If Drug Test Volunteers Test Positive for Either of the Two Genetic cytochrome P450 “Detox” Pathways, that Exist in HALF THE POPULATION, Which Keep them from Processing the Drug and Being Poisoned, THEY ARE EXCLUDED FROM THE TRIAL!

“Prior to all drug trials with human subjects, every participant is tested for specific pharmacogenetics to determine if they have either of the two genetic variants that are prevalent in 50% of the entire population that impair their ability to process a pharmaceutical medication via their cytochrome P450 detoxification pathways, hence poisoning them if they take it.

All volunteers that test for either of these two genetic variants ARE EXCLUDED FROM THE TRIALS! No one given a standard ‘once size fits all, trial and error” pharmaceutical medication is tested for these common variants prior to prescribing! This Connecticut child may have had one of these two variants and could have been under the affects of pharmaceutical poisoning!

As they say, “BINGO!”

This standard *TRIAL AND ERROR’ medical community practice kills over 764,000 people including children every year!

In addition to a better attitude toward our own defense, “We need to call for coverage of this pharmacogenetic testing prior to ALL prescriptions!!!!!

www.HealthandDna.com
“This is a very clear way to stop this MADNESS… We all know why patients are NOT PRETESTED, NOW WE NEED TO DEMAND EVERYONE IS!!!
http://youscript.com/healthcare-professionals/what-is-youscript/pharmacogenetic-testing/

PHARMACOGENETIC TESTING

”Pharmacogenetic testing is the alternative to “one size fits all:and :trial and error” prescribing. Knowledge of patient drug metabolizing gene variants ”found in more than half of patients”can help determine the appropriateness and dosage of many of the most commonly prescribed drugs,”

ADVERSE DRUG REACTIONS “ADRs: A serious medical problem

”In 2000, Genelex began offering physicians an alternative to the one size fits all and trial and error prescribing of drugs. All too often, a serious Adverse Drug Reaction (ADR) is the result (of one size prescribing).:ADRs are not medical errors, but events that occur in spite of compliance with dosage recommendations. A 1998 meta-analysis of 39 prospective studies in US hospitals estimated that 106,000 Americans die annually from ADRs. (JAMA, 279;1200 1998) Adverse drug events are also common (50 per 1,000 person years) among ambulatory patients, particularly the elderly on multiple medications. The 38% of events classified as serious are also the most preventable. (JAMA, 289;1107 2003)”

In Light,
Donna