Purdue Pharmaceuticals about to make oxycontin look like a day at the beach?, page 1
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reply posted on 5-1-2005 @ 09:40 PM by Bleys
Originally posted by TKainZero
i was googleing to try to find more info on this and i cant can you post a link?


I found this
Press Release :

Stamford, Conn., September 24, 2004 – The U.S. Food and Drug Administration (FDA) has approved Palladone™ (hydromorphone HCl extended-release) Capsules (CII) for the management of persistent, moderate to severe pain in patients requiring continuous, around-the-clock analgesia with a high potency opioid for an extended period of time (weeks to months) or longer. The painful conditions may arise from either cancer or non-cancer conditions. While long-acting (q12h) hydromorphone formulations are available in Canada, the United Kingdom, and Germany, Palladone is the first long-acting hydromorphone formulation available in the U.S. The product offers the convenience of once-daily (q24h) dosing and will be available in 12 mg, 16 mg, 24 mg, and 32 mg dosage strengths. Palladone Capsules are expected to be available in retail pharmacies in the first half of 2005.


Purdue Pharmaceuticals website can be found - here

B.


reply posted on 7-1-2005 @ 03:54 PM by justme1640
FLYIN HIGH I know just what you mean -- isn't it frustrating when people who don't have chronic pain think we get high on pain meds -- Like you say we take them just to function somewhat normally. I didn't take what you take -- I took Darvocet - I usually managed to keep it to 2 pills mid-day just to be able to get the pain level to come down a few notches for a few hours. I was so careful not to overdue what I took. (if I had 60 for the month I might not take any if the day wasn't horrendous but then on a day where it was I might take one before going to bed to be able to hopefully fall asleep) Now with the government scaring doctors -- trying to get needed pain meds you are made to feel like an addict. I had one great doctor who understood and said that I would never be addicted but I was dependent on them to function. Of course that doctor went to boutique medicine and I couldn't afford the $1,500 fee a year to be his patient. So now I go to an urgent care doctor as most doctors in this area aren't taking new patients. I am miserable- I am in pain- I don't sleep - which causes the pain to be worse which causes me to not sleep ---- a never ending cycle it seems. Because my activity level has decreased and because I am eating because I hurt and am ticked off about it my weight has gone up. BTW the doctor I go to now will give me pain meds but I don't want to put him in the position of defending his belief that people need relief. I now am destroying my stomach with Advil, Aleve, or asprin which really have no effect at all on how I feel. Every few months I can't take it and do get a months script and am amazed at how much better I feel with just the 2 pills a day -- I am still in pain but I have a few hours of it being a level 6 instead of a level 8 or 9.

You can tell that people who get up in arms about pain meds have never had chronic pain. I do agree that there is a concern that it will be used illegally and abused by some -- but honestly that is not my problem. That is up to the doctors to decide if their patient needs the meds or not. And as far as what will get on the street illegally -- it isn't my fault ----I shouldn't have to pay for it with more pain.

There was an article in AARP magazine this month that quoted a study done at Northwestern Feinberg School of Medicine (the article was in the Nov. 17th issue of Journal of Neuroscience) that stated that chronic unrelenting pain (their particular study was done on back pain) causes the brain's gray matter to shrink as much as 11% in one year - that is the equivalent of 10-20 years of aging. And that the area that loses the gray matter are areas that process information and memory.

Sorry to go off on everyone -- but this is a sore point with me -- pun intended.
jm
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