Guest guest Posted August 4, 2005 Report Share Posted August 4, 2005 I know there is great interest here in doing studies to validate the use of LDN as a viable medical treatment. Working with clinical trials and the sometimes questionable results surrounding cancer research, I still pose the question as to the logic of that decision. The following is a portion of an article from MSNBC.com dealing with the mis-truths and sometimes just plain fabrications that occur regularly in the medical community concerning drugs, procedures, etc... I am not inferring that this would happen, but I think it is a viable question to consider. More importantly, one study does not a solution make. From a statistical standpoint, a single study is a novelty. It has little more validity than a single good result of an individual inside of a study group. This is why clinical trials consist of multiple studies before they are allowed to make claims of any kind. Please just keep these things in mind. I do not want to see people hurt from either side of this if the results come back good or bad. MSNBC.com WHAT'S GOOD FOR YOU OFTEN ENDS UP BEING BAD Nearly one-third of initial medical studies misleading, major review finds CHICAGO - Here's some medical news you can trust: A new study confirms that what doctors once said was good for you often turns out to be bad or at least not as great as initially thought. The report is a review of major studies published in three influential medical journals between 1990 and 2003, including 45 highly publicized studies that initially claimed a drug or other treatment worked. Subsequent research contradicted results of seven studies, ?16 percent,? and reported weaker results for seven others, an additional 16 percent. That means nearly one-third of the original results did not hold up, according to the study in Wednesday's Journal of the American Medical Association. Contradicted and potentially exaggerated findings are not uncommon in the most visible and most influential original clinical research, said study author Dr. Ioannidis, a researcher at the University of Ioannina in Greece. [[[[NOTE: Look at all the drugs marketed and subsequently taken off the market as clearly dangerous and deadly. Within the short space of 9 months, 3 FDA-approved drugs have had to be removed from the market due to lethal side effects, that became known, not during pre-marketing safety and efficacy trials, but very soon into their post-marketing, prescription use. Both Duract, a non-steroidal anti-inflammatory pain pill, and Redux dexfenfluramine of Fen-Phen fame, a weight loss agent are manufactured by Wyeth Ayerst. Duract was recalled due to 12 cases of liver failure while Redux (alone and in combination with phentermine: Fen-Phen) was found to cause serious heart valve deformities. Posicor, the third, an antihypertensive marketed by Roche Laboratories, has proved lethal upon interacting with an array of widely prescribed medications. Only three times in the past decade has the FDA removed previously approved drugs due to adverse post clinical trials, post-marketing experience. However, as pointed out by journalist Kuttner [The American Prospect, 6/29/98]. The FDA's approval of drugs that later turned out to have lethal side effects is the predictable result of an industry campaign, abetted by Congressional Republicans, to speed up the approval process. This is part of a larger pattern in which the health and safety of the public are being sacrificed to the profit motive? These needless deaths an injuries are a result of this drug-approval stampeded. There is no such thing, prior to marketing (pre-marketing) as a long-term study and yet the FDA provides for no formal, publicly available survey of postmarketing experience. That this is so is clearly to protect industry economic interests, regardless of the risk to the public.]]] ONE STUDY IS NOT ENOUGH Experts say the study is a reminder to doctors and patients that they should not put too much stock in a single study and understand that treatments often become obsolete with medical advances. A single study is not the final word, and that is an important message, editors at the New England Journal of Medicine said in a statement about the study. [[[How many of these faulty 'positive' studies were pharma sponsored, i.e., published due to pharma pressure, or financial influence--number of drug ads carried in that particular journal. The through-and-through rottenness is evident]]] The refuted studies dealt with a wide range of drugs and treatments. NOTHING'S BLACK AND WHITE Ioannidis study examined research in the New England Journal of Medicine, Lancet and JAMA prominent journals whose weekly studies help feed a growing public appetite for medical news. [[[Note: One thing that is black and white is that years of publications about psychiatric " chemical imbalances " of the brain in JAMA and all of the leading journals of the world have represented them to be real, actual, diseases, spearheading the deception of the public at large for the sole purpose of marketing, selling " chemical balancers " --psychiatric drugs. None, so far, have admitted this. Mr. Tom Cruise debunked " chemical imbalances " on the 6/24/05 Today Show and this was verified by Dr. ph Glenmullen on the 6/27/05 Today Show. I sent a letter to the President of the AMA, charging they collude in the fraudulent " chemical imbalance " representation. ]]] [To read the full article, please click link below.] ? 2005 MSNBC.com URL: _http://www.msnbc.msn.com/id/8554829/_ (http://www.msnbc.msn.com/id/8554829/) Bruce Guilmette, Ph.D. Survive Cancer Foundation, Inc. http://www.survivecancer.net Quote Link to comment Share on other sites More sharing options...
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