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2001/06/01 -Two major elements of the current tobacco settlement proposal will require substantial revision for the
agreement to
succeed in its most important potential benefit to public health
--
reducing smoking rates and therefore tobacco-caused disease and
death,
according to the American Cancer Society (ACS).
"There are many questions about this proposal that still need to
be
answered," said ACS President Myles Cunningham, MD, "but before
the
American Cancer Society can even consider supporting a
settlement plan,
we hope Congress will assure legislation which requires: (1)
absolute
assurance that the FDA will have complete and unfettered
authority over the
regulation of nicotine and other cigarette ingredients, and (2)
a
significant strengthening of tobacco industry penalties for
failure to
reach smoking rate reduction goals set in the settlement's
"look-back"
provision."
"While the American Cancer Society still believes at this point
that a
settlement agreement with tobacco companies has more potential
for
advancing public health than the uncertain outcome of lengthy
continued
litigation or piecemeal legislation, these two troublesome
settlement
elements could cancel out the progress we could make with the
other
industry concessions," Dr. Cunningham said.
"It is our goal to help influence a final resolution that allows
society to
make a quantum leap in public health," said ACS Board of
Directors Chairman
George Dessart. "We have not yet completed our evaluation of
the
settlement document and will not take a final positive position
until we
are convinced we have a blueprint that leads us to that result.
In the
meantime, we hope to assist in the Congressional review of this
issue by
furnishing background information on what we perceive to be the
settlement's implications on public health.
"We have noted that language in the settlement document places
restrictive
burdens on FDA's ability to regulate nicotine and other cigarette
ingredients," said Dr. Cunningham. The settlement document
requires that
FDA present a "preponderance of evidence" that such
ingredients are
harmful to health and that restricting them would not create a
black
market. "These restrictions contradict the rules by which FDA
may
regulate any other substance under its jurisdiction," said Dr.
Cunningham.
"It is absurd and unacceptable to create a standard that is more
burdensome
on FDA authority on products as deadly as these. FDA's
jurisdiction over
tobacco products has been upheld by the Greensboro Federal Court
decision.
There is no logical basis for backtracking on that victory here,
when what
we really want is legislation which guarantees it."
ACS's initial evaluation of the settlement language has also
noted that
there appears to be an insufficient incentive for tobacco
companies to
achieve the reduction in youth smoking rates prescribed by the
settlement
plan, according to George Dessart. "It needs to be so
financially painful
for the industry to miss these 30% and 60% decreases in youth
smoking rates
at five and ten years respectively, that working hard to achieve
them is
their only option," he said.
"We believe that tobacco industry concessions on advertising
bans, warning
labels and public education are creating a potential for
significant
progress toward a society free of tobacco-caused disease and
death," said
Dessart. "But this opportunity is too important for fast
responses. The
longer we look at this, the more we realize how crucial it is
that we have
a full public and Congressional evaluation of these important
plan
elements. "
Joann Schellenbach
National Director Media Relations
American Cancer Society
212-382-2169
jschelle@cancer.org
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