So maybe we should get rid of the FDA and let pharma release whatever drugs they want to and rely on reports of bad side effects up to and including deaths be voulntarily reported by people who have to then try to go to court and sue to get any bad ones removed from the market. Fewer people should die that way than with the FDA around, right? A "free market solution" to regulations? Remember when companies were caught posing as customers and posting positive reviews of their own products on sites including Amazon? Surely that can't happen again! The people will have deep pockets to file and fight these lawsuits against those puny companies, right?
Sure the FDA, which is made up of people, is not perfect. No human enterprise is. But it would be scary to consider what things might be like without them out there.
Would any private testing company be any more or less susceptable to influence from drug companies than the FDA? What would prevent that? Would they have the resources to do reliable testing on drugs including blind studies? Where would they get the money to do the testing? Maybe from drug company contributions?
You don't need to be a scientist to know if something works for a condition.
So maybe we should get rid of the FDA and let pharma release whatever drugs they want to and rely on reports of bad side effects up to and including deaths be voulntarily reported by people who have to then try to go to court and sue to get any bad ones removed from the market. Fewer people should die that way than with the FDA around, right? A "free market solution" to regulations? Remember when companies were caught posing as customers and posting positive reviews of their own products on sites including Amazon? Surely that can't happen again! The people will have deep pockets to file and fight these lawsuits against those puny companies, right?
Sure the FDA, which is made up of people, is not perfect. No human enterprise is. But it would be scary to consider what things might be like without them out there.
Would any private testing company be any more or less susceptable to influence from drug companies than the FDA? What would prevent that? Would they have the resources to do reliable testing on drugs including blind studies? Where would they get the money to do the testing? Maybe from drug company contributions?
Bull, even the doctors have to engage in trial and error, and if you want to be safe you get all your scrips filled at the same pharmacy and go over side effects with the pharmacist on each new prescription because they know more than the doctors.
Many conditions can not be controlled with diet and exercise - diabetes, asthma and COPD, some heart and blood pressure problems, many more.
This discussion puts the GROSS in gross over simplification.
Bull, even the doctors have to engage in trial and error, and if you want to be safe you get all your scrips filled at the same pharmacy and go over side effects with the pharmacist on each new prescription because they know more than the doctors.
Unfortunately your vision of the FDA is an unworkable fantasy. It will always be controlled by corporations by the very nature of its existence.
BTW, if the FDA "has a legitimate function in interstate commerce", what doesn't? The only legitimate functions of the federal government are expressly enumerated in the Constitution.
The Commerce Clause is an enumerated power listed in the United States Constitution (Article I, Section 8, Clause 3). The clause states that the United States Congress shall have power "To regulate Commerce with foreign Nations, and among the several States, and with the Indian Tribes". Courts and commentators have tended to discuss each of these three areas of commerce as a separate power granted to Congress. It is common to see the Commerce Clause referred to as "the Foreign Commerce Clause," "the Interstate Commerce Clause," and "the Indian Commerce Clause," each of which refers to a different application of the same single sentence in the Constitution.
Personally, I believe preventing toxic substances from being sold across state lines as "medicine" is a legitimate application of the commerce clause.
I don't have any desire for any 'scrips'
Most natural substances and supplements have little to no side effects and many of them work really well. In fact, better than the OTC and prescriptions that doctors recommend. So again, why am I going to rely on that system which I have seen fail over and over again? I prefer natural substitutes, which would be in higher demand if the manufactured crap wasn't being pushed onto doctors and onto the market by the FDA and their "know-it-all" scientists.
Towards the end of the period, a number of radioactive medicines, containing uranium or radium, were marketed. These apparently actually contained the ingredients promised, and there were a number of tragedies among their devotees. Most notoriously, steel heir Eben McBurney Byers was a supporter of the popular radium water Radithor, developed by the medical con artist William J. A. Bailey. Byers contracted fatal radium poisoning and had to have his jaw removed in an unsuccessful attempt to save him from bone cancer after drinking nearly 1400 bottles of Bailey's "radium water." Water irradiators were sold that promised to infuse water placed within them with radon, which was thought to be healthy at the time.
You don't really want to go back to the era of the medicine show do you? The FDA has a legitimate function in interstate commerce. It's just a simple question - is it being run for the benefit of the people of the benefit of the corporations?
Start running the FDA on legitimate science for the benefit of the people and you won't see interference with experimental drugs in terminal or extreme cases, but you will see cheaper drugs because of lower development costs. The FDA is now controlled by corporations that don't want to see a new, lower cost drug come in until their patent runs out so they keep the hurdle high and the new drugs out.
Right, because when I purchase things at the store, I always head to another state to purchase stuff there and then come back to the state I live in.
Well, I'm Hypo-thyroid and have serious asthma so I'd be dead without them. I f you want to rely on natural substances, fine, but don't take all the protection away from the drug market, some of us need them to live.
but don't take all the protection away from the drug market, some of us need them to live.
By the way, "radon" is a natural substance.
I, on the other hand, have hypothyroidism and have found it to be a wonderful cure (I was diagnosed a few years before I started smoking). Not only did the symptoms go away shortly after I started smoking daily, but I stopped taking the medicine I was prescribed and every blood test has shown my blood levels to be perfectly in range.
Apparently Canada has done some studies on the topic of hypothyroidism and cannabis.
Also there is quite a bit of anecdotal evidence:
http://forum.grasscity.com/6876223-post4.html
Amazing.
You thought you'd be dead without the FDA, turns out they just have you taking a bunch of chemicals instead of ingesting a plant.
I really dislike it when someone thinks their own "anecdotal experience" gives them the right to tell someone else what to do with their body.
Your "anectodotal evidence" is one isolated report, I found no "Canadian research" and the only research I found on cannabis and thyroid disease was with "HYPER-THYROIDISM".
The chemicals are hormone replacement - eating a plant would only work if it was hormone replacement. I have Hashimoto's, an inherited auto-immune thyroid disease. My thyroid gland is long gone.
And as for my asthma - I have scarred lung tissue.
I really dislike it when someone thinks their own "anecdotal experience" gives them the right to tell someone else what to do with their body.
Talk about a libertarian oxymoron......
Synthroid is the most prescribed brand of T4 in the United States. Synthroid was marketed in 1955, but was not FDA approved at that time as it was "generally regarded safe".[5] In the 1990s, in response to debate as to whether Synthroid was more effective than other levothyroxine preparations, (which ended up concluding that there was little difference between Synthroid and generic brands) all levothyroxine preparations were required to undergo the formal FDA approval process. Synthroid was approved by the FDA on 24 July 2002.[6]
Since virtually everyone falsely believes the FDA is protecting them, while it is really a genocidal agency.