = 650 - 825mcg

New Formula
(Gardasil 9)
225mcg Aluminum adjuvant/dose
2-3 recommended doses
Total Aluminum exposure = 650 - 825mcg
500mcg Aluminum adjuvant/dose
2-3 recommended doses
Total Aluminum exposure = 1000 - 1500mcg

Both meningococcal and HPV vaccines are recommended by the CDC, but during the trials, Menactra (one of the major meningococcal vaccines) and Gardasil were never evaluated for safety when both were given simultaneously. The National Vaccine Information Center conducted their own research and discovered an increased risk of certain serious side effects. When Gardasil and Menactra were given to a patient on the same day: Respiratory problem reports increased by 114 percent Cardiac problem reports increased by 118 percent Neuromuscular and coordination problem reports increased by 234 percent Convulsions and central nervous system problem reports increased by 301 percent Reports of injuries from falls after unconsciousness increased by 674 percent.

http://info.cmsri.org/…/Teenage%20Immunization%20Journal-Fi…

https://vactruth.com/2017/08/21/refusal-to-vaccinate-form/
Why You Should Never Sign the Refusal to Vaccinate Form

http://info.cmsri.org/the-driven-researcher-blog/vaccinated-vs.-unvaccinated-guess-who-is-sicker
Vaccinated vs. Unvaccinated: Mawson Homeschooled Study Reveals Who is Sicker


https://vactruth.com/2016/11/17/aluminium-adjuvants-not-approved/
Aluminium Adjuvants Have Never Been Approved For Use In Vaccination

https://disqus.com/by/lowellhubbs/comments/
New Research Proves Brains of Children with Autism are Loaded with Aluminum

https://vactruth.com/2017/12/05/aluminum-and-autism/
New Research Proves Brains of Children with Autism are Loaded with Aluminum

https://cdn2.hubspot.net/hubfs/519118/Content%20Offerings/Teenage%20Immunization%20Journal.pdf

Front Neurol. 2015; 6: 4.
Published online 2015 Feb 5.
PMCID: PMC4318414
Biopersistence and Brain Translocation of Aluminum Adjuvants of Vaccines
Romain Kroum Gherardi,1,* Housam Eidi,1 Guillemette Crépeaux,1 François Jerome Authier,1 and Josette Cadusseau1

1Faculté de Médecine and Faculté des Sciences et Technologie, INSERM U955 Team 10, Université Paris Est-Créteil, Créteil, France
Edited by: Lucija Tomljenovic, University of British Columbia, Canada

Reviewed by: Samir Kumar-Singh, Antwerp University, Belgium; Mark P. Burns, Georgetown University Medical Center, USA; Lucija Tomljenovic, University of British Columbia, Canada
*Correspondence: Romain Kroum Gherardi, Faculté de Médecine and Faculté des Sciences et Technologie, INSERM U955 Team 10, Université Paris Est-Créteil, 8 rue du Général Sarrail, Créteil 9410, France

Abstract
Aluminum oxyhydroxide (alum) is a crystalline compound widely used as an immunological adjuvant of vaccines. Concerns linked to the use of alum particles emerged following recognition of their causative role in the so-called macrophagic myofasciitis (MMF) lesion detected in patients with myalgic encephalomyelitis/chronic fatigue/syndrome. MMF revealed an unexpectedly long-lasting biopersistence of alum within immune cells in presumably susceptible individuals, stressing the previous fundamental misconception of its biodisposition. We previously showed that poorly biodegradable aluminum-coated particles injected into muscle are promptly phagocytosed in muscle and the draining lymph nodes, and can disseminate within phagocytic cells throughout the body and slowly accumulate in brain. This strongly suggests that long-term adjuvant biopersistence within phagocytic cells is a prerequisite for slow brain translocation and delayed neurotoxicity. The understanding of basic mechanisms of particle biopersistence and brain translocation represents a major health challenge, since it could help to define susceptibility factors to develop chronic neurotoxic damage. Biopersistence of alum may be linked to its lysosome-destabilizing effect, which is likely due to direct crystal-induced rupture of phagolysosomal membranes. Macrophages that continuously perceive foreign particles in their cytosol will likely reiterate, with variable interindividual efficiency, a dedicated form of autophagy (xenophagy) until they dispose of alien materials. Successful compartmentalization of particles within double membrane autophagosomes and subsequent fusion with repaired and re-acidified lysosomes will expose alum to lysosomal acidic pH, the sole factor that can solubilize alum particles. Brain translocation of alum particles is linked to a Trojan horse mechanism previously described for infectious particles (HIV, HCV), that obeys to CCL2, signaling the major inflammatory monocyte chemoattractant.

Full study:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318414/…

Harmful Ingredients in Vaccines

http://dangersofvaccines.com/harmful-ingredients-vaccines/

Vaccine Ingredients - How Vaccines Are Made - Which Ingredients Are the Most Toxic

http://www.drgreenmom.com/vaccines/vaccine-ingredients/

More bad news, vaccines found additionally to be contaminated with various other toxic metals.

Dirty Vaccines: New Study Reveals Prevalence of Contaminants

http://info.cmsri.org/the-driven-researcher-blog/dirty-vaccines-new-study-reveals-prevalence-of-contaminants

Dirty Vaccines – Part Two: What the Industry Knows and Isn't Telling You

http://www.greenmedinfo.com/blog/dirty-vaccines-part-two-what-industry-knows-and-isnt-telling-you


http://info.cmsri.org/the-driven-researcher-blog/dirty-vaccines-new-study-reveals-prevalence-of-contaminants

Little Things Matter: The Impact of Toxins on the Developing Brain
Canadian Environmental Health Atlas

We’ve been studying the impact of toxins on children for the past 30 years and reached the inescapable conclusion: little things matter. We’ve discovered that extremely low levels of toxins can impact brain development. We have also discovered that subtle shifts in the intellectual abilities of individual children have a big impact on the number of children in a population that are challenged or gifted. Steps should be taken to reduce children's exposure to toxins or suspected toxins. You can read more about how toxins impact brain development and the supportive documentation for this video here:

https://www.youtube.com/watch?v=E6KoMAbz1Bw

This is just the tip of the iceberg as to existing information, and as well in regard to the applicable scientific studies showing that the aluminum adjuvants in vaccines, are not safe.