| |
What
is the ACMD's statutory duty under the Misuse of
Drugs Act?
The
ACMD have a statutory duty to advise Government
about:
risk
assessments of harmful drug use
regulatory
assessments to prevent harmful drug use
ways
to restrict availability of harmful drugs and
regulate their supply
advice,
treatment and after-care required by those
affected by harmful drug use
ways
to enhance cooperation to tackle harmful drug
use
education
of the public, especially the young, about
harmful drug use
research
required to help prevent harmful drug use
Why
does the ACMD use the word 'drugs' to only mean
illegal drugs, contradicting the use of the word in
the MDA?
There
is no exclusion clause in the MDA for the traditional
drugs alcohol and tobacco. They are harmful drugs in
every way that illegal drugs are. However the ACMD do
not refer to them as drugs, instead using 'drugs' to
mean only illegal drugs. Under Section 2 illegal
drugs are referred to as 'controlled drugs' not
'drugs'. The ACMD's inaccurate use of the word
'drugs' leads to many inaccurate statements. This
fundamentally contradicts their duty to provide
advice about drug education: they imply alcohol and
tobacco are not drugs.
Under
the National Curriculum all children are
taught at school that alcohol and tobacco are
drugs. The Department for Education and
Skills' Drugs: Guidance
for schools [para 1.3] says "The
definition of a drug given by the United
Nations Office on Drugs and Crime is: a
substance people take to change the way they
feel, think or behave. The term
drugs and drug
education, unless otherwise stated, is
used throughout this document to refer to all
drugs: all illegal drugs (those controlled
under the Misuse of Drugs Act 1971), all
legal drugs, including alcohol,
tobacco".
The
United Nations
definition of 'drugs' [chap 2 , p.1]:
"What are drugs? A very basic question
but one that needs to be clarified. For, if
we start thinking of drugs as just the
substances that cause problems or are abused
by people we know, then we are likely to
ignore other substances that, for one reason
or another, are not thought of as drugs by
our immediate communities. A psychoactive
substance is any substance people take to
change either the way they feel, think, or
behave. This description covers alcohol and
tobacco as well as other natural and
manufactured drugs".
Home
Office guidance: The Home Office/DPAS
publication Let's Get Real -
communicating with the public about drugs [p.40] says "in
the interests of encouraging a rational
debate and combating knee-jerk prejudice, we
need to continue referring to alcohol,
tobacco and caffeine as drugs".
The
Government's Talk to Frank drug
education website says "drugs are
illegal" but then states that "tobacco comes
from the leaves of the tobacco plant. It
contains a drug called nicotine which is
highly addictive".
The
ACMD have advised Government about the
harmful use of medicinal drugs, legal
substances (e.g. volatile substances) as well
as illegal drugs so clearly they do not
believe their duty is restricted to illegal
drugs. For example, "Along with
seven other drugs, Gammahydroxybutrate (GHB)
will become controlled under the Misuse of
Drugs Act 1971, after the Advisory Council on
the Misuse of Drugs (ACMD) recognised that it
was being widely misused and has harmful
effects. GHB is a drug developed as an
anaesthetic".
Why
doesn't the ACMD advise Government about the drugs
alcohol, tobacco and caffeine?
The
ACMD Secretariat has told us "Whilst it
can be argued that the ACMD has a remit to
consider alcohol, tobacco and caffeine it
has, to date, declined to do so. The ACMD
consider that its resources are best served
by focussing on controlled drugs or drugs
likely to be controlled by the MDA 1971.
Albeit independent, the ACMD as an advisory
body has to be aware of the Governments
position, which has not given any intention
to consider the control of alcohol, tobacco
and caffeine".
Caroline
Flint, Home Office drugs minister, has told
us that "alcohol, tobacco and caffeine
will not be considered by the ACMD for
control". The Home Office's Chief
Scientific Adviser, Professor Wiles, has
assurred me that this only means the
Government will not ask the ACMD to advise
about these drugs rather than actively
preventing them from doing so. However
neither the ACMD Secretariat nor Professor
Wiles have answered these questions I have
asked: Why does an independent scientific
committee focus its inevitably limited
resources "on controlled drugs or drugs
likely to be controlled" - in accordance
with the current governments Drugs
Strategy - rather than on the most harmful
drugs in accordance with objective
scientific evidence and, I believe, with
their statutory duty? How did the ACMD decide
that they have the legal authority to limit
their statutory duty in such a way? Did the
ACMD discuss this decision with the Home
Office? Did the ACMD consider alternatives
such as requesting sufficient resources to
advise on all potentially harmful drugs? Did
the ACMD consider any unintended consequences
of their decision such as their consequent
inability to assess the relative harms of the
intoxicant drugs alcohol and cannabis?
