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(visit the link for the full news article)
The Food and Drug Administration on Wednesday ordered the removal from the market of more than 500 prescription drugs used to treat colds, coughs and allergies because the medications had never gone through a federal review of their safety and effectiveness.
"We don't know what's in them, whether they work properly or how they are made," Deborah Autor, the director of the office of compliance in the FDA's drug division, said in a telephone news conference on Wednesday morning.
Originally posted by Vitchilo
FDA pulls more than 500 drugs off market
www.stltoday.com
(visit the link for the full news article)
The Food and Drug Administration on Wednesday ordered the removal from the market of more than 500 prescription drugs used to treat colds, coughs and allergies because the medications had never gone through a federal review of their safety and effectiveness.
"We don't know what's in them, whether they work properly or how they are made," Deborah Autor, the director of the office of compliance in the FDA's drug division, said in a telephone news conference on Wednesday morning.
Originally posted by HunkaHunka
reply to post by Vitchilo
Hrm... If you read the article you would know that there weren't any reports of death etc... That's the reason these slipped by for so long.
Why doesn't the FDA just pull all unapproved drugs off the market? "It's a resource-intensive process," so the agency must focus on potentially dangerous drugs, Autor says.
Do you realize how many doctors prescribe, pharmacists fill prescriptions for, and people take drugs that they have no idea are not FDA approved? Lots. These drugs are in the PDA and even appear online on many reference sites for both professionals and patients, and it's never mentioned that they are not FDA approved.
Originally posted by Maxmars
reply to post by ~Lucidity
Do you realize how many doctors prescribe, pharmacists fill prescriptions for, and people take drugs that they have no idea are not FDA approved? Lots. These drugs are in the PDA and even appear online on many reference sites for both professionals and patients, and it's never mentioned that they are not FDA approved.
Hmmm, the primary publishers of the reference used by physician's (as if the bible) and some patients does not deem it necessary to reflect the drug's status in the regulatory system? Sounds like the PDR is not a "reference" at all, but a marketing tool, to me. Which means physicians, whose ostensible raison d'etre is the health of their patients, should have demanded a reference listing which actually was a 'reference' tool; not a high priced encyclopedic advertising vehicle for Big Pharma.
But since the FDA is manned by politically appointed former and future Big Pharma employees, it kind of goes along with the whole travesty of for profit health care.
edit on 3-3-2011 by Maxmars because: (no reason given)
Originally posted by ~Lucidity
I was prescribed a sinus medication in 1999 (that just happens to be on this list). It was the first medication I had taken of any sort in 15 years. When I took the first pill, my skin literally crawled from head to toe for four hours, particularly the head, necessitating a trip to the ER. Six weeks later, all my hair fell out in one day. I know the drug is what did it.