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Originally posted by Vajrayana
Thanks for the Nexia update soficrow,they really are like a real modern day Dr. Moreau.I think the military will stop at nothing to get their VX antidote,even with the present absence of an impending chemical attack.My main concern would be these transgenic goats being potentially mishandled by mix-up,escaping, or accidentally introduced into the normal goat population,forever contaminating the species with its genetic mutations and the repercussions it could lead to regarding the health-risks of consumers of their milk & cheese.
Also the clinical development program being regulated under the FDA's Animal Efficacy Rule.If we can't trust them to alert fellow humans to potential dangers of drugs,we certainly can't expect them to institute proper regulation or monitoring of animals.
Protexia's risks go beyond the now normal dangers of untested drugs - and into the realm of biotech - IMO, just as bad as the goat thing. ....And all this is happening without any monitoring or oversight.
Originally posted by Vajrayana
biotech definitely has been tinkering with pandora's box - getting bolder by the day....A few years ago I attended a lecture given by Daniel Botstein about the future of genomics.A lot of the discussion was centered around pathogenicity,encoded transcriptase/reverse transcriptase,pria,archea,cancer,marburg & ebola viruses,etc. but some of the methods being proposed & discussed certainly required an ethics-free approach.
I'm always on the lookout for identifying any poison-the-many to cure-the-chosen-few supporters and they certainly can be found lurking in the publish-hungry grant-driven realm of biotech.
Cox-2 drugs may suppress immune function
Analgesics called Cox-2 inhibitors, which U.S. health officials restricted Thursday, can not only damage the heart and blood vessels but may also suppress the immune system, researchers said.
A study published this week in the Journal of Immunology shows the drugs, used by arthritis sufferers, might affect the antibodies that attack invading germs. ...This could be both good news and bad news for the drugs, which have also recently been shown to double or triple the risk of heart attacks and strokes, the researchers at the University of Rochester in New York said. ...Pfizer Inc. suspended sales of its Cox-2 inhibitor Bextra Thursday at the request of U.S., European and Canadian regulators.
The Food and Drug Administration also asked Pfizer to include a strong “black box” warning for its Cox-2 drug Celebrex. Merck & Co.’s Cox-2 Vioxx was withdrawn last year.
Also see: Painkiller Bextra pulled from market
Originally posted by jholden
Although you make a connection between Vioxx and the accelerated progression of FMD, there is no evidence in your article or direct statements that Vioxx can CAUSE the disease.
This would mean that the Vioxx only affects those who already have FMD, and merely makes it worse.
One might conclude then, that Vioxx is safe for those who do not already have FMD.
Are there direct links of Vioxx as a CAUSE of FMD? Do you know of any sources which imply that there is a CAUSAL relationship?
Adiponectin: Healing a wounded heart OR
Adiponectin
Adiponectin stimulates AMP-activated protein kinase (AMPK) and COX-2 to prevent myocyte apoptosis and reduce inflammation after ischemic heart injury.
Original research papers: Nature Medicine 11, 1096 - 1103 (2005)
(One or the other of these links should work - but you probably will need to sign up for a free subscription.)
Merck One; Plaintiffs One
After deliberating for less than eight hours over three days, the jury cleared Merck of allegations it failed to warn consumers about the drug’s risks and engaged in “unconscionable commercial practices” in marketing it to doctors and their patients.
The verdict was Merck’s first win out of two Vioxx-related trials. In August, a Texas jury found the company liable in a Vioxx user’s death.
Only one juror, casino worker Juan Garcia, voted that Merck failed to give adequate warnings to doctors about the link between Vioxx and increased risk of heart attacks and strokes. ...“I think they should have known and explained more to the doctors and everyone,” Garcia said. He said he also believed Vioxx was a factor in causing Humeston’s heart attack.
But Vickie Heintz, who works in a manufacturer’s credit department, said she believed stress and Humeston’s other health problems were responsible for his heart attack. ...“I thought he had way too many health other issues,” Heintz said. “His medical records were riddled with many medicines.”
Journal: Merck hid bad Vioxx outcomes
Vioxx maker Merck & Co. concealed heart attacks suffered by three patients during a clinical study of the now-withdrawn painkiller in a report on the study published in the New England Journal of Medicine in 2000, the journal wrote in an editorial released Thursday.
The editorial, written by the journal’s editor in chief, Dr. Jeffrey M. Drazen, executive editor Dr. Gregory D. Curfman and a third doctor, also alleges the study’s authors deleted other relevant data before submitting their article for publication. ...“Taken together, these inaccuracies and deletions call into question the integrity of the data on adverse cardiovascular events in this article,” the doctors wrote. ...Adverse cardiovascular events include heart attacks, strokes and deaths.
One of the study’s authors was Dr. Alise Reicin, Merck’s vice president for clinical research. Reicin on Wednesday testified in the Houston trial that the company never misled doctors and the public about studies linking heart attacks to Vioxx.
The company now faces at least 7,000 lawsuits over Vioxx and legal liability some analysts have estimated at up to $50 billion. Those problems were part of the reason Merck last week announced plans to cut 7,000 jobs and close eight manufacturing and research facilities around the world as the first step in a sweeping reorganization.
The journal editors also again criticized Merck and the study's outside co-authors for failing to report the total number of serious thromboembolic events — including heart attacks, strokes and blood clots — among patients taking Vioxx in the trial. An internal Merck memo revealed that 47 patients on Vioxx suffered those problems, compared with 20 taking naproxen, according to the editors.
A jury on Wednesday found Merck & Co. failed to warn Vioxx users of the drug's heart risks and ordered it to pay a 77-year-old plaintiff at least $4.5 million in a decision that raises questions about the company's future defense of thousands of lawsuits filed over the medicine.
The jury determined that the company knew or should have known that its pain drug increased the risk of heart attacks and other cardiovascular events, but didn't adequately warn users or their doctors.
Wow Marge do we have the same Dr?,I took all the above,can also throw in Paxil CR,though neurotrin drove me 5150,I'm no worse for wear and tear
Originally posted by marg6043
I took all of them vioxx, naprozen, bextra, and all the above, during the 90s and all the way to 2004, I never got a hart attack, but I did end up in the hospital from a "panic attack" I got over it, with not medications.
I used to love bextra I was taken 20 mg two times a day and so vioxx.
I was also on neurontin and that is on the review also.
I guess I should complain about my "panic attack" and get my name on the list for some money.