Psychiatric Drugs: An Assault on the Human Condition
Street Spirit Interview with Robert Whitaker
Interview by Terry Messman
Bob Whitaker is the author of Mad In America: Bad Science, Bad Medicine, and the Enduring Mistreatment of the Mentally Ill.
Investigative reporter Robert Whitaker, author of the groundbreaking book Mad In America, is
now pursuing a fascinating line of research into how the mammoth
psychiatric drug industry is endangering the American public by
covering up the untold cases of suffering, anguish and disease caused
by the most widely prescribed antidepressants and antipsychotic
medications.
Whitaker exposes the massive lies and
cover-ups that have corrupted the Food and Drug Administration's drug
review process, and co-opted research trials in order to spin the
results of drug tests and conceal the serious hazards and even deadly
side-effects of brand-name drugs like Prozac, Zoloft, Paxil and Zyprexa.
The
story becomes even more frightening when we look at the aggressive
tactics these giant drug companies have used to silence prominent
critics by defaming them in the press, and by using their money and
power to have widely respected scientists and eminent medical
researchers fired for daring to point out the hazards and risks of
suicide and premature death caused by these drugs.
Whitaker
starts by debunking the effectiveness of these massively hyped wonder
drugs -- antidepressants like Prozac, Zoloft and Paxil, and the new
atypical antipsychotic drugs like Zyprexa. His research shows how they
often are barely more effective than placebos in treating mental
disorder and depression, despite the glowing adulation they have
received in the mainstream media.
But he goes on to
make the startling claim that these new psychiatric drugs have directly
contributed to an alarming new epidemic of drug-induced mental illness.
The very drugs prescribed by physicians to stabilize mental disorders
in fact are inducing pathological changes in brain chemistry and
triggering suicide, manic and psychotic episodes, convulsions,
violence, diabetes, pancreatic failure, metabolic diseases, and
premature death.
Whitaker originally was a highly regarded science reporter for the Boston Globe. When he began to research a series on psychiatric issues for the Globe, he was still a believer in the story of progress that psychiatry has been telling the public for decades.
He
said, "I absolutely believed the common wisdom that these antipsychotic
drugs actually had improved things and that they had totally
revolutionized how we treated schizophrenia. People used to be locked
away forever, and now maybe things weren't great, but they were a lot
better. It was a story of progress."
That story of
progress was fraudulent, as Whitaker soon found out when he gained new
insight from his research into torturous psychiatric practices such as
electroshock, lobotomy, insulin coma, and neuroleptic drugs.
Psychiatrists told the public that these techniques "cured" psychosis
or balanced the chemistry of the brain.
But, in
reality, the common thread in all these different treatments was the
attempt to suppress "mental illness" by deliberately damaging the
higher functions of the brain. The stunning truth is that, behind
closed doors, the psychiatric establishment itself labeled these
treatments as "brain-damaging therapeutics."
The
first generation of antipsychotic drugs created a drug-induced brain
pathology by blocking the neurotransmitter dopamine and essentially
shutting down many higher brain functions. In fact, when antipsychotics
such as Thorazine and Haldol were first introduced, psychiatrists
themselves said that these neuroleptic drugs were virtually
indistinguishable from a "chemical lobotomy."
In
recent years, the media have heralded the arrival of so-called designer
drugs like Prozac, Paxil and Zyprexa that are supposed to be superior
and have fewer side effects than the old tricyclic antidepressants and
the first antipsychotics. Millions of Americans have believed this
story and have enriched drug companies like Eli Lilly by spending
billions of dollars annually to purchase these new medications.
Whitaker's
research into the tragic cases of disease, suffering and early deaths
caused by these drugs shows that millions of consumers have been misled
by a massive campaign of lies, distortions, and bought-and-paid-for
drug trials. Eminent medical researchers who have tried to warn us of
the perils of these drugs have been silenced, intimidated and defamed.
In the process, the Food and Drug Administration has become the lapdog
of the giant pharmaceutical industry, not its watchdog.
Street Spirit interviewed
Robert Whitaker about this new "epidemic" of mental disorders, and how
the giant drug companies have profited from selling drugs that make us
sicker.
Street Spirit: Your new
line of research indicates that there has been an enormous rise in the
incidence of mental illness in the United States, despite the seeming
advances in a new generation of psychiatric drugs. Why do you refer to
this increase as an epidemic?
Robert Whitaker: Even
people like the psychiatrist E. Fuller Torrey wrote a book recently in
which he said it looks like we're having an epidemic of mental illness.
When the National Institute of Mental Health publishes its figures on
the incidence of mental illness, you see these rising numbers of
mentally ill people. Some recent reports even say that 20 percent of
Americans now are mentally ill.
So what I wanted to do
was two-fold. I wanted to look into exactly how dramatic is this
increase in mental illness, and particularly severe mental illness.
Part of this rise in the number of people said to be mentally ill is
just definitional. We draw a big wide boundary today and we throw all
sorts of people into that category of mentally ill. So children who are
not sitting neatly enough in their school rooms are said to have
attention deficit hyperactivity disorder (ADHD), and we created a new
disorder called social anxiety disorder.
SS: So
what used to be called simply shyness or anxiety in relating to people
is now labeled a mental disorder and you supposedly need an
antidepressant like Paxil for social anxiety disorder.
RW: Exactly. And you need a stimulant like Ritalin for ADHD.
SS: This
increases psychiatry's clients, but doesn't it also increase the number
of people that giant pharmaceutical companies can sell their
psychiatric drugs to?
RW: Absolutely.
