Toxic Psychiatric Drugs
 
http://www.canadiandimension.mb.ca/v35/v35_5ab.htm#three 
Prescription For Scandal: Biological Psychiatry's 
Faustian Pact Canadian Dimension September/October 2001
By Athony Black The last few decades have
witnessed an explosion in the use of psychiatric
medication. Indeed, the omnipresence of legal brain
altering drugs in our society is such that, nowadays, it is rare for us not to know someone else
who is on them - if we not already taking them ourselves. Moreover, and contrary to popular
perception, a marked increase in the practice of electro-shock therapy is
accompanying this legal drug explosion. Prior to 1960 this biological
psychiatric arsenal was confined mostly within the walls of the
major psychiatric institutions. Since then, the biological genie has escaped the confines of
the mental institution and taken up residence amidst the population at large. One of the reasons for
this psychiatric colonization of the normal, stems from the increasingly intimate association
between the multi-billion dollar a year psycho-pharmaceutical industry and
institutional psychiatry. Thus, the latter's psychiatric journals,
conventions and professional associations are all substantially underwritten by the
former. Another reason is the rapid growth in Western society of an overarching philosophy of what
is known as biological reductionism. This notion posits that, in studying any higher
organizational entity, the whole can be explained by the parts, the
complex by the simple, the higher by the lower. If you are 'depressed',
it is because you have a biochemical imbalance, rather than,
perhaps, that your life has no meaning. If one goes to war it is because of
individual 'aggressive genes', rather than your being the pawn of complex
socio-political forces over which you have no control. A third and perhaps more
ominous reason for the dramatic rise in the fortunes
of biological psychiatry, is that its proponents have waged a propaganda war on its behalf
that is riven with pseudo-scientific claims and evidential suppression. Shock/Drug Therapy and
Brain Damage They continue to claim, for instance, against substantial
research to the contrary, that shock therapy is harmless. Needless to say, no
psychiatrists have ever volunteered to test this hypothesis
themselves. In this they are probably wise, since the original animal
research (of the 1940' and 50's) demonstrating undeniable brain damage was damning
in this regard, as has been much of the subsequent human clinical data. Particularly
disturbing are the demographic trends for this controversial procedure.
In Canada and the United States, well over 100,000 people are
subjected to the electroshock every year. Over two thirds of these
patients are women, and almost half are the elderly. Still, while ECT is one of the 
heavy weapons of the modern bio-psych arsenal, the more
usual work-a-day armament is drug therapy. The first is targeted
on a population of thousands. The second on millions. Here again, proponents make a
number of bold claims. Perhaps the most scandalous of
these is that drug therapy is safe. In 1980, twenty-five years after the introduction of
neuroleptic (antipsychotic) medication, an American Psychiatric Association
task force report finally, grudgingly confirmed what a number of previously
neglected studies had attempted to call attention to, namely, that
roughly 40 percent of chronic users of these drugs went on to develop tardive dyskinesia,
a Parkinsonian-like movement disorder indicative of permanent brain damage. Subsequent
studies only amplified these fears by pointing the finger at other
permanent brain disorders caused by the neuroleptics. These included tardive akithisia,
a highly debilitating anxiety and hyperactive movement disorder. All told, the evidence
now in supports rates of neuroleptic induced brain damage exceeding
an astounding 5 percent per year of usage. For clearly psychotic patients
there may be a cost-benefit tradeoff to consider. except that few if any
of the patients so prescribed are, or ever have been, told of the
potential cost. Moreover, these drugs are routinely employed in
institutional settings on clients that are patently not psychotic. Given this sobering tale,
it might have been expected that biological psychiatry would exercise the cautionary
principle in its future endeavours. This was not the case.
