Prozac over the counter substitute for methadone. There was one problem: In order to do that, the FDA required that methadone's side effects be limited to the nausea it caused, with no mention of depression or any other psychiatric side effects.
And that was in 1994. By 1999, just a few years after Methadone was finally approved for prescribing over-the-counter to millions of people, the same thing happened. By then, it was known that methadone not effective in treating opiate addiction, and the FDA did not want to take sides in an issue that was causing problems. The new FDA policy of not testing methadone for depression was a slap in the face to millions of addicts who trusted the drug.
So, rather than allowing consumers to find the drugs that were best for them via research and their own experience, the FDA decided it would allow doctors to make treatment decisions.
The new policy was made permanent in 2010 when a Federal district court judge ruled that the government was not exempt from the FDA's oversight of medical medications. That left those who had developed a problem or were concerned about their mental health as out in the cold.
According to Dr. Gary Stevens, chief clinical officer of the Opioid Alternative and Research Alliance (Oarius) of Chicago: "The decision the FDA and Department of Justice is based upon the fact that you can't prevent people from getting drugs that are going to solve a problem … and then give a green light to the people who are creating problem."
Stevens says that a drug like the OxyContin, used to get high and which causes many of the same symptoms as heroin, is an example of the way pharmaceutical companies are being given a free pass for the same problem. (Stevens is a former medical director in the Department of Veterans Affairs.) He says pharmaceutical companies won't release a drug with potential side effect until it has been on the market for more than a year.
The law has allowed many other issues that have plagued U.S. medicine to not get as much attention addiction. It has also given pharmaceutical companies and doctors a free pass when it comes to the drug EpiPen, which can save lives by injecting an automatic response for anaphylactic shock into a potentially allergic person before all other action may be needed.
But it hasn't gone unrecognized by some doctors, including one who specializes in addiction medicine.
Dr. Robert Hinshot worked at a medical clinic in Pennsylvania specializing addiction issues for years. He was well known and trusted among doctors. Then, in 2011, Dr. Richard A. Friedman and several doctors sued the federal government in an attempt to have the government reclassify EpiPen, which is used to treat anaphylactic shock, so it would be easier for people to get.
Because the lawsuit was a class action, it consolidated in federal court Philadelphia with several other class actions filed against the federal government over same issues. That legal fight has had little impact and is scheduled to conclude with a resolution sometime in April of next year.
At this point, Dr. Hinshot does not expect his lawsuit and class action to change generic drugs canada pharmacy the regulations, citing FDA's rules that it has to wait for approval before changing a drug to make it more effective or safer than it was in is lorazepam generic for ativan 1994. "The people getting addicted have become an afterthought from the perspective of how important it is to continue push the drug and keep people off other drugs," he says. "They haven't"
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