Open letter from European medical associations to Members of the
European Parliament
7 June 2000
On May 25, the Environment and Public Health Committee of the European
Parliament adopted a report by Jules Maaten MEP on a proposed EU
Directive to strengthen regulations on the manufacture, presentation
and sale of tobacco products. As representatives of Europe's doctors,
we believe that regulation of tobacco must reflect the true nature
of the health risks. We therefore address this open letter to
all Members of the European Parliament, urging them to make the
health of Europe's citizens their first priority by supporting the
Maaten report at the plenary session on 12-15 June in Strasbourg.
Every day, European doctors come face to face with the suffering
and death caused by tobacco. In the EU alone in 1990, more than
half a million people died as a result of their tobacco use. The
measures proposed in the Maaten report will go some way towards
reducing this terrible toll.
Nicotine addiction is the main motivating force behind tobacco
use. Tar is a potent cocktail of cancer-causing substances, and
carbon monoxide is a major contributor to diseases of the heart
and circulation. The Directive recommends reducing the tar content
of cigarettes and introducing limits on carbon monoxide and nicotine.
More than 600 additives are licensed for use in tobacco products.
We believe that smokers have the right to know what they are
consuming, and support the proposal to require the disclosure
and testing of these substances.
Smokers have the right to full and accurate information on the
health risks of tobacco. Health warnings are an important source
of information, and are particularly effective in reaching young
people and those wishing to quit. Research shows that the larger
the health warning, the more effective it is. We support the proposal
that the health warning should cover 40% of the front of the pack,
and 50% of the back. An expert committee should be established to
identify messages that are effective.
Under the Directive, use of terms such as 'light', 'mild', and
'ultra-light' will be prohibited throughout the EU. These terms
mislead smokers into thinking such products are less harmful, when
there is evidence that precisely the opposite may be true.
Finally, we urge members of parliament to ensure that the Directive
applies to all tobacco products manufactured and sold in the EU.
Products for export often find their way back into the European
market. Moreover, there can be no scientific or ethical basis
for perpetuating double-standards that deny minimum standards
of protection to consumers in the accession states and elsewhere.
The proposed directive presents an important opportunity for members
of the European Parliament to protect European consumers from a
product that is uniquely hazardous to health. We call upon the European
Parliament to give priority to the health of Europe's citizens
by voting for a robust Directive on the manufacture, sale and presentation
of tobacco products.
Yours sincerely,
Dr Reiner Brettenthaler
Vice-President, Austrian Medical Association
Dr Roland Lemye
Secretary-General for International Affairs
Belgian Association of Medical Unions
Dr Mac Armstrong
Secretary
British Medical Association
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