So part of what we're seeing is nothing more than the creation of a
larger market for drugs. If you think about it, as long as we draw as
big a circle as possible, and expand the boundaries of mental illness,
psychiatry can have more clients and sell more drugs. So there's a
built-in economic incentive to define mental illness in as broad terms
as possible, and to find ordinary, distressing emotions or behaviors
that some people may not like and label them as mental illness.
SS: Your
research also shows that there is a real increase in people who have a
severe mental disorder. Now, this seems counterintuitive, but is it
true that you believe much of this increase is caused by the overuse of
some of the new generations of psychiatric drugs?
RW: Yes,
exactly. I looked at the number of the so-called severely disabled
mentally ill -- people who aren't working or who are somehow
dysfunctional because of mental illness. So I wanted to chart through
history the percentage of the population who are considered the
disabled mentally ill.
Now, by 1903, we see that
roughly 1 out of every 500 people in the United States is hospitalized
for mental illness. By 1955, at the start of the modern era of
psychiatric drugs, roughly one out of every 300 people was disabled by
mental illness. Now, let's go to 1987, the end of the first generation
of antipsychotic drugs; and from 1987 forward we get the modern
psychiatric drugs. From 1955 to 1987, during this first era of
psychiatric drugs -- the antipsychotic drugs Thorazine and Haldol and
the tricyclic antidepressants (such as Elavil and Anafranil) -- we saw
the number of disabled mentally ill increase four-fold, to the point
where roughly one out of every 75 persons are deemed disabled mentally
ill.
Now, there was a shift in how we cared for the
disabled mentally ill between 1955 and 1987. In 1955, we were
hospitalizing them. Then, by 1987, we had gone through social change,
and we were now placing people in shelters, nursing homes, and some
sort of community care, and gave them either SSI or SSDI payments for
mental disability. In 1987, we started getting these supposedly better,
second-generation psychiatric drugs like Prozac and the other selective
serotonin re-uptake inhibitor (SSRI) antidepressants. Shortly after
that, we get the new, atypical antipsychotic drugs like Zyprexa
(olanzapine), Clozaril and Risperdal.
What's happened
since 1987? Well, the disability rate has continued to increase until
it's now one in every 50 Americans. Think about that: One in every 50
Americans disabled by mental illness today. And it's still increasing.
The number of mentally disabled people in the United States has been
increasing at the rate of 150,000 people per year since 1987. That's an
increase every day over the last 17 years of 410 people per day newly
disabled by mental illness.
SS: So
that leads to the obvious question. If psychiatry has introduced these
so-called wonder drugs like Prozac and Zoloft and Zyprexa, why is the
incidence of mental illness going up dramatically?
RW: That's
exactly it. This is a scientific question. We have a form of care where
we're using these drugs in an ever more expansive manner, and
supposedly we have better drugs and they're the cornerstone of our
care, so we should see decreasing disability rates. That's what your
expectation would be.
Instead, from 1987 until the
present, we saw an increase in the number of mentally disabled people
from 3.3 million people to 5.7 million people in the United States. In
that time, our spending on psychiatric drugs increased to an amazing
degree. Combined spending on antipsychotic drugs and antidepressants
jumped from around $500 million in 1986 to nearly $20 billion in 2004.
So we raise the question: Is the use of these drugs somehow actually
fueling this increase in the number of the disabled mentally ill?
When
you look at the research literature, you find a clear pattern of
outcomes with all these drugs -- you see it with the antipsychotics,
the antidepressants, the anti-anxiety drugs and the stimulants like
Ritalin used to treat ADHD. All these drugs may curb a target symptom
slightly more effectively than a placebo does for a short period of
time, say six weeks. An antidepressant may ameliorate the symptoms of
depression better than a placebo over the short term.
What
you find with every class of these psychiatric drugs is a worsening of
the target symptom of depression or psychosis or anxiety over the long
term, compared to placebo-treated patients. So even on the target
symptoms, there's greater chronicity and greater severity of symptoms.
And you see a fairly significant percentage of patients where new and
more severe psychiatric symptoms are triggered by the drug itself.
SS: New psychiatric symptoms created by the very drugs people are told will help them recover?
RW:
Absolutely. The most obvious case is with the antidepressants. A
certain percentage of people placed on the SSRIs because they have some
form of depression will suffer either a manic or psychotic attack --
drug-induced. This is well recognized. So now, instead of just dealing
with depression, they're dealing with mania or psychotic symptoms. And
once they have a drug-induced manic episode, what happens? They go to
an emergency room, and at that point they're newly diagnosed. They're
now said to be bipolar and they're given an antipsychotic to go along
with the antidepressant; and, at that point, they're moving down the
path to chronic disability.
SS: Modern
psychiatry claims that these psychiatric drugs correct pathological
brain chemistry. Is there any evidence to back up their claim that
abnormal brain chemistry is the culprit in schizophrenia and depression?
RW: This
is the key thing everyone needs to understand. It really is the answer
that unlocks this mystery of why the drugs would have this long-term
problematic effect. Start with schizophrenia. They hypothesize that
these drugs work by correcting an imbalance of the neurotransmitter
dopamine in the brain.
The theory was that people
with schizophrenia had overactive dopamine systems; and these drugs, by
blocking dopamine in the brain, fixed that chemical imbalance.
Therefore, you get the metaphor that they're like insulin is for
diabetes; they're fixing an abnormality. With the antidepressants, the
theory was that people with depression had too low levels of serotonin;
the drugs upped the levels of serotonin in the brain and therefore
they're balancing the brain chemistry.
First of all,
those theories never arose from investigations into what was actually
happening to people. Rather, they would find out that antipsychotics
blocked dopamine and so they theorized that people had overactive
dopamine systems. Same with the antidepressants. They found that
antidepressants upped the levels of serotonin; therefore, they
theorized that people with depression must have low levels of serotonin.
