Cox 2 Inhibitors

Cox 2 inhibitors were supposed to help millions of arthritis and pain sufferers but have led instead to bad side effects. Cox 2 drug side effects include heart attack and Stevens Johnson syndrome. Learn more about Vioxx, Bextra and Celebrex.

Cox 2 Inhibitors and NSAID Use & Serious Health Hazard Side Effects

Cox 2 Inhibitors are new drugs in the non-steroidal anti-inflammatory drug family, otherwise known as NSAIDs. NSAIDs include common over the counter drugs like ibuprofen and aspirin. Researchers have long been working on an NSAID that does not present side effects on the stomach and liver. Most NSAIDs are used to treat the conditions like arthritis, including rheumatoid arthritis, osteoarthritis and psoriatic arthritis, gout, dysmenorrheal, metastatic bone pain, headaches and migraine, postoperative pain, pain due to inflammation and tissue injury, pyrexia and renal colic.
 
COX 2 drugs have been specifically targeted (marketed) towards arthritis sufferers, specifically osteoarthritis and adult rheumatoid arthritis. They have also been popular for treating intense menstrual cramping. Unfortunately, Cox 2 inhibitors have been tied to heart problems. Many people who were prescribed these drugs then suffered major cardiovascular events like heart attacks, strokes and blood clots which led to serious injury and in some cases, death.
 
When Vioxx was aggressively launched to the market, it quickly became an amazingly popular medication. It was popular among both doctors and patients but in 2004 a study showed that people taking Vioxx doubled their risk of heart attack and stroke. Merck, the pharmaceutical giant behind Vioxx pulled the drug from the market and this action was followed by the release of more studies and evidence relating to Vioxx and heart problems. In fact, in a study released just after the Vioxx was pulled, out of 1.4 million patients of the Kaiser Permanente HMO, more than 27,000 sudden cardiac deaths were linked to Vioxx.
 
Bextra is another Cox 2 drug that has also been linked to heart attack and stroke as well as the fatal skin disease Stevens Johnson Syndrome (SJS). SJS is a powerful and bad reaction to drugs in most cases causing blisters and peeling skin. Pfizer did quickly add a black label warning about the potential of developing Stevens Johnson Syndrome as a result of taking the drug. After reports indicated that Bextra might be more dangerous than Vioxx, it too was pulled from the market.
 
Celebrex, marketed by Pfizer, remains on the market as the only COX II Inhibitor available. On March 1, 2006, a New Zealand based research group said that upon a re-analysis of older studies conducted on Pfizer's pain reliever Celebrex they have discovered that the drug can indeed raise the risk of suffering a heart attack. The drug, like other Cox 2 inhibitors Vioxx and Bextra can nearly double the risk of heart attack in patients.
 
The idea behind Cox 2 inhibitors was sound – isolate the anti-inflammatory benefits, among others, and try to eliminate problematic side effects that damage the stomach and renal systems. Sadly, because of inadequate testing and trials and a massively successful marketing campaign, thousands of people suffered painful injury and many people died. There are many lawsuits pending against Merck and Vioxx for the defective drugs they offered to the market. If you have been injured by Vioxx, Bextra or Celebrex you should contact a product liability, medical malpractice or defective drug attorney as soon as possible.

 

Informative Articles About COX-2 Inhibitors & Arthritis Medications

· Understanding the Risks and Alternative Uses of Cox-2 Inhibitors / Arthritis Medications

  4/18/2006 6:00:00 AM | Cox 2 Hazards and Alternative Arthritis Medications

· Vioxx Side Effects and Merck's Knowledge

  4/13/2006 9:15:00 AM | Vioxx Recall and Side Effects History

 Latest COX-2 / Arthritis & Related Newswire

· More Damaging Vioxx Evidence in Trial - San Jose Mercury News

  7/5/2006 9:30:00 PM | Witness says studies showed Vioxx users at risk of heart ailments
  Comments:(0)
   More compelling testimony for the plaintiffs in the California Vioxx trial: Dr. Lemuel Moye of the University of Texas said his analysis of early Vioxx trials concluded that the risks of heart attack and stroke outweighed the benefits.  Further, some trials excluded patients who were at a higher risk of heart attack, thus skewing the resu...
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· California Vioxx Trial Hears More Testimony About Clinical Studies - North County Times

  6/30/2006 3:12:00 PM | Merck Scientist Testifies Vioxx Caused More Heart Attacks Than ...
  Comments:(0)
   Jurors for the California Vioxx trial continued to view videotaped depositions on the third day of the trial. A Merck researcher, Dr. Deborah Shapiro, testified that a 1999 study of 8000 patients showed that those given Vioxx had four times the number of heart attacks than those given Aleve (naproxen), an older NSAID. Merck claims that there i...
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· Testimony Begins in California Vioxx Trial: Merck Did Not Submit Test Results to FDA - San Jose Mercury News

  6/29/2006 3:04:00 AM | Testimony: Feds not told about tests that exposed Vioxx dangers
  Comments:(0)
   The former head of Merck's research laboratories was heard in a video deposition on the second day of the Vioxx trial in California. Dr. Edward Scolnick said that two studies in 2001 showed that patients on Vioxx were 2-4 times more likely to die than patients on placebo; however Merck did not submit these results to the FDA. Merck is being su...
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· Opening Statements in California Vioxx Trial - NorthJersey.com

  6/28/2006 9:13:00 AM | Plaintiff says Merck knew of potential dangers with Vioxx
  Comments:(0)
   The first Vioxx trial to be held in California is under way.  In opening statements, the plaintiff's lawyer said that Merck was aware of Vioxx's risks as far back as 1996 and did not inform doctors. Furthermore, the company specifically trained salespeople to downplay the risks. Stewart Grossberg claims the drug caused his heart attack an...
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· Vioxx Study Retraction Issued by New England Journal of Medicine - Lex 18

  6/27/2006 10:11:00 PM | Journal Corrects Vioxx Article to Reflect Short-Term Heart Risk
  Comments:(0)
   The New England Journal of Medicine has issued a correction with regard to a study on the heart risks of Vioxx. The study, released in 2005 and funded by Merck, the drug company that made Vioxx, concluded that the risks of heart attack began only after 18 months of Vioxx treatment.  A followup study, however, adds more data which suggests...
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Comment On: Testimony Begins in California Vioxx Trial: Merck Did Not Submit Test Results to FDA
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Comment On: Vioxx Side Effects and Merck's Knowledge
Posted by Thomas1 on 10/5/2007 | Filed Under: Vioxx (Rofecoxib)

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Comment On: Testimony Begins in California Vioxx Trial: Merck Did Not Submit Test Results to FDA
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