| June 01,
2005
Mainstream media reveals the truth about the "business with
disease."
Recently, the mainstream media has
finally started unveiling the truth about the danger of pharmaceutical drugs
and "business with disease" that brings billion of dollars to the pharma industry,
and no cure to the terminally ill patients. Over a decade ago, Dr. Rath's began
his crusade against the largest and most profitable industry on earth - the
pharmaceutical industry. By lecturing in many countries around the globe he
has initiated the awareness course of action about the industry that "grows
like cancer at the expense of people."
Every year, millions of people "voluntarily" pay trillions of dollars to the
pharmaceutical industry for drugs that do not cure and often harm. Dr. Rath
has been tirelessly on the forefront of exposing the profiteering motivations
of the pharmaceutical industry and also has exposed the shoddy "science" practices
that drug companies use in developing their drugs. There is no doubt that Dr.
Rath's voice and strong appeals have been heard, and today many news organizations
are publishing stories that give extra validation to his statements.
On June
1, 2005, on the Lou Dobbs show on CNN, during a segment called "Dangerous Drugs"
the guest of the program, Congressman Ed Markey of Massachusetts, openly called
drug companies and the FDA "a conspiracy of silence." He said that "many drug
companies are abusing the FDA's accelerated approval program for drugs that
treat life-threatening diseases and drug makers are failing to conduct vital
follow-up study on the drugs after they hit the market".
The following is a
transcript of the segment from the June 1, 2005 Lou Dobbs show on "Dangerous
Drugs."
ANNOUNCER: News, debate and opinion continues. Sitting in for Lou Dobbs
is Kitty Pilgrim.
PILGRIM: Well, my next guest is taking on drug companies and
the FDA for what he calls a conspiracy of silence. Congressman Ed Markey of
Massachusetts says many drug companies are abusing the FDA's accelerated approval
program for drugs that treat life-threatening diseases. And he says drug makers
are failing to conduct vital follow-up study on the drugs after they hit the
market.
And Congressman Markey has just released an extensive report detailing
the charges and he joins me now.
And thanks for being here.
REP. ED MARKEY (D),
MASSACHUSETTS: Thank you for having me in.
PILGRIM: Let's clear this up. These
are drugs that were basically put through quickly so that they could save lives.
And the FDA requires additional testing to make sure they're OK. They're not
doing the additional testing, that's what you found in many cases.
MARKEY: That's
right. So, in other words, because the drug is so important, because it can
save lives, they go right around the regulatory process. They're approved quickly,
but with safety and effectiveness tests which have yet to be completed.
The
drug company promises that they will complete the tests. But what I found in
looking at FDA records is that drug companies go three, four, five, six, seven
years, sometimes, before they actually finish all of these safety and effectiveness
tests. Meanwhile, patients and doctors are using these drugs without knowing
whether or not, in fact, they have passed these exams.
PILGRIM: There are some
startling statistics that you've turned up: 42 of the -- 42 of the drugs that
were required by the FDA to have follow-up testing, 42 of 91 did not since is
the 1992. That's a good percentage, and yet many people, I'm sure, are quite
happy to get the drugs if they are in a life-threatening illness.
I was particularly
struck by the -- an example of a lung cancer drug that, of course, you would
want immediately if you could get it, and yet later testing proved that it had
absolutely no effect whatsoever, potentially harmless. Why would that be a problem?
MARKEY: It would be a problem because people, in many instances, because they
know they have these illnesses, will pay anything and they should know as soon
as possible that the drug is not effective, because then they, with their physician,
might be able to construct some other strategy. But the patient has a right
to know that the drug is not effective, and as soon as possible. Here, what
we're finding is that these safety and effectiveness tests are not completed
for years after approval has been given.
PILGRIM: Yes, in this case, it was
$1,800 a month for this particular drug, and they could be taking something
else. That's the other point, isn't it?
MARKEY: They could be taking something
else, and moreover, there is no requirement by the FDA that this conditional
approval be put on the label. In other words, the doctor and the patient aren't
even told on the label that it's a conditional approval. The doctor or the patient
would have to go to the FDA website, the drug company website, to find that
out but they wouldn't see it, obviously, when they were purchasing the drug
or consuming it on a daily basis.
PILGRIM: Now, the FDA, we did speak to them.
They say they closely monitor the process and in some cases the additional trials
can take years to complete, so that's what they are saying about this when we
spoke to them today. But, you're saying there is a way to fix this and you're
suggesting alternate labeling, that you have a label on the drug that says accelerated
approval. Do you think that would clear things up or would that just confuse
issues?
MARKEY: Well, I think that if each patient and physician understood
that the approval for the drug was only conditional, not permanent, that that
would put real pressure on the FDA and the drug company to complete all of the
tests as quickly as possible.
And, secondly, I also propose that there be fines
which are possible to be imposed by the FDA on the drug company. In other words,
right now the drug company keeps it on the market because the FDA doesn't have
the nerve to take it off the market because it could be life-saving. But there
is no penalty if the drug company drags its feet in conducting these tests.
PILGRIM: Well, we certainly applaud your efforts, and thanks very much for explaining
them to us, tonight, Congressman Ed Markey. Thank you.
MARKEY: Thank you for
having me on.
Above excerpt reprinted
from CNN.com © 2005 Cable News Network LP, LLLP.
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