Instead, the next round in psychiatry's legal drug trafficking campaign
was launched on an unsuspecting public with all the same hubris, euphoria
and woefully inadequate, experimental investigation as the first. So Began the Anti-depressant
Revolution. Actually, the word 'revolution' is slightly misleading here, for
some of the anti-depressants, like the tricyclics and the monoamine oxidase inhibitors,
have been around for quite a while. Long enough, in fact, to garner a
shadowy reputation. Thus, the tricyclics, like Tofranil and Elavil, are known to have numerous side
effects, induce severe withdrawal symptoms and be extremely lethal in overdose. The MAO 
inhibitors are so dangerous that the maintenance of a special diet is necessary to avoid life-threatening
cardiovascular reactions. The minor tranquilizers, like Valium, have also been around for
decades and are probably the most widely prescribed psychiatric medication. Technically,
they are considered apart from the anti-depressants by virtue of
their central nervous system action. Nevertheless, they too are associated with a host of
side effects in addition to being both highly addictive and lethal in combination with other drugs.
The word 'revolution', then, should rightly be reserved for the latest generation of anti-depressants,
the so-called 'selective serotonin reuptake inihibitors' (SSRI's) and their hybrid kin.
These include such brand names as Prozac, Paxil and Zoloft. What is revolutionary about them is
less their mode of action, than the extraordinary media fanfare and scientific claims
accompanying them. Though this is not the first time that a class of
drugs has been alleged to specifically target the presumed biological cause of a
complex psychological function (i.e. depression), they are the first to benefit from the
notion that they might enhance the normal human condition as well. The credibility of both these
claims rests on the theory, widely embraced by the general public, that depression involves a well
defined point source, or sources, in the brain upon which anti-depressant drugs act like magic
bullets surgically targeting the offending region(s). Such a theory, however, seems never to have
been burdened with the facts, for the overwhelming weight of clinical and physical evidence
suggests that the drugs act, not by targeting any hypothetical 'depression center', but by
simply blunting affect and emotion generally. They act, in other words, non-specifically to block
emotional (limbic system) and higher cognitive (frontal lobe) connection. They
don't 'target' anything other than a generalized splitting of
psychic functioning. Indeed, there is a clear line of reasoning that the sine qua non of
their action is precisely their toxicity. In this they are related
to alcohol, the pleasantly delirious effects of which derive largely from its toxicity and
that, likewise, doesn't 'cure' or 'target' any mental dysfunction at all. In fact, a more telling
analogy is to be seen in the comparison with cocaine and amphetamine,
both of whose effects rely, in part, on their inhibition of the reuptake of
serotonin. Ironically, it was cocaine that was first hailed as a
miracle drug and panacea for psychic ills by Sigmund Freud at the turn of the century. That
was until he personally discovered its physically destructive and addictive qualities. The
analogy can be carried further. Both cocaine and amphetamine impact additionally on the dopamine
and adrenergic neurotransmitter systems. So do the SSRI's. Moreover, the claim
that these drugs work functionally and specifically is further belied by the
fact that the serotonin system itself ramifies throughout the brain and spinal cord.
Curiously, in light of the widespread concern about biochemical imbalances in the brain, the
only known such imbalances (apart from a few hormonal conditions like Cushing's syndrome and
Graves' disease) are those caused by the drugs themselves. Lack of appreciation
of this fact leads routinely to travesties in assigning cause and
effect. Thus, the inevitable rebound reactions which ensue upon cessation of medication, are often
interpreted in circular fashion, by doctor and patient alike, as confirming evidence of the
previously hypothesized biological abnormality. It must be
stated at this point, that none of the foregoing is meant to suggest that genes and
biochemistry have nothing at all to do with moods and behaviour.