But
here is the thing that one wishes all of America would know and wishes
psychiatry would come clean on: They've never been able to find that
people with schizophrenia have overactive dopamine systems. They've
never been able to find that people with depression have underactive
serotonin systems. They've never found consistently that any of these
disorders are associated with any chemical imbalance in the brain. The
story that people with mental disorders have known chemical imbalances
-- that's a lie. We don't know that at all. It's just something that
they say to help sell the drugs and help sell the biological model of
mental disorders.
But the kicker is this. We do know,
in fact, that these drugs perturb how these chemical messengers work in
the brain. The real paradigm is: People diagnosed with mental disorders
have no known problem with their neurotransmitter systems; and these
drugs perturb the normal function of neurotransmitters.
SS: So rather than fixing a chemical imbalance, these widely prescribed drugs distort the brain chemistry and make it pathological.
RW:
Absolutely. Stephen Hyman, a well-known neuroscientist and the former
director of the National Institute of Mental Health, wrote a paper in
1996 that looked at how psychiatric drugs affect the brain. He wrote
that all these drugs create perturbations in neurotransmitter
functions. And he notes that the brain, in response to this drug from
the outside, alters its normal functions and goes through a series of
compensatory adaptations.
In other words, it tries to
adapt to the fact that an antipsychotic drug is blocking normal
dopamine functions. Or in the case of antidepressants, it tries to
compensate for the fact that you're blocking a normal reuptake of
serotonin. The way it does this is to adapt in the opposite way. So, if
you're blocking dopamine in the brain, the brain tries to put out more
dopamine and it actually increases the number of dopamine receptors. So
a person placed on antipsychotic drugs will end up with an abnormally
high number of dopamine receptors in the brain.
If you
give someone an antidepressant, and that tries to keep serotonin levels
too high in the brain, it does exactly the opposite. It stops producing
as much serotonin as it normally does and it reduces the number of
serotonin receptors in the brain. So someone who is on an
antidepressant, after a time ends up with an abnormally low level of
serotonin receptors in the brain. And here's what Hyman concluded about
this: After these changes happened, the patient's brain is functioning
in a way that is "qualitatively as well as quantitatively different
from the normal state." So what Stephen Hyman, former head of the NIMH,
has done is present a paradigm for how these drugs affect the brain
that shows that they're inducing a pathological state.
SS: So
the paradox is there's no evidence for modern psychiatry's claim that
there is any pathological biochemical imbalance in the brain that
causes mental illness, but if you treat people with these new wonder
drugs, that is what creates a pathological imbalance?
RW: Yes,
these drugs disrupt normal brain chemistry. That's the real paradox
here. And the real tragedy is, that even as we peddle these drugs as
chemical balancers, chemical fixers, in truth we're doing precisely the
opposite. We're taking a brain that has no known abnormal brain
chemistry, and by placing people on the drugs, we're perturbing that
normal chemistry. Here's how Barry Jacobs, a Princeton neuroscientist,
describes what happens to a person given an SSRI antidepressant. "These
drugs," he said, "alter the level of synaptic transmission beyond the
physiologic range achieved under normal environmental biological
conditions. Thus, any behavioral or physiologic change produced under
these conditions might more appropriately be considered pathologic
rather than reflective of the normal biological role of serotonin."
SS: One
of the SSRI antidepressants that's widely believed to be a wonder drug
is Prozac. Yet your research found that the Food and Drug
Administration (FDA) received more adverse reports about Prozac than
any other drug. What sort of ill effects were people reporting?
RW:
First of all, with Prozac and the SSRIs that followed, their level of
efficacy was always of a very minor sort. In all the clinical trials of
the antidepressants, roughly 41 percent of the patients got better in
the short term versus 31 percent of the patients on placebo. Now just
one other caveat on that. If you use an active placebo in these trials
-- an active placebo causes a physiologic change with no benefit, like
a dry mouth -- any difference in outcome between the antidepressant and
placebo virtually disappears.
SS: Weren't the early drug tests of Prozac so unpromising that they had to manipulate test results to get FDA approval at all?
RW:
What happened with Prozac is a fascinating story. Right from the
beginning, they noticed only very marginal efficacy over placebo; and
they noticed that they had some problems with suicide. There were
increased suicidal responses compared to placebo. In other words, the
drugs was agitating people and making people suicidal who hadn't been
suicidal before. They were getting manic responses in people who hadn't
been manic before. They were getting psychotic episodes in people who
hadn't been psychotic before. So you were seeing these very problematic
side effects even at the same time that you were seeing very modest
efficacy, if any, over placebo in ameliorating depression.
Basically,
what Eli Lilly (Prozac's manufacturer) had to do was cover up the
psychosis, cover up the mania; and, in that manner, it was able to get
these drugs approved. One FDA reviewer even warned that Prozac appeared
to be a dangerous drug, but it was approved anyway.
We're
seemingly finding all this out only now: "Oh, Prozac can cause suicidal
impulses and all these SSRIs may increase the risk of suicide." The
point is, that wasn't anything new. That data was there from the very
first trial. You had people in Germany saying, "I think this is a
dangerous drug."
SS: Even back in the late 1980s, they already knew?
RW: Before
the late 1980s -- in the early '80s, before Prozac gets approved.
Basically what Eli Lilly had to do was cover up that risk of mania and
psychosis, cover up that some people were becoming suicidal because
they were getting this nervous agitation from Prozac. That's the only
way it got approved.
There were various ways they did
the cover-up. One was just to simply remove reports of psychosis from
some of the data. They also went back and recoded some of the trial
results. Let's say someone had a manic episode or a psychotic episode;
instead of putting that down, they would just put down a return of
depression, and that sort of thing. So there was a basic need to hide
these risks right from the beginning, and that's what was done.
