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Bextra FAQs

What is Bextra used for?
Bextra (valdecoxib) is in a class of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Valdecoxib works by reducing substances in the body that cause inflammation, pain, and fever, and is used to reduce pain, inflammation, and stiffness caused by osteoarthritis and adult rheumatoid arthritis. Valdecoxib is also used to treat painful menstruation.

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Who should not take Bextra?

You should not take Bextra if you:

had asthma, hives or allergic reactions after taking aspirin or other NSAIDs (nonsteroidal anti-inflammatory drugs) or COX-2 inhibitors. Some examples of NSAIDs are ibuprofen (Motrin, Advil), naproxen (Naprosyn, Aleve), diclofenac (Voltaren, Cataflam), nabumetone (Relafen), ketoprofen (Orudis), celecoxib (Celebrex), and rofecoxib (Vioxx). You can ask your doctor or pharmacist for a complete list of these medications are allergic to valdecoxib (Bextra) or to any of the ingredients in Bextra.

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What should I tell my health care provider?

Tell your health care provider if you:

  • have heart problems or high blood pressure
  • have liver or kidney problems
  • have or had stomach ulcers or stomach bleeding
  • have asthma
  • are allergic to aspirin or other NSAID medicines
  • are pregnant or planning to become pregnant
  • are breast-feeding

Tell your health care provider about all the medicines that you are taking, including prescription and non-prescription medicines, vitamins, and herbal supplements. Your health care provider may have to adjust your dose or watch you more closely if you take the following medications:

  • certain blood pressure medicines called ACE inhibitors
  • furosemide (Lasix)
  • fluconazole or ketoconazole
  • lithium
  • warfarin (coumadin)
  • aspirin

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What are some possible side effects of Bextra?

Some of the more serious, possible side effects of Bextra include:

  • Abdominal pain, tenderness, or discomfort
  • Bloody, black, or tarry stools
  • Bloody vomit
  • Unusual fatigue or lethargy
  • Yellowing of the skin or eyes
  • Unusual bruising or bleeding

Pfizer also said it is updating its label on Bextra to strengthen a warning about a rare but serious skin reaction, Stevens-Johnson syndrome, that can occur mainly within the first two weeks of therapy.

Less serious, but sometimes life threatening side effects can include:

  • Indigestion
  • Nausea
  • Stomach pain
  • Upper respiratory tract infection
  • Diarrhea
  • Headache
  • Rarely serious ulcers and stomach bleeding have occurred in patients taking Bextra.

If you are experiencing any of the above listed side effects, and have taken Bextra, contact Belluck & Fox immediately for a free legal evaluation. Drug litigation can be extremely complex. It is best to seek the counsel of a personal injury attorney with experience in this field of law. Belluck & Fox has substantial experience with defective product litigation, including pharmaceutical and medical product cases. We will provide you with personalized, professional legal representation.

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How can an arthritis drug lead to heart attack and stroke?
Scientists say they are not sure. However, several studies have indicated that Bextra, Vioxx, Celebrex, and other COX-2 inhibitors are known to raise blood pressure and increase the risk of heart attack. Drugs such as Vioxx and Pfizer's Bextra & Celebrex inhibit Cox-2, an enzyme that triggers pain and inflammation.

Pfizer also said it is updating its label on Bextra to strengthen a warning about a rare but serious skin reaction, Stevens-Johnson syndrome, that can occur mainly within the first two weeks of therapy.

Vioxx has also been associated with several other life-threatening side effects, including blood clots, angina and nonbacterial meningitis, severe intestinal damage, ulcerations and bleeding, and kidney damage.

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What can I take instead of Bextra?
Older medications like ibuprofen, naproxen or simply aspirin have been used as alternatives for Bextra, Vioxx and Celebrex.

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What should I do if I am currently taking Bextra?
Contact your doctor to discuss discontinuing use of Bextra and possible alternative medications. If you have experienced any side effects, contact a lawyer to review your case. We understand your medical concerns take priority, but don't ignore your legal right to compensation.

Your state's law may limit your time to bring a legal claim. To protect your rights, you need to have your personal injury claim evaluated immediately.

Free Bextra Case Evaluation

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What should I do if I have been a victim of prescription drugs / pharmaceutical negligence?
You may be experiencing pain and suffering and severe financial hardships. You should not go through this difficult time alone. You, the patient, should not be paying for your doctor's mistakes or negligence.

If you or a loved one are living with the consequences of the effects from Bextra, it is important to contact an experienced lawyer who can protect your rights and get you the compensation to which you are entitled.