See our personal correspondence with the ACMD
and Home Office here. More on the importance of
independence and sufficient resources in
scientific advice provision here.
The
Government has a conflict of interest:
alcohol and tobacco may cause a fifth of all
deaths but ninety percent of voters consume
them and Government receives £20 billion a
year in taxation from their trade. Government
may be putting their own interests, job
prospects and drug profits, before the public
interest, public health considerations.
Risk
familiarity affects the risk tolerance of
Government, ACMD and public: familiar risks
(e.g. traditional drugs) are underestimated
and unfamiliar risks (e.g. non-traditional
drugs) are overestimated. Regulations are
proportionate to risk tolerance, not to the
scientific evidence of risk of drug harm.
Traditional drugs are just as harmful as
non-traditional drugs.
The Government's drug
education website Talk to Frank
warns of this bias to risk perception
saying "alcohol
can play a major part in many
people's social lives. That's why
it's easy to forget that it's
actually a very powerful drug".
The United
Nations [chap 2 , p.1] is
also concerned about the effect
saying "if we start thinking of
drugs as just the substances that
cause problems or are abused by
people we know, then we are likely to
ignore other substances that, for one
reason or another, are not thought of
as drugs by our immediate
communities. A psychoactive substance
is any substance people take to
change either the way they feel,
think, or behave. This description
covers alcohol and tobacco as well as
other natural and manufactured
drugs".
The Parliamentary
Office of Science and Technology
leaflet Safety in
Numbers [p.2] describes
factors affecting risk perception
saying "Familiarity
People appear to be more willing to
accept risks that are familiar rather
than new risks".
The Department of
Healths Communicating
about risks to public health says
"Risks are generally more
worrying (and less acceptable) if
perceived to arise from an unfamiliar
or novel source".
The ACMD's failure to
provide consistent advice for all
harmful drug use contradicts the
Better Regulation Task Force's
principle of Consistency in their Principles
of Good Regulation. BRTF
say "regulators should be
consistent with each other, and work
together in a joined-up way" but
the regulatory advice the ACMD
provide about non-traditional drugs
is not consistent with traditional
drug regulations. Traditional drug
consumption, trade and production is
regulated to tolerate reasonably safe
drug use, educate against drug use
harmful to the consumer, legislate
against drug use harmful to others
and to allow taxation of the trade to
pay for all drug-related services.
Non-traditional drug consumption,
trade and production is prohibited
resulting in the demand being met by
the unregulated black market. As a
result all non-traditional drug
profits go to organised crime leaving
the general taxpayer to cover the
cost of drug-related services.
Why
isn't the ACMD's advice targeted at harmful drug use
instead of all drug use?
The
ACMD's statutory duty only applies to harmful
drug use, not all drug use. They have a duty
then to define the boundary between harmful
drug use and reasonably safe drug use, if
such use exists. Their advice must then be
targeted only at harmful drug use.
The
ACMD interpret the word harmful to mean 'not
harmless'. Under such a definition all
activities are harmful and the word loses its
meaning. No medicinal drug is harmless, all
have side-effects. The intention of the MDA
is to prevent unreasonably harmful drug use.
The ACMD's report The
Classification of cannabis under the MDA [para. 5.1] says
"the high use of cannabis is not
associated with major health problems for the
individual or society" but they
recommend continued prohibition because
"cannabis is not a harmless substance
and its use unquestionably poses risks both
to individual health and to society".
The ACMD Chairman wrote a letter to The Times saying "the
classification system for drugs does not mean
that any of these substances are harmless. If
they were, they would not be included in the
Misuse of Drugs Act". The Chairman seems
to suggest that harmless drugs exist and even
that alcohol and tobacco may be harmless as
these drugs are not included in the Misuse of
Drugs Act. The Strategy Unit's Risk: improving
government's capability to handle risk and
uncertainty [para. 5.29] says "A
number of Departments we spoke to said that a
widespread lack of understanding about basic
risk concepts sometimes made it difficult for
them to conduct an informed public debate
about risks. The most frequent areas of
concern were low levels of awareness about
probabilities leading to disproportionate
levels of concern about high-impact,
low-probability risks and a reluctance to
accept that no activity could be entirely
risk free". The ACMD seems reluctant
"to accept that no activity could be
entirely risk free".
The
ACMD's failure to target their advice at the
problem, harmful drug use, contradicts the
Better Regulation Task Force's principle of
Targeting in their Principles of
Good Regulation. BRTF say
"regulation should be focused on the
problem, and minimise side effects".