So
Prozac gets approved in 1987, and it's launched in this amazing PR
campaign. The pill itself is featured on the cover of several
magazines! It's like the Pill of the Year [laughs]. And it's said to be
so much safer: a wonder drug. We have doctors saying, "Oh, the real
problem with this drug is that we can now create whatever personality
we want. We're just so skilled with these drugs that if you want to be
happy all the time, take your pill!"
That was
complete nonsense. The drugs were barely better than placebo at
alleviating depressive symptoms over the short term. You had all these
problems; yet we were touting these drugs, saying, "Oh, the powers of
psychiatry are such that we can give you the mind you want -- a
designer personality!" It was absolutely obscene. Meanwhile, which
drug, after being launched, quickly became the most complained about
drug in America? Prozac!
SS: What were the level of complaints when Prozac hit the market?
RW:
In this county, we have Medwatch, a reporting system in which we report
adverse events about psychiatric drugs to the FDA. By the way, the FDA
tries to keep these adverse reports from the public. So, instead of the
FDA making these easily available to the public. so you can know about
the dangers of the drugs, it's very hard to get these reports.
Within
one decade, there were 39,000 adverse reports about Prozac that were
sent to Medwatch. The number of adverse events sent to Medwatch is
thought to represent only one percent of the actual number of such
events. So, if we get 39,000 adverse event reports about Prozac, the
number of people who have actually suffered such problems is estimated
to be 100 times as many, or roughly four million people. This makes
Prozac the most complained about drug in America, by far. There were
more adverse event reports received about Prozac in its first two years
on the market than had been reported on the leading tricyclic
antidepressant in 20 years.
Remember, Prozac is
pitched to the American public as this wonderfully safe drug, and yet
what are people complaining about? Mania, psychotic depression,
nervousness, anxiety, agitation, hostility, hallucinations, memory
loss, tremors, impotence, convulsions, insomnia, nausea, suicidal
impulses. It's a wide range of serious symptoms.
And
here's the kicker. It wasn't just Prozac. Once we got the other SSRIs
on the market, like Zoloft and Paxil, by 1994, four SSRI
antidepressants were among the top 20 most complained about drugs on
the FDA's Medwatch list. In other words, every one of these drugs
brought to market started triggering this range of adverse events. And
these were not minor things. When you talk about mania, hallucinations,
psychotic depression, these are serious adverse events.
Prozac
was pitched to the American public as a wonder drug. It was featured on
the covers of magazines as so safe, and as a sign of our wonderful
ability to effect the brain just as we want it. In truth, the reports
were showing it could trigger a lot of dangerous events, including
suicide and psychosis.
The FDA was being warned about
this. They were getting a flood of adverse event reports, and the
public was never told about this for the longest period of time. It
took a decade for the FDA to begin to acknowledge the increased
suicides and the violence it can trigger in some people. It just shows
how the FDA betrayed the American people. This is a classic example.
They betrayed their responsibility to act as a watchdog for the
American people. Instead they acted as an agency that covered up harm
and risk with these drugs.
SS: In
light of the FDA's failure to warn us about Prozac, what about their
recent negligence on the issue of the risk of suicide in children given
antidepressants like Paxil? Weren't England's mental health officials
far better than their American counterparts in the FDA in warning about
the dangers of suicidal attempts when antidepressants are given to
youth?
RW: Yes. The children's
story is unbelievably tragic. It's also a really sordid story. Let's go
back a little to see what happened to children and antidepressants.
Prozac comes to market in 1987. By the early 1990s, the pharmaceutical
companies making these drugs are saying, "How do we expand the market
for antidepressants?" Because that's what drug companies do -- they
want to get to an ever-larger number of people. They saw they had an
untapped market in kids. So let's start peddling the drugs to kids. And
they were successful. Since 1990, the use of antidepressants in kids
went up something like seven-fold. They began prescribing them
willy-nilly.
Now, whenever they did pediatric trials of
antidepressants, they found that the drugs were no more effective on
the target symptom of depression than placebo. This happened again and
again in the pediatric drug trials of antidepressants. So, what that
tells you is there is no real therapeutic rationale for the drugs
because in this population of kids, the drugs don't even curb the
target symptoms over the short term any better than placebo; and yet
they were causing all sorts of adverse events.
For
example, in one trial, 75 percent of youth treated with antidepressants
suffered an adverse event of some kind. In one study by the University
of Pittsburgh, 23 percent of children treated with an SSRI developed
mania or manic-like symptoms; an additional 19 percent developed
drug-induced hostility. The clinical results were telling you that you
didn't get any benefit on depression; and you could cause all sorts of
real problems in kids -- mania, hostility, psychosis, and you may even
stir suicide. In other words, don't use these drugs, right? It was
absolutely covered up.
SS: How was it covered up?
RW: We
had psychiatrists -- some of those obviously getting money from the
drug companies -- saying the kids are under-treated and they're at risk
of suicide and how could we possibly treat kids without these pills and
what a tragedy it would be if we couldn't use these antidepressants.
Finally,
a prominent researcher in England, David Healy, started doing his own
research on the ability of these drugs to stir suicide. He also managed
to get access to some of the trial results and he blew the whistle. He
first blew the whistle in England and he presented this data to the
review authorities there. And they saw that it looks like these drugs
are increasing the risk of suicide and there are really no signs of
benefits on the target symptoms of depression. So they began to move
there to warn doctors not to prescribe these drugs to youth.
What
happens in the United States? Well, it's only after there's a lot of
pressure put on the FDA that they even hold a hearing. The FDA sort of
downplays the risk of these drugs. They're slow to even put black box
warnings on them. Why? Aren't kids lives worth protecting? If we know
that we have a scientifically shown risk that these drugs increase
suicide, shouldn't you at least warn about it? But the FDA was even
digging in its heels about putting that black box warning on the drugs.
