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celebrex lawsuits Nnually. About 27 million patients have been prescribed Celebrex in the United States alone. Celebrex was approved by the FDA in 1999 to treat the acute pain associated with osteoarthritis celebrex lawsuits, rheumatoid arthritis celebrex lawsuits, and primary dysmenorrhea. Concerns over the safety of Celebrex were raised almost immediately after this drug was approved for use in the United States. After three months of availability celebrex lawsuits, The Wall Street Journal published an article about ten deaths that had been linked to Celebrex use. Gastrointestinal hemorrhage was the cause of half of these deaths. Other causes of death included heart attack celebrex lawsuits, kidney problems celebrex lawsuits, and drug interaction. Celebrex use w celebrex lawsuits.

celebrex lawsuits As never officially deemed responsible for these deaths though each of these patients had been taking Celebrex at the time of death. This report may prove to be a haunting foreshadowing of recent clinical studies that are indicating fatal side effects associated with Celebrex use. On December 17 celebrex lawsuits, 2004 Pfizer publicly announced that patients who are taking Celebrex may have an elevated risk of suffering heart attack and stroke. The National Cancer Institute designed a study to research the effects of Celebrex on cancer. This Pfizer-sponsored study was suspended after preliminary evidence showed that clinical trial patients who were taking 400 to 800 milligrams of Celebrex were two and a half times more likely to suffer from heart attack or cardiovascular stroke than patients in the control group. These findings come just two months after the recall of a medication quite similar to Celebrex in form and function. Vioxx was voluntarily pulled off the market by Merck pharmaceuticals celebrex lawsuits, after internal clinical studies revealed that patients who had taken Vioxx for eighteen months were twice as likely to suffer from stroke or heart attack as the general population. Since the Vioxx recall on September 30 celebrex lawsuits, 2004 celebrex lawsuits, Merck has been subject to thousands of Vioxx lawsuits. If the preliminary evidence regarding Celebrex cardiovasc.

celebrex lawsuits of Celebrex were two and a half times more likely to suffer from heart attack or cardiovascular stroke than patients in the control group. These findings come just two months after the recall of a medication quite similar to Celebrex in form and function. Vioxx was voluntarily pulled off the market by Merck pharmaceuticals celebrex lawsuits, after internal clinical studies revealed that patients who had taken Vioxx for eighteen months were twice as likely to suffer from stroke or heart attack as the general population. Since the Vioxx recall on September 30 celebrex lawsuits, 2004 celebrex lawsuits, Merck has been subject to thousands of Vioxx lawsuits. If the preliminary evidence regarding Celebrex cardiovascu.

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Proxen and other appropriate drugs. Why Did the FDA Allow Celebrex to Stay on the Market? Although Celebrex® has been linked to an increased risk of heart attack and stroke, the available research does not support a conclusion that the risk associated with Celebrex® is significantly greater than the risk associated with the other non-selective NSAIDs, except aspirin. To counter the risk, the FDA required the manufacturers of NSAIDs, including Celebrex®, to revise their labeling to include a "boxed" or serious warning highlighting the potential increased risks of cardiovascular events, as well as the risk of stomach bleeding. Celebrex® must also include a specific warning against patients taking the drug either right before or right after heart surgery. What Risks are Associated with Taking Celebrex? Like Vioxx® and Bextra®, Celebrex® has been linked to an increased risk of heart attacks or strokes in patients who have taken the drug for long periods of time. Patients taking Celebrex® have suffered bleeding ulcers, liver damage, kidney problems leading to kidney failure, and fluid retention. Why is Pfizer Being Sued?Both Merck and Pfizer spent hundreds of millions of dollars advertising their "miracle" pain relievers, especially Vioxx® and Celebrex®, directly to the public. Some argue that the aggressive ad campaigns created a false image of the drugs being absolutely safe. With both Vioxx® and Bextra® being pulled from the market because of the link to heart attacks and strokes and Celebrex® being linked to same cardiovascular risks, Celebrex® users question whether Pfizer

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