Failure to target regulation at the problem
results in unintended consequences.
Reasonably safe drug use is prohibited as
well as harmful drug use. As a result many
people refuse to comply with a law that
prevents them from persuing a reasonably safe
activity so demand remains high and supply is
met by the black market instead, an
unintended consequence.
Why
doesn't the ACMD's advice discriminate between drug
use harmful to the consumer and drug use harmful to
others?
Risk
guidelines discriminate between the voluntary
risk of self-harm and the risk of imposing
harm on others; education is the appropriate
intervention to reduce the risk of self-harm
while legislation is appropriate to prevent
the risk of harm to others.
The Strategy Unit's Risk:
improving government's capability to
handle risk and uncertainty says
"the risks that the public faces
may be voluntarily undertaken (for
example, smoking or dangerous
sports), with greater or lesser
degrees of awareness of the risk, or
imposed by other individuals or
organisations" and
"governments will not normally
intervene where individuals take
risks voluntarily and where they
alone are affected. In these
circumstances, governments have a
role in ensuring that individuals are
aware of their responsibility and of
the consequences of the risk that
they are taking".
The Cabinet Office/HM
Treasury risk guidance, Principles
of managing risks to the public, says:
"Responsibility: Government will
seek to allocate responsibility for
managing risks to those best placed
to control them. It will consider the
need to regulate where risks are
imposed on others. It will aim to
give individuals a choice in how to
manage risks that affect them, where
this does not expose others to
unacceptable risk or cost".
The Health and Safety
Executive's Taking
account of societal concerns about
risk says "judgements
about risk are very powerfully
influenced by whether they are seen
as voluntary or imposed" and
"attempts to criminalise
self-risk usually have undesirable
consequences". It goes on to say
"the freedom to control events
in one's life is itself a jealously
guarded reward. Impositions that
infringe this freedom - whether in
the form of regulations or risks are
likely to encounter opposition"
and "imposed saftey can be
resented as strongly as imposed
risk".
Individual
responsibility for health choices:
the Government's Saving
lives: our healthier nation [para. 3.25]
says "it is the role of the
Government to provide information
about risk. But in most cases it is
for the individual to decide whether
to take the risk. And there is also a
balance between risk and personal
freedom. Some people enjoy pursuing
outdoor sports which others would
consider too dangerous to undertake.
As long as people are aware of the
risk which they are taking, it is
their decision whether to put
themselves at risk".
The Department of
Health's Wanless report Securing
good health for the whole population says
"Individuals must be free to
make their own choices about their
own lifestyles. If government or
other bodies do intervene, it is
essential that social welfare is
improved and that personal freedoms
are respected".
"Influencing and, over time,
changing social attitudes to health
and lifestyles is likely to be much
more effective in the long run than a
punitive approach that does not also
aim for a change in attitude. Laws
and regulations not accompanied by
public support incur high enforcement
costs, and could jeopardise the
development of a consensus for future
public health measures".
"It is important that any
government intervention is well
managed, to protect against an
inappropriate infringement of liberty
or unintended consequences".
"Where regulation is enacted, it
is important that it is both
efficient and respects civil
liberties". "Limits to
Government intervention:
Interventions to improve public
health have the potential to reduce
significantly personal freedoms. This
is most clear when government acts
explicitly to prevent or restrict
individuals from behaving in certain
ways, or from consuming particular
goods. In general, if the freedom to
be curtailed or limited is a
significant one and valued highly by
the individual, the state would need
strong reasons to impose its will
over the individual on public health
grounds. Usually, there should at
least be a strong consensus,
preferably public but certainly
professional, that the public health
measure is necessary to prevent harm
to others. Government can of course
legitimately intervene when
ones freedom to act would
infringe human rights for example, a
person with a highly infectious
disease may need to be quarantined
without consent. In other cases,
however, the mere fact of social or
professional consensus may not
provide sufficient justification for
action". "it is important
to recognise that measures should be
justifiable in the public interest
and to individuals as a reasonable
restriction of their freedom".
The Strategy Unit's Personal
responsibility and changing behaviour [para. 3.5]
says "the eventual aim is to
entrench a habit of personal
responsibility and restraint, and a
self-sustaining social norm".
"For many traditions of social
and political thought greater
personal responsibility is a good in
itself: it enables society to
function with a less coercive state
and judicial system; it enables
public goods to be provided with a
lower tax burden; the exercise of
responsibility strengthens individual
character and moral capacity; and
greater personal responsibility
in terms of restraint and
support for others enhances
the quality of life of the whole
community". "All modern
societies suffer the consequences of
prohibitions that are only partially
effective for example, against
hard drug use. Clearly laws on their
own have only limited efficacy where
other powerful drivers of behaviour
are involved. There is a mature and
growing body of knowledge in
psychology offering a more
sophisticated approach to behaviour
and behaviour change, but that
remains largely untapped by many
policymakers".
