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Adderall — prescribed to treat narcolepsy and "attention deficit hyperactivity disorder" (ADHD) in children as young as two — are in fact no different in action from meth. ... In fact, the active ingredients of Adderall are actually 75 percent dextroamphetamine salts; the other 25 percent are other amphetamines.
originally posted by: schuyler
Methamphetamine and dextroamphetamine are chemically different, though obviously related. But the fact is methamphetamine is available as a prescription itself. It's called Desoxyn. Under controlled conditions for certain disorders, either can be helpful. But that doesn't mean "therefore crystal meth" is okay.
If you believe it is, take a look here.. The people in these pictures "voted with their dollars" just like you advocate.
originally posted by: Cobaltic1978
originally posted by: schuyler
Methamphetamine and dextroamphetamine are chemically different, though obviously related. But the fact is methamphetamine is available as a prescription itself. It's called Desoxyn. Under controlled conditions for certain disorders, either can be helpful. But that doesn't mean "therefore crystal meth" is okay.
If you believe it is, take a look here.. The people in these pictures "voted with their dollars" just like you advocate.
Yeah, I would never had guessed you are only 29.
originally posted by: Cobaltic1978
Naturalnews is a source that is frowned upon here. In fact, I think it's thought of worse than that, maybe even banned from here.
originally posted by: schuyler
Methamphetamine and dextroamphetamine are chemically different, though obviously related. But the fact is methamphetamine is available as a prescription itself. It's called Desoxyn.
originally posted by: Nyiah
originally posted by: schuyler
Methamphetamine and dextroamphetamine are chemically different, though obviously related. But the fact is methamphetamine is available as a prescription itself. It's called Desoxyn.
^^ This. It's legally sold as Desoxyn, not Aderall.
Also, remember this blatant line of BS next time you take NN at it's word.
originally posted by: mOjOm
a reply to: schuyler
I was talking to this old timer I know I while back that was telling about how when he was younger he new people that had a script for meth from their doctor. The would give it to people for a variety of things like weight loss and some other stuff.
I never realized it was once considered a legit drug by doctors. That makes me wonder what drugs today are going to be tomorrows outlaw drug
All food and drugs should be regulated only by consumers in the marketplace by voting with their dollars about what is safe and what isn't, which companies are ethical and which are not, and which treat their employees well enough and which don't.
originally posted by: theantediluvian
All joking aside, the FDA wasn't created for no reason. We're talking about people drinking radioactive water, using cosmetics that left them blind, children dying from contaminated medicines and even a few mass casualty incidents. So yeah, the FDA isn't perfect but the state of affairs prior to its creation was worse.
Thalidomide first entered the German market in 1957 as an over-the-counter remedy, based on the maker’s safety claims. They advertised their product as “completely safe” for everyone, including mother and child, “even during pregnancy,” as its developers “could not find a dose high enough to kill a rat.” By 1960, thalidomide was marketed in 46 countries, with sales nearly matching those of aspirin.
Around this time, Australian obstetrician Dr. William McBride discovered that the drug also alleviated morning sickness. He started recommending this off-label use of the drug to his pregnant patients, setting a worldwide trend. Prescribing drugs for off-label purposes, or purposes other than those for which the drug was approved, is still a common practice in many countries today, including the U.S. In many cases, these off-label prescriptions are very effective, such as prescribing depression medication to treat chronic pain.
However, this practice can also lead to a more prevalent occurrence of unanticipated, and often serious, adverse drug reactions. In 1961, McBride began to associate this so-called harmless compound with severe birth defects in the babies he delivered. The drug interfered with the babies' normal development, causing many of them to be born with phocomelia, resulting in shortened, absent, or flipper-like limbs. A German newspaper soon reported 161 babies were adversely affected by thalidomide, leading the makers of the drug—who had ignored reports of the birth defects associated with the it—to finally stop distribution within Germany. Other countries followed suit and, by March of 1962, the drug was banned in most countries where it was previously sold.
In July of 1962, president John F. Kennedy and the American press began praising their heroine, FDA inspector Frances Kelsey, who prevented the drug’s approval within the United States despite pressure from the pharmaceutical company and FDA supervisors. Kelsey felt the application for thalidomide contained incomplete and insufficient data on its safety and effectiveness. Among her concerns was the lack of data indicating whether the drug could cross the placenta, which provides nourishment to a developing fetus.