SS: If
Prozac is the nation's most complained about drug, if Paxil is shown to
be a suicide risk for youth, how do these antidepressants continue to
have a reputation as near-magic cures for depression? And why did the
FDA failed to warn us about Paxil and Prozac for such a long time?
RW: There's
a couple reasons for that. The FDA's funding changed in the 1990s. An
act was passed in which a lot of the FDA's funding came from the drug
industry: the PDUFA Act, or Prescription Drug User Fee Act. Basically,
when drug companies applied for FDA approval they had to pay a fee.
Those fees became what is funding a large portion of the FDA's review
of drug applications.
So all of a sudden, the funding
is coming from the drug industry; it's no longer coming from the
people. As that act comes up for renewal, basically the drug lobbyists
are telling the FDA that their job is no longer to be critically
analyzing drugs, but to approve drugs quickly. And that was part of
Newt Gingrich's thing: Your job is to get these drugs to market. Start
partnering with the drug industry and facilitating drug development. We
lost this idea that the FDA had a watchdog role.
Also,
in a human way, a lot of people who work for the FDA leave there and
end up going to work for the drug companies. The old joke is that the
FDA is sort of like a showcase for a future job in the drug industry.
You go there, you work awhile, then you go off into the drug industry.
Well, if that's the progression that people make, in essence they're
making good old boy network connections, so they're not going to be so
harsh on the drug companies. So, that's what really happened in the
1990s. The FDA was given new marching orders. The orders were:
"Facilitate getting drugs to market. Don't be too critical. And, in
fact, if you want to keep your funding, which was coming now from the
drug industry, make sure you take these lessons to heart."
SS: So
the giant pharmaceutical companies have a vast amount of power to cook
the results of drug tests and make researchers and even the FDA itself
bow to their will?
RW: The FDA, in
essence, was kneecapped in the early 1990s, and we really saw it with
the psychiatric drugs. The FDA became a lapdog for the pharmaceutical
industry, not a watchdog.
It's only now that this has become common knowledge. We have Marcia Angell, the former editor of the New England Journal of Medicine, write
a book in which she says that the FDA became a lapdog. It's basically
now well recognized that you had this decline and fall. As the editor
of the New England Journal of Medicine, the most prestigious
medical journal we have, Marcia Angell is someone who was at the very
heart of American medicine, and she concluded that the FDA let down the
American people. And she lost her job at the New England Journal of Medicine for starting to criticize pharmaceutical companies.
She
was the editor of the journal in the late 1990s and there was a
corresponding doctor named Thomas Bodenheimer who decided to write an
article about how you couldn't even trust what was published in the
medical journals anymore because of all the spinning of results.
So they did an investigation about how the pharmaceutical companies are
funding all the research and spinning the trial results, so you can no
longer really trust what you read in scientific journals. They pointed
out that when they tried to get an expert to review the scientific
literature related to antidepressants, they basically couldn't find
someone who hadn't taken money from the drug companies.
Now, the New England Journal of Medicine is
published by the Massachusetts Medical Society which publishes a lot of
other journals, and they get a lot of pharmaceutical advertising. So
what happens after that article appears by Thomas Bodenheimer and an
accompanying editorial by Marcia Angell about the sorry state of
American medicine because of this? They both lose their jobs! She's
gone and so is Thomas Bodenheimer. Think about this. We have the
leading medical journal firing people, letting them go, because they
dared to criticize the dishonest science and the dishonest process that
was poisoning the scientific literature.
So we have the
FDA that's acting as lapdogs. You can't trust the scientific
literature. All this shows how the American public was betrayed and
didn't know about all the problems with these drugs and why it was kept
from them. It has to do with money, prestige and old boy networks.
SS: It
also has to do with the silencing of critics. Eli Lilly uses the media
to trumpet Prozac's benefits and gives perks to doctors to attend
conferences to hear about its benefits, and buys off researchers. But
don't they also use their power and money to silence their critics?
RW: An
example is Dr. Joseph Glenmullen, a psychiatrist who also works for
Harvard University Health Services, and who wrote a book called Prozac
Backlash to warn about the dangers of Prozac. He's finding that the
drugs are being overused and cause severe side effects. He even raises
questions about long-term memory problems with the drugs and cognitive
dysfunction. Well, Eli Lilly then mounted a public relations campaign
to try to discredit him. They sent out notices to the media questioning
his affiliation with Harvard Medical School, etc. It was all about
silencing the critics.
If you sing the tune that the
drug companies want, at the very top levels, you get paid a lot of
money to fly around and give presentations about the wonders of the
drugs. And those who come, and don't ask any embarrassing questions,
get the lobster dinners and maybe they get a little honorarium for
attending this educational meeting. So if you want to be part of this
gravy train, you can. You sing the wonders of the drug, and you don't
talk about their nasty side effects, and you can get a nice payment as
one of their guest speakers, as one of their experts.
But
if you're one of the ones saying, "What about the mania, what about the
psychosis?" -- they do silence you. Look at what happened to David
Healy. Healy is even the best example. David Healy has this sterling
reputation in England. He's written several books on the history of
psychopharmacology. He's like the former Secretary of the
Psychopharmacology Association over there. He gets offered a job at the
University of Toronto to head up their psychiatry department. So while
he's waiting to assume that position at the University of Toronto, he
goes to Toronto and delivers a talk on the elevated risk of suicide
with Prozac and some of the other SSRIs. By the time he's back home,
the job offer has been rescinded.
Now does Eli Lilly
donate some money to the University of Toronto? Absolutely. So, to
answer your question, yes, Eli Lilly silences dissenters as well.
