VACCINE Excipients and Cyp P450: Common excipients in Vaccines inhibit Cytochrome P450,the major detox mechanism in humans, plants and animals. Considering Cyp 450 is immature in the infant and child, the following excipients can’t be dealt with, released or detoxified in the infant and growing child. It is to be noted that the inhibition of Cytochrome P450 and the inability to release the toxins from the body in cases of Adults cause serious psychotic events including suicide and “heinous” homicides. Could these vaccine ingredients that are not metabolized by infants and children in various degrees appear like “mental illness”, hence the DSM misdiagnosis criteria?
The sample list of excipients below commonly injected MANY times into infants in many overlapping vaccines need Cyp 450 to metabolize yet some children, due to genetic variation, are totally missing the activity of Cyp 450 and, in any case all children have immature Cyp 450 activity. This may give us one of the answers to the apparent range of vaccine injury in the general population.
Re: Polysorbate 80, a common vaccine excipient:
The results indicate that these non-ionic surfactants are in vitro inhibitors of CYP-mediated metabolism
RE: Ethanol and Formaldehyde, vaccine excipients:
Re: Alcohol, a vaccine excipient
RE: Benzethonium Chloride, a vaccine excipient
Notice that in the latest drug commercials they advertiser warns against Grapefruit seed extract. This is because GSE inhibits Cytochrome P450 and therefore inhibits detoxifcation of toxic elements
Some manufacturers of GSE have stated that their extract has compounds nearly identical to benzethonium chloride
Asthma, Allergies, Inflammation & the role of Cyp 450
Re: Aluminum Hydroxide adjuvant
Is Aluminum Hydroxide inhibiting the already immature activity of Cyp 450 that apparently is important in reducing inflammation?
Cyp 450 and lungs
Aluminum Phosphate, a vaccine excipient and SHAKING BABY SYNDROME
Shaking Baby Syndrome & bone breaking symptoms:
Aluminum accumulation in bone has become much less frequent with cessation of use of aluminum-containing phosphate binders. Unfortunately, the binders which have largely replaced aluminum have not proven completely satisfactory
Osteomalacia – Mayo Clinic http://www.mayoclinic.org/diseases-conditions/osteomalacia/basics/definitio…
Osteomalacia refers to a softening of your bones, often caused by a vitamin D deficiency. Soft bones are more likely to bow and fracture than are harder, healthy bones. Note: As per the SBS & bone breaking symptom in the above link Aluminum – containing phosphae binders cause Osteomalacia as well.
The Journal of Pediatric Pharmacology and Therapeutics
“Developmental Pharmacokinetics in Pediatric Populations”
Hong Lu, PhD and Sara Rosenbaum, PhD
*Ped cyp enzymes (see graph) (very important study of the immaturity of cyp 450 superfamilies in infants and children. Synopsis: Infants do not have a mature liver or liver enzyme function such as Cytochrome P450 and its various metabolites until the age of three years old. Hence upwards of 36 vaccine doses by 18 months old containing the above excipients are poisoning the world’s emerging humanity. DOWNLOAD STUDY
The graph in the above link shows that infants and children have immature enyzmes and therefore an inability to metabolize toxins. Although these and other studies are being done so that the pharmacuetical industry can adjust dosage of pharmacuetical drugs to infants, toddlers and children, we must look at it from the point of view that the excipients in the vaccines need mature enyzmes to metabolize. This entire post lists some studies involving the need for mature enzymes in order to metabolize such ingredients as aluminum, mercury, phenol, formaldahyde, ethanol, phenol, polysorbate 80, etc. If these enzymes are not mature until the age of three years old, then by giving vaccines and moreover, multiple vaccines at one time, we are POISONING our infants and children.
Immaturity of Cyp 450 in infants (So why are we giving Hep B with
at one hour old?) Attached
Comment Hep B contains many of these excipient ingredients which an infant is unable to metabolize. This is a point that can be made when writing a model Hep B bill.
SUPER CYP 450 DATA BANK:
SuperCYP (http://bioinformatics.charite.de/supercyp) is a comprehensive resource focused on CYPs and drug metabolism.
Finally, it must be noted that non metabolism (polymorphism of cyp 450 aka lack of activity) runs in the family.
Parents and siblings will all be found to have the same polymorphism.
In addition to the MTHFR gene, there is a gene called the CYP450 pathway which is critical for effective detoxification. It is suppressed genetically in 43% of Africans. Unfortunately, CYP450 pathway affects the safety and efficacy of 90% of therapeutic drugs and other environmental chemicals.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868406/ http://www.ncbi.nlm.nih.gov/pubmed/23641907 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1390790/ http://www.biomedcentral.com/1471-2156/14/34
Furthermore, Latinos have a suppressed CYP3A4*10 enzyme and CYP3A4*16A enzyme.
“A new study published in the journal Vaccine has brought to light an extremely disturbing though still virtually unreported dark side to immunization campaigns within low-income countries, namely, the observation that infant mortality sometimes increases when the number of co-administered vaccines increases; a finding diametrically opposed to the widely held belief that vaccination is always a life-saving intervention, and that the more vaccines administered to infants the better. Read more…
Study: Neil Z Miller and Gary S Goldman Infant mortality rates regressed against number of vaccine doses routinely given: Is there a biochemical or synergistic toxicity?