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US: Opinion: Why Won't Government Let Us Use Marijuana As Medicine?

Boston Globe (MA)

Thursday 07 Dec 2000

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Website: http://www.boston.com/globe/
Author: Dr. Lester Grinspoon, professor emeritus at Harvard Medical
School, is the author of "Marihuana Reconsidered" and "Marihuana, the
Forbidden Medicine."




HIGH-RANKING government officials in the United States have referred to
the concept of medical marijuana as a hoax, a subterfuge by which
proponents of a more liberal policy toward this drug will succeed in
undoing the long-standing, harsh prohibition.

Ignorant of the role cannabis played in Western medicine from mid-19th
into the early 20th century, they and their many supporters view the
notion that cannabis has medicinal properties as a new intrusion into
allopathic medicine. The parochialism of this view is highlighted by
ethnohistorical studies which document not only how ancient is the use
of this substance as a medicine but, as well, the multiplicity of
cultures that have used it in so many different ways for the treatment
of a large variety of human ailments and discomforts.

Its use as a medicine is so widespread and reports of its toxicity so
rare, the contemporary judgment of Western medicine seems deviant. One
might ask why the government of the United States, the leading
oppositional force, clings so tenaciously to this insular and harmful
policy?

The answer, of course, is the fear that as people gain more experience
with cannabis as a medicine they will discover that its toxicity has
been greatly exaggerated, its usefulness undervalued, and that it can be
used for purposes the government disapproves of. Having made these
discoveries, they will be less supportive of the prohibition and its
enormous costs, among which is the annual arrest of 700,000 people in
the United States alone.

With the publication of its report in March 1999, the Institute of
Medicine of the National Academy of Sciences grudgingly acknowledged
that cannabis has some medical utility but averred that because smoking
it was too dangerous to their health, patients would have to await the
development of pharmaceutical products that would eliminate this hazard.

While the report greatly exaggerates the danger of smoking cannabis, it
fails to provide a discussion of vaporization, a technique that allows
patients who wish to avoid the smoke to inhale the cannabinoids largely
free of particulate matter.

Another reason the authorities would have patients wait for the
"pharmaceuticalization" of marijuana is to allow for the development of
cannabinoid analogs that will be free of any psychoactive effects.

This goal is based on the assumption that the psychoactive effects are
both unhealthy and bad for the patient in the vague way in which the
"high" is thought by the prohibitionists to be deleterious.

It is an assumption that is not supported by the mountain of anecdotal
evidence that supports marijuana's usefulness as a medicine. While
there are some patients who do not like the psychoactive effects, they
are relatively rare; the vast majority, patients suffering from serious
illnesses, finds that smoking cannabis not only relieves a particular
symptom, but also makes them "feel better."

Helping patients, particularly those with chronic diseases, feel better
is an important goal of the humane practice of medicine. And there is a
growing understanding in medicine that patients who feel better do
better.

The resistance of government authorities to allowing the availability of
cannabis as a medicine is generally supported by the Western medical
establishment. This has not always been so. Physicians in the United
States were enthusiastic about the medicinal uses of cannabis from the
middle of the 19th century until the passage of the first of the
Draconian legislation aimed at marijuana in 1937 (the Marijuana Tax
Act).

Under pressure from the Federal Bureau of Narcotics, the predecessor
organization to the present Drug Enforcement Administration, the Journal
of the American Medical Association published in 1945 a vehemently
antimarijuana editorial, which signaled a sea change in the attitude of
doctors toward this drug. They became both victims and agents of the
marijuana disinformation campaign launched by Harry Anslinger, the first
chief of the Federal Bureau of Narcotics.

Many physicians still suffer from both this legacy and fear of the DEA,
so much so that they are afraid to prescribe Marinol (a legally
available synthetic THC, both more expensive and less effective than
marijuana).

Today, the medical establishment takes the position that there is no
scientific evidence demonstrating that cannabis has medical usefulness.
This stance is based on the fact that there is a paucity of double-blind
controlled studies of the clinical usefulness of marijuana.

This scarcity is likely to persist for some time. The costs of such
studies are generally underwritten by pharmaceutical firms that stand to
gain much if they can demonstrate a therapeutic usefulness in, and win
Food and Drug Administration approval of, a drug whose patent they hold.
Because this naturally occurring herb can not be patented, these firms
will not invest the more than $200 million needed to do the studies
required for official approval of a pharmaceutical. Consequently, the
medical utility of marijuana will continue to rest on anecdotal
evidence.

It would not be the first medicine to be admitted to the pharmacopoeia
on the strength of anecdotal evidence. Anecdotal evidence commands much
less attention then it once did, yet it is the source of much of our
knowledge of synthetic medicines as well as plant derivatives.
Controlled experiments were not needed to recognize the therapeutic
potential of chloral hydrate, barbiturates, aspirin, curare, insulin, or
penicillin.

It is unlikely that marijuana will ever be developed as an officially
recognized medicine via the FDA approval process, which is ultimately a
risk/benefit analysis. Thousands of years of widespread use have
demonstrated its medical value; the extensive multi-million dollar
government-supported effort (through the National Institute of Drug
Abuse) of the last three decades to establish a sufficient level of
toxicity to support prohibition has instead provided a record of safety
that is more compelling than that of most approved medicines.

The modern FDA protocol is not necessary to establish a risk-benefit
estimate for a drug with such a history. To impose this protocol on
cannabis would be like making the same demand of aspirin, which was
accepted as a medicine more than 60 years before the advent of the
double-blind controlled study.

Many years of experience have shown us that aspirin has many uses and
limited toxicity, yet today it could not be marshalled through the FDA
approval process. The patent has long since expired, and with it the
incentive to underwrite the enormous cost of this modern seal of
approval.

Cannabis too is unpatentable, so the only source of funding for a
"start-from-scratch" approval would be the government. Other reasons
for doubting that marijuana would ever be officially approved are
today's antismoking climate and, most important, the widespread use of
cannabis for purposes disapproved of by the US government. As a result,
we are going to have two distribution systems for medical cannabis.

One will be the conventional model of pharmacy-filled prescriptions for
FDA-approved medicines derived from cannabis as isolated or synthetic
cannabinoids and cannabinoid analogs. The other will have more in
common with some of the means of distribution and use of alternative and
herbal medicines. The only difference, an enormous one, will be the
continued illegality of whole smoked or ingested cannabis.

In any case, increasing medical use by either distribution pathway will
inevitably make growing numbers of people familiar with cannabis and its
derivatives.

As they learn that its harmfulness has been greatly exaggerated and its
usefulness underestimated, the pressure will increase for drastic change
in the way we as a society deal with this drug.


 

 

 

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