SS: What
is the story behind the secret settlement between Eli Lilly and the
survivors who sued the company after Joseph Wesbecker shot 20 coworkers
after being put on Prozac?
RW: During
this trial in which Eli Lilly was being sued, the judge was going to
allow some very damaging evidence showing wrongdoing by Eli Lilly in a
previous instance. The judge said, "Go ahead and introduce this at the
trial." But next thing you know, they don't introduce this; and in
fact, all of a sudden, the plaintiffs no longer are presenting very
damaging evidence to make their case. So the judge wonders why they are
not presenting their best case anymore. He smells a rat. He suspects
Eli Lilly has settled with the plaintiffs secretly and the deal is
that, as part of this settlement, the plaintiffs will go ahead with a
sham trial so that Eli Lilly will win the trial. Then Eli Lilly can
claim, "See our drug doesn't cause people to become violent."
And,
indeed, that's what happened. Eli Lilly felt it was going to lose this
trial. They went to the plaintiffs and said they would give them a lot
of money. They agreed to go ahead and settle the case, but had the
plaintiffs go ahead with the trial. That way Eli Lilly can publicly
claim that they won the trial and Prozac doesn't cause harm.
SS: How did this even come out into the light of day?
RW: We
would never have known about this except for two things. One, believe
it or not, the judge, in essence, appealed the decision in his own
court. He said, "I smell a rat." And through that, he found out that
there was this secret settlement and that it was a sham proceeding that
continued on. He said it was one of the worst violations of the
integrity of the legal process that he'd ever seen. And second, an
English journalist named John Cornwell wrote a book called Power to Harm: Mind, Medicine, and Murder on Trial.
He wrote about this case, and yet in the United States, we got almost
no news about this secret settlement and this whole perversion of the
legal process. It was an English journalist who was exposing this story.
My
point here is this: They silence people like Marcia Angell. They
pervert the scientific process. They pervert the legal process. They
pervert the FDA drug review process. It's everywhere! And that's how we
as a society end up believing in these psychiatric drugs. You asked the
question a while back, "Why do we still believe in Prozac?" One of the
reasons is that the story about Prozac is, in effect, maintained. It's
publicly maintained because we do all this silencing along all these
lines.
The other thing to remember is that some people
on Prozac do feel better. That's true. That shows up, just in the same
way that some people on placebos feel better. And those are the stories
that get repeated: "Oh, I took Prozac and I'm feeling better." It's
that select group that does better that becomes the story that is told
out there, and the story that the public hears. So that's why we
continued to believe in the story of these wonder drugs that are very
safe in spite of all this messy stuff that gets covered up.
SS: Let's
now move from the antidepressants like Prozac to consider another new
group of supposed wonder drugs -- the new antipsychotic drugs. You
write that long-term use of antipsychotic drugs -- both the original
neuroleptic drugs like Thorazine and Haldol and the newer atypicals
like Zyprexa and Risperdal -- cause pathological changes in the brain
that can lead to a worsening of the symptoms of mental illness. What
changes in brain chemistry result from the antipsychotics, and how can
that lead to the most frightening prospect you describe -- chronic
mental illness that is locked in by these drugs?
RW: This
is a line of research that goes across 40 years. This problem of
chronic illness shows up time and time again in the research
literature. This biological mechanism is somewhat well understood now.
The antipsychotics profoundly block dopamine receptors. They block
70-90 percent of the dopamine receptors in the brain. In return, the
brain sprouts about 50 percent extra dopamine receptors. It tries to
become extra sensitive.
So in essence you've created an
imbalance in the dopamine system in the brain. It's almost like, on one
hand, you've got the accelerator down -- that's the extra dopamine
receptors. And the drug is the brake trying to block this. But if you
release that brake, if you abruptly go off the drugs, you now do have a
dopamine system that's overactive. You have too many dopamine
receptors. And what happens? People that go abruptly off of the drug,
do tend to have severe relapses.
SS: So
people that have been treated with these antipsychotic drugs have a far
greater tendency to relapse, and have new episodes of mental illness,
as opposed to people who have had other kinds of non-drug therapies?
RW: Absolutely,
and that was understood by 1979, that you were actually increasing the
underlying biological vulnerability to the psychosis. And by the way,
we sort of understood that if you muck with the dopamine system, that
you could cause some symptoms of psychosis with amphetamines. So if you
give someone amphetamines enough, they're at increased risk of
psychosis. This is well known. And what do amphetamines do? They
release dopamine. So there is a biological reason why, if you're
mucking up the dopamine system, you're increasing the risk of
psychosis. That's in essence what these antipsychotic drugs do, they
muck up the dopamine system.
Here's just one real
powerful study on this: Researchers with the University of Pittsburgh
in the 1990s took people newly diagnosed with schizophrenia, and they
started taking MRI pictures of the brains of these people. So we get a
picture of their brains at the moment of diagnosis, and then we prepare
pictures over the next 18 months to see how those brains change. Now
during this 18 months, they are being prescribed antipsychotic
medications, and what did the researchers report? They reported that,
over this 18-month period, the drugs caused an enlargement of the basal
ganglia, an area of the brain that uses dopamine. In other words, it
creates a visible change in morphology, a change in the size of an area
of the brain, and that's abnormal. That's number one. So we have an
antipsychotic drug causing an abnormality in the brain.
Now
here's the kicker. They found that as that enlargement occurred, it was
associated with a worsening of the psychotic symptoms, a worsening of
negative symptoms. So here you actually have, with modern technology, a
very powerful study. By imaging the brain, we see how an outside agent
comes in, disrupts normal chemistry, causes an abnormal enlargement of
the basal ganglia, and that enlargement causes a worsening of the very
symptoms it's supposed to treat. Now that's actually, in essence, a
story of a disease process -- an outside agent causes abnormality,
causes symptoms...
