Above chart click below for Cytochrome P450 maturation. Children do not have mature cytochrome P450 families and cannot metabolize the excipients in vaccines as neonates.Read…age of maturity of Cytochrome P450 For example:
Hep B (aluminum hydroxide, yeast protein, phosphate buffers, sodium dihydrogen phosphate dihydrate)
Vitamin K shot are given at birth
Phenol (carbolic acid – a poisonous substance derived from coal tar)
– Benzyl alcohol (preservative)
– Propylene glycol (better known as “edible” antifreeze)
At 14:00 Ben Swan shows that black boys under “36 months” (3 years) had higher autism. This goes along with the new study that shows that children under 3 do not have a mature detox mechanism (Cytochrome P450) in order to detox the excipients in vaccines such such as phenol, alcohol, polysorbate 80, formaldahyde. Aluminum & mercury inhibit Cytochrome p450. See INABILITY OF INFANTS TO METABOLIZE VACCINE EXCIPIENTS
Studies conducted over the last decade have clearly demonstrated the link between adverse reactions to Psycho-Pharmaceutical medications and underactive or underperforming CYP450 enzymes. This has caused some to wonder whether or not the recent uptick in mass shootings and the obvious link to many of the perpetrators and prescription drugs could be related to the performance of the CYP450 enzymes. Additional research, however, is now causing more questions to be asked in reference to the connections that chemicals like Glyphosate may have in the inhibition of proper CYP450 performance and, thus, in the uptick in mass shootings.
For those unfamiliar with the functions of the CYP450 enzymes, CYP450 stands for the Cytochrome P450 enzymes. Scientists understand these enzymes to be responsible for metabolizing almost half of all drugs currently on the market. P450 gene variants (polymorphisms) are implicated in the variability in drug response among a wide range of individuals. READ MORE…
Pharmacogenetics is the study of inherited genetic differences in drug metabolic pathways which can affect individual responses to drugs, both in terms of therapeutic effect as well as adverse effects.
Individual variability in drug efficacy and drug safety is a major challenge in current clinical practice, drug development, and drug regulation. For more than 5 decades, studies of pharmacogenetics have provided ample examples of causal relations between genotypes and drug response to account for phenotypic variations of clinical importance in drug therapy. The convergence of pharmacogenetics and human genomics in recent years has dramatically accelerated the discovery of new genetic variations that potentially underlie variability in drug response, giving birth to pharmacogenomics. Read ABSRACT
VLA comment: 10 % of Caucasians, for example, are unable to metabolize these modern drugs. Hence, the epidemic of suicides and homicides. Early clinical examples of genetic influence on drug response involved variations in single genes (i.e., monogenic inheritance) in which polymorphisms (no metabolic ability) of a single gene encoding a drug-metabolizing enzyme responsible for the metabolism and disposition of a substrate drug caused aberrant response to the drug.The phenotypic variation can be dramatic, especially when no alternate pathway exists to perform the same function.
VOL 48, ISSUE 3 THE LITTLE BLACK PILL (2015) LEGAL DEFENSE
Effexor and a multiple of other psyche drugs, can cause people to commit murder and proposes how an nontraditional but commonly recognized criminal defense should be applied to such people. Effexor is labeled for homicidal ideations. The rest are black box warned for suicidal ideations. But the reality is that there are two sides to the same coin. Suicide is committed by those who blame themselves. Homicide is committed by those who blame “others”. If the pharmaceuticals put homicidal ideations on each drug, as Effexor did) the public would connect the heinous murders such as school shootings with the drug. Suicides and the homicides are committed by those persons (10% of Causcasians and 7 % of African Americans) who are “non metabolizers”. These demographics, simply by genetic variations, do not have the Cytochrome P450 2D6 physiological mechanics to metabolize today’s modern psyche drugs. The drugs therefore accumulatesin the body in such a toxic manner that the distressed person either kills himself or another. Today suicides in veterans who are given drugs for PST is at an epidemic proportion.
Part III analyzes two defenses, involuntary intoxication and automatism, which a criminal
defendant taking antidepressants could raise to avoid being
After a comparison of these two defenses –
Part IV proposes that courts accept automatism as a viable defense for criminal defendants who take Effexor and then commit homicide. Automatism could function as either a complete defense (absolute exoneration) or as a partial defense (sentence mitigation). In giving life to the automatism defense, courts should consider the latest scientific findings about the link between genetic mutations and one’s inability to process drugs and the resulting toxic effect.
Genetic testing for mutations on the CYP450 gene can prevent future homicides by identifying people who are predisposed to side effects from these drugs.
INFANTS INABILITY TO METABOLIZE THE TOXIC EXCIPIENTS IN VACCINES
(click herefor studies on infant metabolism of vaccine ingredients)
More and more research in the area of pharmacogenetics is being funded by pharmacuetical companies in order to give physicians better guidelines for dosages.
Cytochrome P450, the major detox mechanism in the body (plants, animals and humans), varies among individuals. Individuals can be rapid metabolizers, normal metabolizers and poor or non metabolizers.
Other than the fact that 10% of Caucasians and 7% of African Americans are straight out “non-metabolizers” and have the tendency to suicidal and/or homicidal ideations when given prescription drugs, cytochrome P450 is “maturing” and all infants do not have full mature activity this important detox mechanism until the age of 3.
At birth and one hour old, all infants, except those whose parents have declined, will received a Vitamin K shot and Heb B vaccination. With this they will be injected at birth with 450 mcgs. of aluminum and an amount of formaldehyde…we are talking an hour old.
According to Dr. Sherri Tenpenny:
Dr. Sherri J. Tenpenny’s Integrative Medical Center, by the time a child has reached 5 years of age, he or she has been injected with a total of 1,795 micrograms (mcg), or 1.795 milligrams of formaldehyde, as follows Read more…
Hepatitis b – 3 doses x 15 mcg each
DTaP – 5 doses x 100 mcg each
Polio (IPV) – 5 doses x 200 mcg each
Influenza – 6 doses x 25 mcg each
Hepatitis A – 1 dose x 100 mcg each
Total: 1,795 mcgs of fomaldehyde by age five
Included in the list of vaccine excipients is not only formaldehyde but ethanol, phenol, polysorbate 80,benzethonium chloride,glutaraldehyde, acetone, thimerosal, aluminum. All needing mature cytochrome P450 enzymes to metabolize.
VLA Comment: Finally we have proof that our infants and children are being directly injected with poisons (toxins) that cannot be metabolized at such a young age.
Lets look more closely at the excipient ingredients in vaccines. The following understanding that Infants cannot metabolize the multiple overload of the repetitive excipeint ingredients in multiple vaccines due to an inability of infants and children to metabolize these toxins due to the generally recognized fact that Cytochrome P450 is “immature” in infants and children.
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: 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 Study…. http://www.ncbi.nlm.nih.gov/pubmed/17468864 Some manufacturers of GSE have stated that their extract has compounds nearly identical to benzethonium chloride
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
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.
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.
Psychiatric drugs are now being given to infants and toddlers in unprecedented numbers.
An analysis of 2013 IMS Data, found that over 274,000 infants (0-1 year olds) and some 370,000 toddlers (1-3 years age) in the U.S. were on antianxiety (e.g. Xanax) and antidepressant (e.g. Prozac) drugs. This report also found over 1,400 infants were on ADHD drugs.
A 2014 Georgia Medicaid analyses led by Susanna Visser at the CDC (see a video of her fascinating talk) when extrapolated nationwide by the New York Times found that over 10,000 toddlers were put on ADHD treatments. (Dr. Visser is currently working on national estimates but believes that the estimate from the Georgia data is conservative.) READ MORE…