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Abraham Flexner on staff at
the Carnegie Foundation,
and funded by the Rockefeller
Foundation, 'sourced' the American 'medical' reformation following US
Congressional acceptance of the "Flexner
Report."
This infamous treatise exclusively benefited the IG Farben/Rockefeller
petrochemical pharmaceutical alliance that vilified every form of natural
healing, replacing nutrition with
petrochemicals to monopolize
healthcare.
In her 1993 book The Molecular Vision of Life, Dr. Lily E. Kay, whom a
2001 MIT News Office obituary
referred to as "one of the
outstanding historians of biology of her generation," argued that the "new
biology" was largely forged by the Rockefeller
Foundation and its subsidiary program at the
California Institute of
Technology (Caltech) through a
consensus between a scientific elite and a business elite whose broader
aims centered on eugenics and the need to create a
mechanism of social control and
human
engineering:
"The new science did not just
evolve by natural selection of
randomly distributed disciplinary variants, nor did it ascend solely through
the compelling power of its ideas and its leaders. Rather, the rise of the new
biology was an expression of the
systematic cooperative efforts of America's scientific establishment -
scientists and their patrons - to direct
the study of animate phenomena
along selected paths toward a shared vision of science and
society." - Dr. Lily E. Kay
Practioners of
alternative healing methods
consider the application of chemical
toxins and surgeries to be 'allopathic medicine'.
"The Allopathic
approach to healing is a far cry from Hippocratic method of healing which
attempted to use natural methods to balance 'humors.'
"The term
"allopathy" was invented by German doctor Samuel Hahnemann.
He conjoined
allos "opposite" and pathos
"suffering" as a referent to harsh medical practices of his era which
included bleeding, purging, vomiting and
the administration
of highly toxic drugs.
These practices were based on the ancient
Greek humoral theory which attributed
disease to an imbalance of four humors (i.e., blood, phlegm, and black and
yellow bile) and four bodily conditions
(i.e, hot, cold, wet and dry) that
corresponded to four elements (earth,
air, fire,
and water).
Physicians following the
Hippocratic tradition attempted to
balance the humors by treating
symptoms with "opposites." - William Jarvis
Reliance on
toxic chemical drugs is
based upon the philosophy of Santorio Santorio, also known as
Sanctorius.
Santorio
argued throughout his career
that the fundamental properties of human health were
mathematical ones, such as
number,
position, and
form - breaking from
describing the body and its functions in terms of Aristotelian (and Galenic)
elements and qualities.
This radical break with
traditional medical theory
and natural philosophy proposed that the human body was
a clockwork machine the
workings of which were determined by the
shapes and positions of its
interlocking parts.
This, therefore, could be
broken down into constituent
molecules.
Beginning from a fundamentally unsound foundation
Santorio made 'phenomenal' properties, seen from
a mechanistic Newtonian viewpoint,
central to his worldview of
nature and
medicine.
While the central
metaphor of Aristotelian natural philosophy and Galenic medicine was organic,
Santorio made it mechanical: the
clock (more generally,
the machine) became the
metaphor for nature opening up a window for biochemistry and, later, molecular
biology.
While his 'trail and error' experiments were replicated and
augmented by his followers and finally surpassed by those of Antoine Lavoisier
he is still regarded by many as the father of
experimental
physiology.
"The pen is mightier than the sword.
Mightier than pen or sword is the pill."
Aldous Huxley
"How does a doctor subscribing to "first do no harm" find himself or
herself prescribing either drugs that are inherently harmful or drugs at
hazardous levels? Follow the money". - Tom Pula
"When patients ask for a drug, they tend to get the
drug regardless of whether it is appropriate for them." -
Joel Weissman, health policy expert
"According to the 2005 Partnership Attitude
Tracking Study, 40% believe that prescription medicines are
"much safer" to use than
illegal drugs.
These controlled substances are not just highly
dangerous, but they can prove lethal." -
Joseph T. Rannazzisi, May 16, 2007
1990 Americans spend $40 billion on
prescription
medications.
1998 JAMA study estimates 106,000
prescription
medications deaths.
2004
Americans spend $190 billion on prescribed
medications.
2006 Americans spend $280
billion on prescription
medication.
2009 Pharmaceutical manufacturers gain
FDA approval to distribute medical journal articles describing unapproved
off-label uses of drugs.
2011 Record 4 billion prescriptions in US
2015 Americans spend $413 billion on prescribed
drugs.
Over 1000% increase in twenty five
years.
80% of the active
pharmaceutical ingredients used to make drugs sold in America are imported and
40% of finished drugs are made in
foreign countries - much of both from China.
When designing a
chemical, the manufacturer must first decide what degree of chemical purity is
needed based on the intended use.
The following list describes the
seven most common grades for chemicals and reagents, from highest to lowest
grade/purity:
ACS grade meets or exceeds purity standards set by the
American Chemical Society (ACS). This grade is acceptable for food,
drug, or medicinal use and can be used for ACS applications or for general
procedures that require stringent quality specifications and a purity of =95%.
Reagent grade is generally equal to ACS grade (=95%) and is acceptable
for food, drug, or medicinal use and is suitable for use in many laboratory and
analytical applications.
USP grade meets or exceeds requirements of the
United States Pharmacopeia (USP). This grade is acceptable for food,
drug, or medicinal use.