SS: But in this
case, the outside agent that triggers the disease process is the
supposed cure for the disease! The psychiatric drug is the
disease-causing agent.
RW: That's
exactly right. It's a stunning, damning finding. It's the sort of
finding you would say, "Oh Christ, we should be doing something
different." Do you know what those researchers got new grants for,
after they reported that?
SS: No, what? You'd guess they got funding to carry out these same studies on other classes of psychiatric drugs.
RW: They
got a grant to develop an implant, a brain implant, that would deliver
drugs like Haldol on a continual basis! A grant to develop a drug
delivery implant so you could implant this in the brains of people with
schizophrenia and then they wouldn't even have a chance not to take the
drugs!
SS: Unbelievable. Designing
an implant to provide a constant dose of a drug that they had just
discovered causes pathology in the brain chemistry.
RW: Right,
they had just found that they're causing a worsening of symptoms! So
why would you go on to a design a permanent implant? Because that's
where the money was.
And no one wanted to deal with this horrible
finding of an enlargement of the basal ganglia caused by the drugs, and
that is associated with the worsening of symptoms. No one wanted to
deal with the fact that when you look at people medicated on
antipsychotics, you start to see a shrinking of the frontal lobes. No
one wants to talk about that either. They stopped that research.
SS: What other side effects are caused by prolonged use of these antipsychotic drugs?
RW:
Oh, you get tardive dyskinesia, a permanent brain dysfunction; and
akathisia, which is this incredible nervous agitation. You're just
never comfortable. You want to sit but you can't sit. It's like you're
crawling out of your own skin. And it's associated with violence,
suicide and all sorts of horrible things.
SS: Those
kinds of side-effects were notorious with the first generation of
antipsychotic drugs, like Thorazine, Haldol and Stelazine. But, just as
with Prozac, so many people are still touting the new generation of
atypical antipsychotics -- Zyprexa, Clozaril and Risperdal -- as wonder
drugs that control mental illness with far fewer side effects. Is that
true? What have you found?
RW: No,
it's just complete nonsense. In fact, I think the newer drugs will
eventually be seen as more dangerous than the old drugs, if that's
possible. As you know, the standard neuroleptics like Thorazine and
Haldol have had quite a litany of harm with the tardive dyskinesia and
all.
So when we got the new atypical drugs, they were touted as
so much safer. But with these new atypicals, you get all sorts of
metabolic dysfunctions.
Let's
talk about Zyprexa. It has a different profile. So it may not cause as
much tardive dyskinesia. It may not cause as many Parkinsonian
symptoms. But it causes a whole range of new symptoms. So, for example,
it's more likely to cause diabetes. It's more likely to cause
pancreatic disorders. It's more likely to cause obesity and
appetite-disregulation disorders.
In fact,
researchers in Ireland reported in 2003 that since the introduction of
the atypical antipsychotics, the death rate among people with
schizophrenia has doubled. They have done death rates of people treated
with standard neuroleptics and then they compare that with death rates
of people treated with atypical antipsychotics, and it doubles. It
doubles! It didn't reduce harm. In fact, in their seven-year study, 25
of the 72 patients died.
SS: What were the causes of death?
RW: All
sorts of physical illnesses, and that's part of the point. You're
getting respiratory problems, you're getting people dying of incredibly
high cholesterol counts, heart problems, diabetes. With olanzapine
(Zyprexa), one of the problems is that you're really screwing up the
core metabolic system. That's why you get these huge weight gains, and
you get the diabetes. Zyprexa basically disrupts the machine that we
are that processes food and extracts energy from that food. So this
very fundamental thing that we humans do is disrupted, and at some
point you just see all these pancreatic problems, faulty glucose
regulation, diabetes, etc. That's really a sign that you're mucking
with something very fundamental to life.
SS: There's
supposedly an alarming increase in mental illness being diagnosed in
children. Millions are diagnosed with depression, bipolar and psychotic
symptoms, attention deficit hyperactivity disorder, and social anxiety
disorder. Is this explosive new prevalence of mental illness among
children a real increase, or is it a marketing campaign that enriches
the psychiatric drug industry, a bonanza for the pharmaceutical
corporations?
RW: You're touching
on something now that is a tragic scandal of monumental proportions. I
talk sometimes to college classes, psychology classes. You cannot
believe the percentage of youth who have been told they were mentally
ill as kids, that something was wrong with them. It's absolutely
phenomenal. It's absolutely cruel to be telling kids that they have
these broken brains and mental illnesses.
There's two
things that are happening here. One, of course, is that it's complete
nonsense. As you remember as a kid, you have too much energy or you
behave sometimes in not altogether appropriate ways, and you do have
these extremes of emotions, especially during your teenage years. Both
children and teenagers can be very emotional. So one thing that's going
on is that they take childhood behaviors and start defining behaviors
they don't like as pathological. They start defining emotions that are
uncomfortable as pathological. So part of what we're doing is
pathologizing childhood with straight-out definition stuff. We're
pathologizing poverty among kids.
For example, if
you're a foster kid, and maybe you drew a bad straw in the lottery of
life and are born into a dysfunctional family and you get put into
foster care, do you know what happens today? You pretty likely are
going to get diagnosed with a mental disorder, and you're going to be
placed on a psychiatric drug. In Massachusetts, it's something like 60
to 70 percent of kids in foster care are now on psychiatric drugs.
These kids aren't mentally ill! They got a raw deal in life. They ended
up in a foster home, which means they were in a bad family situation,
and what does our society do? They say: "You have a defective brain."