Nor is it meant to espouse a belief in some sort of metaphysical mind/body dualism. I take it
that the psyche is obviously based in a physical substrate, and that constitutional
factors clearly influence everything from temperament to potential intellectual limits. But to see
biological parameters as framing human potential is a far cry from believing that
we have uncovered - or that there even exist - localized chemical origins of
complex emotional and psychological states. It is, furthermore, naive to suppose that these drugs
could ever act in a functionally specific (i.e. fine tuned) way given
what we know of the complexity of even the most 'primitive' of brain processes (like
temperature and water regulation, for instance). Even
more naive, however, is to suppose that tampering, on a daily basis for perhaps years, even
decades, on end with an organ as delicate and complex as the human brain, is not inherently
dangerous. Certainly our experience with the neuroleptics suggests otherwise. Equally
worrying is that basic biological principles clearly argue for
the potential for permanent changes in physiology when the brain's dynamic homeostasis is
chronically altered or upset. A number of animal studies involving
amplification of the serotonin system have already demonstrated a resulting permanent
loss of serotonin receptors. Also worrying is a recent report in the British medical
journal the Lancet, describing how a group of scientists in the United States had
scanned human brains and found damage to serotonin neurons, caused, they believe,
by the street drug Ecstasy. Studies with monkeys have reinforced these results. Ecstasy is
thought to work, at least in part, by boosting the serotonin system. Statistical Shenanigans Still,
biological psychiatrists will argue, and most people believe, that the SSRI's have undergone a
rigorous battery of independent tests, trials and experimental protocols under the auspices
of the American FDA to insure their efficacy and safety. Nothing could
be further from the truth. First of all, the experimental studies for these drugs are
constructed, financed, and supervised entirely by the drug companies themselves.
Their vaunted independence is a complete myth. Second, the time line of the trials
are so ludicrously short as to fly in the face of the most elementary scientific reasoning.
Prozac, for instance, was released onto the market with only six weeks of clinical trials. In
essence, anyone now taking the drug for more than six weeks is involved in their own study
into its long-term effects. Third, the experimental protocol and statistical
design of many of these studies are a complete scandal in their own right. In the case of Prozac,
among other statistical shenanigans: data were pooled from different sources,
then manipulated into shape; relevant clinical groups were eliminated from participation;
additional confounding medications were administered simultaneous to the test drug; the
dropout rate of roughly 50 percent - and the reasons for - were never factored into the final
results; and, finally, the total number of subjects that actually
finished a placebo-controlled study was a mere 286. It is natural to ask at this point,
why, given their potential danger, we haven't witnessed an epidemic of adverse reactions and
brain damage related to these new generation drugs. As far as the latter effect is
concerned, 'witnessed' is the operative term. The serotonin
neurotransmitter system, unlike the dopamine system upon which the neuroleptics
principally act, is not linked directly to the body's motor system,
therefore any damage that may occur is likely to be much less visible over the short and
intermediate run. Moreover, any emotional scarring or loss that does take place is likely,
again, to be interpreted as part of the original hypothesized
'biological' disorder. That said, it must be noted that the SSRI's do, in fact, also effect
the dopamine and adrenergic systems, and, like the neuroleptics, they can be expected to exert a
malign, if peripheral, influence on these structures as well. Evidence to this effect has
already been documented. Prozac Horror Stories In terms of bad reactions,
the case against the SSRI's is on much firmer clinical ground. Following
its release in 1988, for instance, a flood of Prozac horror stories hit the media. A deluge
of lawsuits quickly followed, whilst Eli Lilly, its manufacturer, embarked on a massive lobbying and propaganda
campaign to protect its $1 billion a year (1993) Prozac market. Among the many pathological
effects that Prozac appeared to induce or exacerbate were: paranoia, compulsion, depression,
suicidal ideation and violence. Numerous bizarre and gratuitous murders and suicides
were credited to its influence, and a number of august journals including the Lancet and the
British National Formulary came out with confirming warnings about 'suicidal ideation'
and 'violent behaviour'. Interestingly, this symptom cluster
is typical of amphetamine psychosis, a, by now, well known result of protracted stimulant
overdose. Like amphetamine, Prozac is functionally a stimulant.