Our Bextra Lawyers have a track record of success representing your rights against drug manufacturers. We are available to discuss your potential claim, and answer any questions you might have. Call us for a Free Case Evaluation : 1.877.LEGAL03

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Related VIOXX FAQs from VIOXX LAWYERS

What is Vioxx?

Vioxx is a popular anti-inflammatory medication introduced to the U.S. market in 1999, and used to be prescribed to ease the pain, swelling and other symptoms of osteoarthritis. Before drug maker Merck & Co. withdrew it from the worldwide market September 30, 2004, it was most commonly given to patients with Osteoarthritis. Vioxx belongs to a class of medications known as cyclooxygenase-2, or COX-2, inhibitors. Sales topped $2.55 billion in 2003.

Vioxx – a non-steroidal, anti-inflammatory drug (NSAID) – is in a class of drugs commonly referred to as "Cox-2 Inhibitors". It comes in liquid or pill form, and is prescribed to relieve the symptoms of osteoarthritis. It can also be used to treat acute pain in adults such as those patients who experience severe pain associated with menstruation. Vioxx works by blocking COX-2 enzymes in the body that trigger pain and inflammation.

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Why did Merck take Vioxx off the market?
Merck pulled its best-selling arthritis drug off the market based on data indicating the drug increases the risk of heart attack and stroke among users.

Merck announced the immediate, voluntary worldwide withdrawal after a three-year colon cancer clinical trial with 2,600 patients revealed that 18 months after patients started taking Vioxx, test results showed an increased risk of heart attacks and other cardiovascular complications.

84 million people have used Vioxx since 1999.

In previous years, Merck consistently denied any possible links between Vioxx and cardiovascular problems.

The drug was licensed in June 1999. Since then, more than 20 million Americans have taken the drug at one time or another. In September 2001, the FDA sent Merck an eight-page warning letter about the company’s promotional campaign for Vioxx. The letter indicated that the campaign minimized “the potentially serious cardiovascular findings that were observed” in a trial that compared the drug to naproxen, a less-expensive painkiller. The FDA charged that Merck discounted the fact that "patients on Vioxx were observed to have a four to five-fold increase" in heart attacks, compared with patients on naproxen.

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How can an arthritis drug lead to heart attack and stroke?

Scientists say they are not sure. However, several studies have indicated that Vioxx and other COX-2 inhibitors are known to raise blood pressure and increase the risk of heart attack. Drugs such as Vioxx and Pfizer's Celebrex inhibit Cox-2, an enzyme that triggers pain and inflammation.

Vioxx has also been associated with several other life-threatening side effects, including blood clots, angina and nonbacterial meningitis, severe intestinal damage, ulcerations and bleeding, and kidney damage.

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What are the side effects of Vioxx?
Vioxx side effects may include, but are not limited to, heartburn, nausea, diarrhea, upper respiratory tract infection, swelling of the lower extremities (legs and/or feet), high blood pressure, itching, stomach ulcers or bleeding, fatigue, vomiting, dark urine, and black stools.

In addition to increasing risk of heart attack and stroke, patients taking Vioxx were found to be four times more likely to suffer from heart attack than those taking Naproxen (Aleve). Vioxx is more likely to cause severe intestinal damage, ulcerations and bleeding, blood clots and toxic epidermal necrolysis (a fatal skin disease), than other arthritis pain relievers.

Other health problems include:

  • Serious kidney problems that could lead to acute kidney failure.
  • Serious liver problems.
  • Allergic reactions, such as swelling of the face, lips, tongue, and throat which can cause difficulty breathing or swallowing.
  • The FDA reports that Vioxx has also been linked to at least five cases of a non-bacterial type of meningitis, a rare but serious side effect.

These conditions may come about suddenly with few or no symptoms. If left untreated, hospitalization or even death can occur.

If you, or a loved one, have taken Vioxx and experienced any side effects, contact our pharmaceutical negligence lawyers today, for a free evaluation - 1.877.LEGAL03

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What does this mean for Celebrex or Bextra, the other two drugs in the class known as COX-2 inhibitors?

In light of the Vioxx study findings, several top scientists have stated that the finding of an elevated risk of heart attacks and strokes applies to all COX-2 inhibitors. Clinical trials of Celebrex and Bextra did not reveal the same problems as Vioxx because participants were allowed to take aspirin, which has proved to reduce the risk of cardiovascular problems.

Pfizer, maker of Celebrex and the less-prescribed Bextra, stands by its products. But studies are continuing to review the link of these drugs to cardiac problems.

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Phone: 212-681-1575
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