Since the dawn of humanity, people have sought treatments
for disease and ways to improve their health. The earliest medical
caregivers were probably little more than tribal elders who used their
knowledge and experience with indigenous plants to help their communities.
Today's medical caregivers must understand and apply a vast array
of scientific, psychological, legal and medical knowledge in a highly-regulated
environment. Huge pharmaceutical corporations provide a stunning variety
of medications, every one scientifically validated safe and effective
- at least until recently. |
Before 1820, medicine in the United States was a haphazard
environment. Medical caregivers often had little formal training and
few of the instruments and drugs that practitioners of medicine today
find essential. Medicine was basically a folk practice, characterized
by chaotic educational processes such as apprenticeships. Doctors
exhibited the same widespread ignorance of biology, pathology, pharmacology,
and science as the general population. Before laws that governed doctors
and prescriptions, unregulated drug manufacturers made immense fortunes
selling (sometimes addictive) products with little or no proven effectiveness
to uninformed customers.
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Humans' fear of death and desire for maximum health
drove many consumers to knowingly purchase ineffective products, regardless
of price. Pharmaceutical companies realized incredible profits and
power with such products, benefiting from the lack of effectiveness
testing and the lack of laws to prevent exploitation of desperate
consumers. Abuses of the public trust and the public health in the
past eventually led to laws, regulations and federal oversight to
prevent such exploitation and fraud. |
Perhaps nothing is more representative of the practice
of 20th century medicine in the United States than the professional
certification of physicians and pharmacists. Treatments are now scientifically
verified and medications are clinically tested for safety and effectiveness.
It wasn't kindly drug manufacturers that accomplished these foundations
of modern medical care. Instead, it was a horrific tragedy with unregulated
medications (contaminated pertussis vaccine that caused the death
of thirteen children in St Louis) that forced politicians to turn
to science as the foundation of laws regulating the distribution and
sale of medications. |
Recent lobbying, pressure from campaign donors, and
the return of antiquated laws have threatened the resurgence of some
detrimental conditions once relegated to history books, including
the ability of corporations to reap huge profits from the sale of
unsafe medications. |
Drug manufacturers often shower politicians with "donations"
(once called bribes) to obtain favorable legislation. "Fast track"
licensing and failure to disclose data from other studies have allowed
the entry of pharmaceuticals such as Vioxx into the market. The Medicare
program inexplicably prohibits the government from negotiating for
lower prices from drug manufacturers. Despite almost 100 years of
successful regulation of the American medical and pharmaceutical professions,
it now seems that the United States has returned to the 19th century,
when fantastic profits were more important than protecting the public
from unfair pricing and unsafe medications. |
Every successful technology in modern society is the
result of careful scientific or engineering analysis. The scientific
processes that made the manufacturers of drugs such as Vioxx aware
of negative side effects in internal studies also uncovered those
same side effects once the medications were in distribution. Because
science provides such safeguards by exposing harmful side effects,
your pharmacy continues to be a place where you can spend your money
relatively confident that the product you are purchasing is safe
and effective.
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