Apart from safety, yet another claim routinely made by proponents of the biological
psychiatric paradigm is that the long term effectiveness of medication for neurotic
disorders is superior to that of traditional psychotherapy. Once again,
a claim with little or no clinical evidence to back it up. Indeed, a number of comprehensive
reviews over the past decade have come out decisively
in favour of psychotherapy. Commonsense would hardly dictate otherwise, for by suggesting to
people that they are merely biologically defective mechanisms capable of handling their
emotional / psychospiritual crises only with the aid of a technological crutch,
many of the fundaments and principles of psychological healing are completely
undermined. Encouraging patients to give up on personal growth and understanding in favour
of pills, is, apart from being a philosophy of despair, a recipe for emotional disaster. Thus,
helplessness is substituted for mastery, dependency for autonomy,
and an unexamined life takes the place of self-discovery. Moreover, at precisely the
time of greatest need, the patient-cum-pscyhic adventurer is delivered up to a zombie-like state
devoid of both mental acuity, and the capacity for deep feeling,
self-awareness and self-empathy. That biological psychiatry could so blithely trample
underfoot such granite pillars of therapeutic commonsense is chilling. Even more chilling
is the fact that the biological paradigm has expanded well beyond the confines of the adult
population. For though most medicated adult patients can be said
to be nominally voluntary, medicated children can in no way be so considered. It is curious
that, in an era deluged with an avalanche of new statistics detailing the pervasiveness of
childhood poverty, neglect, and abuse, the psychiatric profession has chosen to ignore the obvious
psychsocial causes of most childhood behavioural disorders
and has opted, instead, to crusade for the wholesale drugging of this involuntary population
on the basis of totally unsubstantiated theories of biological causation. Thus, there is
hardly a shred of experimental evidence to buttress such trendy childhood
'disease' entities as Minimal Brain Dysfunction, Learning Disorder, or
Attention-Deficit Hyperactivity Disorder. No underlying local
organic malformation, physiological malfunction or chemical basis has ever been clearly
demonstrated for these syndromes and no well controlled clinical studies have ever
unequivocally supported them either. This has not stopped the
escalating prescription of such stimulants as Ritalin and Dexedrine despite a host of
negative side effects including, tics, spasms. growth suppression, and chronically elevated heart
rates and blood pressure. Increasingly, Prozac is also being given to children
despite their never having been part of the original experimental protocol. The license
for such practice derives from the fact that, once the FDA has approved a drug, there are few
restrictions on how or to whom a doctor can prescribe it. In line with this practice, the anti-depressants
in general have become a jack-of-all-trades medication prescribed for everything from insomnia
to migraine headache. In stark contrast to this massive, state sanctioned drug laundering
operation is the harshly punitive 'war' the state wages against illegal drugs.
Though beyond the scope of the present discussion, this fascinating
paradox points up the concluding need to briefly confront
some of the broader social implications of the biological psychiatric paradigm. A Biased
Conception Of What It Means To Be Human As part of its general
philosophical stance this paradigm is a conceptual formation with an implicit, highly
ideological portrayal of the nature of 'human nature'.
In this sense it is aimed at us all, for at the heart of any political philosophy will be found
a biased conception of what it means to be human. Culturally, the notion that we should conceive
ourselves primarily as biochemical mechanisms is not only dangerously dehumanizing and
spiritually stunting, it leads inevitably to both a dismissive and escapist attitude towards many
genuinely psychological and social problems. In having suborned, in other words, a substantial
proportion of the population into believing their behaviours are
dictated principally by their genes and their biochemistry, biological psychiatry has not only
set back the psychological paradigm a hundred years, it has also fanned the flames of a simplistic,
reductionist view of human nature and of human society. Possessed by the reductionist
daemon, psychiatry today, remains blind to its own historical contingency,
to its own social, cultural, economic and political conditioning. Unable
to see that it too has a case history, it remains insensible
to its own, quite advanced pathology.
Canadian Dimension, 2B-91 Albert Street, Winnipeg, Manitoba, Canada, R3B 1G5
Subscription Hot Line: 1-800-737-7051