The lead front page article in today's New York Times reports:
"A poll last month showed that only 9 percent of Americans believed drug
companies were generally honest, down from 14 percent in 2004. In contrast,
34 percent of people said they trusted banks, and 39 percent trusted
supermarkets."

"A year after Merck's withdrawal of its arthritis medicine Vioxx led to an
industrywide credibility crisis, the Food and Drug Administration is
blocking new medicines that might previously have passed muster. Doctors are
writing fewer prescriptions for antidepressants and other drugs whose safety
has been challenged, like hormone replacement therapies for women in
menopause."

"Consumers have been irritated for years by drug prices in the United
States, which are higher than in other industrialized countries. But anger
at the industry reached a new pitch in the summer of 2004, with the
disclosure that several companies had suppressed the results of clinical
trials that showed an increased risk of suicidal thoughts by people taking
antidepressants."

But the drug industry's defining spin about its fraudulent claims and
corrupt marketing practices goes to Sidney Taurel, chief executive of Eli
Lilly & Company, and former congressman, Billy Tauzin, president of the
Pharmaceutical Research and Manufacturers of America who blame the public
for "unrealistic" expectations about drugs.

Taurel: "Executives at the major drug companies say they are concerned that
consumer mistrust has led to unrealistic expectations about drug safety and
risks, stunting the development of new medicines."
Tuzin: "We've created an impression with the American public that when a
drug is approved, it's perfectly safe."

"Unrealistic" to expect safety to be the first priority in the drug
development and approval process?

"Unrealistic" to expect pharmaceutical companies not to operate like the
purveyors of snake oil who made false claims and concealed their products'
lethal side effects?

"Unrealistic " to texpect an industry that is given long-term patent
exclusivity--as no other industry recieves--would not violate the public
trust by concealing from physicians and customers lethal risks?

"Unrealistic" to expect that the FDA would not approve a medicine to be
widely marketed as "safe and effective" when it has triggered severe,
potentially lethal side effects in clinical trials?

"Untealistic" to trust that an FDA-approved medicine will not trigger
cardiac arrest, or cause liver damage, or diabetes, or mania, psychosis, and
/or violent suicidal or homicidal outbursts?

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