United States Pharmacopeia is acceptable
for most laboratory purposes, but formulation should always be reviewed to
ensure appropriate methodology.
NF grade meets or exceeds requirements
of the National Formulary (NF).
The USP and the NF (USP– NF)
jointly publish a book of public pharmacopeial standards for chemical and
biological drug substances, dosage forms, excipients, compounded preparations,
medical devices, and dietary supplements.
Laboratory grade is
the most popular grade for use in
educational applications, but its exact levels of impurities are unknown. While
excellent for teaching and training, it is not pure enough to be offered for
food, drug, or medicinal use.
Purified grade, also called pure or
practical grade, meets no official standard; it is not pure enough to be
offered for food, drug or medicinal use of any kind.
Technical grade is
used for commercial and industrial purposes; it is not pure enough to be
offered for food, drug or medicinal use of any kind.
Of critical
importance here is the allowance of a huge amount of contaminants.
Purity of 95% with an allowance of 5% contaminants may not matter in a
variety of applications but is critical in food, drug or medicinal use of any
kind.
No manufacturer would dare to use a lower quality to increase
profit !
No lab technicians would 'accidentally' use a lower quality
grade!
"Apothecary, n. - The doctor accomplice,
undertaker benefactor and grave worm provider."
Ambrose Bierce
The US Chamber of Commerce and the
Pharmaceutical Research and Manufacturers of America ("PHRMA") argue
that exposing generic pharmaceutical manufacturers to
state law tort liability will
negatively impact the American healthcare system by denying doctors and
patients in some states access to certain generic medications.
Under
the Supremacy Clause of the
US Constitution, federal laws
represent the supreme law of the land and
may preempt or override state laws.
1984
Hatch-Waxman Act allows generic drug makers to
capture the market while bypass
testing requirements by simply claiming their generic drug is equivalent to
an approved brand-name drug
and carries the same labeling.
1992 Prescription Drug User Fee Act (PDUFA)
is marketed for its miraculous ability to reduce the time and cost of bringing
"lifesaving drugs" to market in time to save substantial numbers of 'disease'
victims.
(Choose two or more of the above to comply with
Obamacare.)
If the FDA rules a drug is safe,
even if it
kills a loved one,
(or a loved one kills you !)
you have no recourse !
"Sick days are typically unplanned, which results
in significant burdens to corporations ." - Rick Chaifetz, CEO of ComPysch
"People are being forced to chose between being
a good employee or being
a good family member" - Linda
Meric, director of 9 to 5, National Association of Working
Women
June 23, 2011 PLIVA,
Inc. v. Mensing
Federal drug regulations applicable to
generic drug manufacturers directly
conflict with, and thus preempt, state-law tort claims alleging a failure
to provide adequate warning labels.
Supreme Court holds "sameness"
requirement of Hatch-Waxman Act preempts state imposition of stricter
labeling requirements on generic drugs.
Supreme Court rules that
federal law related to pharmaceutical regulations preempts a person's ability
to sue in state courts and allege that a generic drug is poorly designed and
manufactured.
Supreme Court rules that
the FDA has authority over
pharmaceuticals.
80% of all drugs consumed in the US are, from now
on, exempt from liability for
side effects, mislabeling and
virtually any other adverse
reactions.
Generic pharmaceutical manufatures
become exempt from
multi-million dollar court-imposed settlements and
no longer have to worry about safety or
side effects awarded to victims of their generic drugs.
"Today's court
decision provides a
disincentive for generic makers of drugs to monitor safety of their
products and to make sure that they have a surveillance system in place to
detect adverse events that
pose a threat to patients." - Michael Carome, Public Citizen's Health
Research Group
June 24, 2013 Mutual
Pharmaceutical Co. v. Bartlett
Generic drug manufactures
cannot be held liable under state law for not adequately labeling medication
when federal law prohibits them from changing the label from the original brand
name drug.
Commercial messages are ingrained by
endlessly repetition.
Human aspire to be elevated
into a position outside of nature.
But many commonly prescribed
pharmaceuticals promote cancer !
Hormone replacement therapy is among the
most controversial medications.
Industrially produced estrogen can
promote uterine as well as
breast
cancer.
"Taking menopause hormones for five years doubles the risk
for breast cancer." -
Marilynn Marchione 12/13/08
Many
pharmaceuticals warn of cancer causation.
Omeprazole
(Prilosec©) causes abnormal
cell growth and stomach tumors (carcinoids) in
rats.
Spironolactone (Aldactazide©, Aldactone©) a
blood pressure medicine,
sometimes prescribed for hormonal imbalances and facial hair growth in women,
causes tumors in
rats.
Elidel© and Protopic©,
are associated with lymphoma and
skin cancer.
The rheumatoid
arthritis injections Cimzia©, Enbrel©, Humira© and
Remicade©, expensive bio-tech drugs have been associated with
lymphoma.
"In the New England Journal of Medicine,
Sept. 25, 2008, investigators noted a higher incidence of cancer in subjects
taking Vytorin©."
- Joe Graedon, pharmacologist & Teresa Graedon, nutrition
expert
"Today's announcement that the ENHANCE study failed to find any
positive benefit from the addition of Zetia® to a common, inexpensive,
generic therapy raised concerns that attempts were made to mask the minimal
value of this new drug."- Representative John Dingell, Committee on Energy
and Commerce chairman 1/15/08
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