It's not that society was bad and you didn't get a fair deal. No, the
kid has a defective brain and has to be put on this drug. It's
absolutely criminal.
Let's talk about bipolar disorder
among kids. As one doctor said, that used to be so rare as to be almost
nonexistent. Now we're seeing it all over. Bipolar is exploding among
kids. Well, partly you could say that we're just slapping that label on
kids more often; but in fact, there is something real going on. Here's
what's happening. You take kids and put them on an antidepressant --
which we never used to do -- or you put them on a stimulant like
Ritalin. Stimulants can cause mania; stimulants can cause psychosis.
SS: And antidepressants can also cause mania, as you pointed out.
RW:
Exactly, so the kid ends up with a drug-induced manic or psychotic
episode. Once they have that, the doctor at the emergency room doesn't
say, "Oh, he's suffering from a drug-induced episode." He says he's
bipolar.
SS: Then they give him a whole new drug for the mental disorder caused by the first drug.
RW: Yeah,
they give him an antipsychotic drug; and now he's on a cocktail of
drugs, and he's on a path to becoming disabled for life. That's an
example of how we're absolutely making kids sick.
SS: It's
like society or their schools are trying to make them manageable and
they end up putting them on a chemical roller coaster against their
will.
RW: Absolutely.
SS: There's
an astonishing number of kids being given Ritalin to cure
hyperactivity. But what 10-year-old boy in a confined school setting
isn't hyperactive? You write that the effect of Ritalin on the dopamine
system is very similar to cocaine and amphetamines.
RW: Ritalin
is methylphenidate. Now methylphenidate affects the brain in exactly
the same way as cocaine. They both block a molecule that is involved in
the reuptake of dopamine.
SS: So they both increase the dopamine levels in the brain?
RW: Exactly.
And they do it with a similar degree of potency. So methylphenidate is
very similar to cocaine. Now, one difference is whether you're snorting
it or if it's in a pill. That partly changes how quickly it's
metabolized. But still, it basically affects the brain in the same way.
Now, methylphenidate was used in research studies to deliberately stir
psychosis in schizophrenics. Because they knew that you could take a
person with a tendency towards psychosis, give them methylphenidate,
and cause psychosis. We also knew that amphetamines, like
methylphenidate, could cause psychosis in people who had never been
psychotic before.
So think about this. We're giving a
drug to kids that is known to have the possibility of stirring
psychosis. Now, the odd thing about methylphenidate and amphetamines is
that, in kids, they sort of have a counterintuitive effect. What does
speed do in adults? It makes them more jittery and hyperactive. For
whatever reasons, in kids amphetamines will actually still their
movements; it will actually keep them in their chairs and make them
more focused. So you've got kids in boring schools. The boys are not
paying attention and they're diagnosed with ADHD and put on a drug that
is known to stir psychosis. The next thing you know, a fair number of
them are not doing well by the time they're 15, 16, 17. Some of those
kids talk about how when you're on these drugs for the long term, you
start feeling like a zombie; you don't feel like yourself.
SS: Hollowed-out, blunted emotions. And this is being done to millions of kids.
RW:
Millions of kids! Think about what we're doing. We're robbing kids of
their right to be kids, their right to grow, their right to experience
their full range of emotions, and their right to experience the world
in its full hue of colors. That's what growing up is, that's what being
alive is! And we're robbing kids of their right to be. It's so
criminal. And we're talking about millions of kids who have been
affected this way. There are some colleges where something like 40 to
50 percent of the kids arrive with a psychiatric prescription.
SS: It
looks like a huge social-control mechanism. Society gives kids Ritalin
and antidepressants to subdue them and make them conform. On the one
hand, it's all about social control and conformity. But it also has a
huge marketing payoff.
RW: You're
right, it creates customers for the drugs, and hopefully lifelong
customers. That's what they're told, aren't they? They're told they are
going to be on these drugs for life. And next thing they know, they're
on two or three or four drugs. It's brilliant from the capitalist point
of view. It does serve some social-control function. But you take a
kid, and you turn them into a customer, and hopefully a lifelong
customer. It's brilliant.
We now spend more on
antidepressants in this country than the Gross National Product of
mid-sized countries like Jordan. It's just amazing amounts of money.
The amount of money we spend on psychiatric drugs in this country is
more than the Gross National Product of two-thirds of the world's
countries. It's just this incredibly lucrative paradigm of the mind
that you can fix chemical imbalances in the brain with these drugs. It
works so well from a capitalistic point of view for Eli Lilly. When
Prozac came to market, Eli Lilly's value on Wall Street, its
capitalization, was around 2 billion dollars. By the year 2000, the
time when Prozac was its number-one drug, its capitalization reached 80
billion dollars -- a forty-fold increase.
So that's
what you really have to look at if you want to see why drug companies
have pursued this vision with such determination. It brings billions of
dollars in wealth in terms of increased stock prices to the owners and
managers of those companies. It also benefits the psychiatric
establishment that gets behind the drugs; they do well by this. There's
a lot of money flowing in the direction of those that will embrace this
form of care. There's advertisements that enrich the media. It's all a
big gravy train.
Unfortunately, the cost is dishonesty
in our scientific literature, the corruption of the FDA, and the
absolute harm done to children in this country drawn into this system,
and an increase of 150,000 newly disabled people every year in the
United States for the last 17 years. That's an incredible record of
harm done.
SS: Everyone gets
rich -- the drug companies, the psychiatrists, the researchers, the
advertising agencies -- and the clients get drugged out of their minds
and damaged for life.
RW: And you
know what's interesting? No one says that the mental health of the
American people is getting better. Instead, everyone says we have this
increasing problem They blame it on the stresses of modern life or
something like that, and they don't want to look at the fact that we're
creating mental illness.
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