"interventions to curb drug use
have been popularly supported despite
relatively modest evidence of
significant impact". "An
over-arching logic: helping people
help themselves: ... policy must at
once empower and give choices, but at
the same time policy should set the
default to be in the best interests
of individuals and the wider public
interest. To be effective, this twin
approach needs to be built around a
sense of partnership between state
and individual. Hence in employment,
while individuals are not ultimately
forced to work, the strong default
pressures are that they will. In
education, young people are not
forced to stay on in school and
acquire qualifications, but the
default pressures are that this is
what they do. And in health,
governments do not ban unhealthy
foods or smoking, but seek to
refashion the behavioural pressures
towards healthier choices".
The
ACMD's failure to target education at the
voluntary risk of self-harm and legislation
only at the risk of imposing harm on others
contradicts the Better Regulation Task
Force's principle of Proportionality in their
Principles of
Good Regulation. BRTF say
"Regulators should only intervene when
necessary. Remedies should be appropriate to
the risk posed" and "enforcers
should consider an educational, rather than a
punitive approach where possible".
Harm
to others: consumers impose risks on the
public - e.g. drug driving, passive smoking
and fire risk; suppliers impose risks on
consumers - advertising and sales to young
people; producers impose risks on consumers -
lack of quantity and quality control and lack
of health warnings; and the whole drug trade
imposes costs on society - the cost of
drug-related services, education, treatment
and legislation; Government intervention
imposes costs on all - e.g. imposing a risk
of social exclusion and punishment on those
who harm no-one else, an economic risk to the
tax payer to pay for enforcement, an economic
and health risk to society by denying
competition between drugs (e.g alcohol v
cannabis) and denying informed choice to
consumers.
Why
do the ACMD recommend punishment out of proportion to
risk?
The
ACMD's report The
Classification of cannabis under the MDA [para. 6.2]
recommended reclassifying cannabis from Class
B to Class C on the basis of proportionality
of regulation to risk. The report says
"Cannabis, however, is less harmful than
other substances within Class B. The
continuing juxtaposition of cannabis with
these more harmful Class B drugs erroneously
(and dangerously) suggests that their harmful
effects are equivalent. This may lead to the
belief, amongst cannabis users, that if they
have had no harmful effects from cannabis
then other Class B substances will be equally
safe". However the report also compares
cannabis to alcohol and tobacco in terms of
likelihood of taking risks, risk of accident,
of violence, of respiratory depression, of
cancer, of harming pregnancy and of taking
other drugs: in all cases cannabis is said to
be safer or no more harmful. Why recommend
continued prohibition of a safer alternative
to alcohol and tobacco when they are aware of
the dangers of disproportionate laws? The
Government's Updated Drug
Strategy 2002 [p.22] points out the dangers
again saying "it is vital that the
Government's message to young people is open,
honest and credible. Drug laws must
accurately reflect the relative harms of
different drugs if they are to persuade young
people in particular of the dangers of
misusing drugs". Quite.
The
ACMD's failure to provide regulatory advice
proportionate to risk contradicts the Better
Regulation Task Force's principle of
Proportionality in their Principles of
Good Regulation. BRTF say
"Regulators should only intervene when
necessary. Remedies should be appropriate to
the risk posed" and "enforcers
should consider an educational, rather than a
punitive approach where possible".
If
regulations were proportionate to risk we
would expect to see obvious evidence that
illegal drugs are very considerably more
harmful then legal drugs. Drug dealers may
supply a drug that warns it kills, tobacco,
alongside sweets for children in 200,000
outlets around the UK, but if they sell
illegal drugs they are imprisoned for years.
In fact there is no evidence that even heroin
is more harmful than tobacco and alcohol. It
is quite possible to be a heroin addict all
one's life and suffer no harmful
consequences. See the World Health
Organisation's comparison of drug prevalence
and harm here.
In providing
regulatory advice does the ACMD clearly distinguish
between the roles of scientific evidence about drug
risk and regulation, public opinion, Government
policy and international law?
The Code of
Practise for Scientific Committees says "13.
Where a committee is required to offer advice on
social, ethical and economic considerations which
bear on the scientific advice, it should be made
explicit to the committee that this role is being
taken on". The ACMD's statutory duty is
clearly laid out by law, the MDA, and should take
account of these factors - but none are
mentioned.
|