Re: US legislation question
Posted: Mon Oct 13, 2003 7:33 pm
Hi all,
I'm trying to understand some literature I've gotten in the mail and from
health food stores about some proposed US legislation, and wondering if
anyone can give me insight. This is re S. 722 ("This bill would subject
nearly all vitamins, minerals, herbal products and other supplements to a
level of scrutiny that is both unwarranted and unnecessary. Products ...
would be subject to clinical evaluation using standards that are at the
complete discretion of the FDA...."), and its proposed alternative, S. 1538
("No more excuses from the Food and Drug Administration! Give the FDA the
resources it needs to implement DSHEA!"). Evidently S. 722 has some quite
nasty restrictions written into it, such as the FDA's right to withdraw any
dietary supplement for which *even one* adverse reaction is reported. (What
if they applied that standard to pharmaceuticals?)
But its proposed alternative doesn't sound great to me either. Taken from
capwiz.com/nnfa/issues/alert/?alertid=3098131&type=CO, description of that
bill begins:
"SUPPORT S. 1538
"No more excuses from the Food and Drug Administration! Give the FDA the
resources it needs to implement DSHEA!
This bill will eliminate the Food and Drug Administration's favorite excuses
that it doesn't have enought staff, money or power to regulate supplements.
The FDA has fallen short when it comes to enforcing the law."
(continues with an explanation of why food supplements are better than
drugs)
Why do we want the FDA to have more staff and more money, and why do we want
them overseeing non-pharmaceutical products? I hear so many horrible things
about that agency and their apparent collaboration with pharmaceutical
companies, that I sort of shudder at the idea of giving them more rope to
work with.
Can anyone shed more light on this for me?
Neurotically,
Shannon
I'm trying to understand some literature I've gotten in the mail and from
health food stores about some proposed US legislation, and wondering if
anyone can give me insight. This is re S. 722 ("This bill would subject
nearly all vitamins, minerals, herbal products and other supplements to a
level of scrutiny that is both unwarranted and unnecessary. Products ...
would be subject to clinical evaluation using standards that are at the
complete discretion of the FDA...."), and its proposed alternative, S. 1538
("No more excuses from the Food and Drug Administration! Give the FDA the
resources it needs to implement DSHEA!"). Evidently S. 722 has some quite
nasty restrictions written into it, such as the FDA's right to withdraw any
dietary supplement for which *even one* adverse reaction is reported. (What
if they applied that standard to pharmaceuticals?)
But its proposed alternative doesn't sound great to me either. Taken from
capwiz.com/nnfa/issues/alert/?alertid=3098131&type=CO, description of that
bill begins:
"SUPPORT S. 1538
"No more excuses from the Food and Drug Administration! Give the FDA the
resources it needs to implement DSHEA!
This bill will eliminate the Food and Drug Administration's favorite excuses
that it doesn't have enought staff, money or power to regulate supplements.
The FDA has fallen short when it comes to enforcing the law."
(continues with an explanation of why food supplements are better than
drugs)
Why do we want the FDA to have more staff and more money, and why do we want
them overseeing non-pharmaceutical products? I hear so many horrible things
about that agency and their apparent collaboration with pharmaceutical
companies, that I sort of shudder at the idea of giving them more rope to
work with.
Can anyone shed more light on this for me?
Neurotically,
Shannon