The
FDA is negotiating with the drug industry over a possible user fee
increase which, if it goes through, would give the industry even
more in setting the goals and priorities of its supposed regulator.
Industry user fees
were first introduced in the early 1990s in an effort to help speed
up the FDA's approval process; prior to that, the FDA had been
funded entirely by Congress.
But steadily rising
payments have led to drug makers funding more than half of the FDA's
drug review process, giving them immense clout in determining how
the agency is run.
Drug makes
renegotiate the fees with the FDA every five years, meaning they can
have a great deal of input regarding which programs will receive
funding. Regulatory agencies do not normally need to negotiate their
budget with the industries they oversee.
In 1993, $8.9
million of user-fee money accounted for 7 percent of the FDA's drug
review budget. By 2004, the amount had risen to $232 million and 53
percent of the drug review budget.
The Wall Street Journal Online September 1, 2006
Northwest Florida Daily News September 1, 2006
Dr. Mercola's
Comment:
One of the major
reasons why I continually voice my concerns about the
FDA's inability to protect you is their close financial ties to
the drug industry.
Clearly user fees
enacted in the 90s are allowing the drug industry to have
major leverage over the FDA, and that control is continuing
to increase. When the new changes take effect in fiscal 2007, if the
FDA receives all it is seeking, the user fees will account
for two-thirds or more of their drug review budget.
So please realize
that the FDA, as currently configured, cannot adequately protect
your health. What it can, and does, do is further the plans and
profits of the
multi-national drug companies.
Currently,
within the Center for Drug Evaluation and Research, about 80 percent
of the resources are geared towed the approval of drugs and a mere
20 percent is for everything else.
Drug safety is a
measly 5 percent.
Can you possibly
imagine that? Only a nickel out of every dollar is spent on
determining if the drugs are actually safe to use!
This fact
helps reveal their priorities -- priorities that the drug companies
set every five years when the user fees are renegotiated. It is NOT
about protecting you -- it is about approving drugs as quickly as
possible so the drug companies can maximize their profits.
Drugs become
less valuable to the companies when the patent runs out and cheaper,
generic versions can be made. So companies lose $1 million to $2
million EVERY DAY a drug is held up from being marketed to you. So
obviously, the incentive is to get drugs approved as quickly as
possible, even if moving quickly is less safe. And these are
priorities the companies pass on to the agency they fund.
The
fox is guarding the henhouse. And it's going to stay like that
until doctors, patients, and citizens start demanding changes to our
current
fatally flawed system of health care.