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Fosamax Injury Attorney
Fosamax, also known as alendronate, is a medication used for bone loss, but has been implicated in the serious necrosis of the jaw and other bones, a condition known as "osteonecrosis" (ONJ) – also called "bone death." Click here for more information regarding Fosamax lawsuit

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Bextra Injury Lawyer
The FDA required all NSAIDs (prescription and non-prescription alike) to include a black-box warning – the most serious – on all future packaging, highlighting "the potential for increased risk of cardiovascular events and the well described, serious, potential life-threatening gastrointestinal bleeding associated with their use." Click here for more information regarding Bextra lawsuit

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ReNu MoistureLoc Lawsuit
ReNu with MoistureLoc was permanently pulled from shelves worldwide on May 15 after Bausch & Lomb admitted an issue with their formulation and relation to fusarium. The FDA reports “A fungus called Fusarium has been identified as the cause of the reported infections. As of April 9, 2006, 109 cases of suspected Fusarium keratitis are under investigation by CDC and public health authorities in 17 states of the U.S. Click here for more information regarding ReNu MoistureLoc lawsuit

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Children's Motrin Lawsuit
Health officials are investigating reports that bottles containing Children's Motrin grape chewable ibuprofen tablets actually are filled with adult doses of Tylenol, a serious health risk to children. The lot was distributed nationwide between February 5, 2004 and April 1, 2004, says drugmaker McNeil Consumer & Specialty Pharmaceuticals. Parents should be on the lookout for bottles with the lot number "Exp 1/06 JAM108." The eight-hour extended release Tylenol Geltabs are red-and-white and contain an adult dose of acetaminophen. Click here for more information regarding Children's Motrinc lawsuit

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FOSAMAX LAWYER
Free Claim Evaluation
The U.S. Food and Drug Administration asked Merck to add a warning to Fosamax's label in August of 2004 and it has yet to comply with that request. In a statement, Merck said that in all of its clinical trials of Fosamax, which have included more than 17,000 patients, it has not had any reports of osteonecrosis of the jaw. Merck said that there have been reports of patients taking Fosamax developing the condition but that doesn't necessarily mean the drug caused it.

Fosamax is taken by nearly 10 million men and women. Fosamax is Merck's second best-selling drug with last year's revenue at $3.2 billion.

If you or a loved one have suffered from the dangerous side effects of Fosamax and wish to know if you should file a lawsuit, you should consider receiving a free legal evaluation from an experienced Fosamax lawyer. For a free evaluation of your situation please complete the following form and a Fosamax attorney will contact you promptly -- free of charge.

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BEXTRA ATTORNEY
Free Claim Evaluation
If you or a loved one suffered a serious side effect such as a stroke, a heart attack, or Stevens-Johnson Syndrome/Toxic Epidermal Necrosis while taking Bextra, our lawyers are ready to help you. Thousands of law firms will be involved in the effort to get justice for the many victims of Bextra – don't trust your case to just any lawyer. Williams Bailey has the resources and expertise needed to represent you in a lawsuit against Pfizer.

On April 7th, after pressure from the Food and Drug Administration (FDA), Pfizer withdrew its painkiller Bextra from the market. Bextra (valdecoxib) is a nonsteroidal anti-inflammatory drug (NSAID) that causes less stomach irritation than other NSAIDs. It was originally intended as a simple pain reliever, prescribed most commonly for arthritis, but has been found to increase the risk of heart attack and stroke, as well as the severe allergic reaction called Stevens-Johnson Syndrome/Toxic Epidermal Necrosis.

If you or a loved one suffered a serious side effect such as a stroke, a heart attack, or SJS or TEN while taking Bextra, please contact us to file a claim.

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RENU MOISTURELOC ATTORNEY
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After health officials linked its product to a serious eye infection, Bausch & Lomb announced the suspension of shipments of its contact solution ReNu with MoistureLoc on April 10, 2006. Health officials with the U.S. Food and Drug Administration and the U.S. Centers for Disease Control and Prevention warned of increasing numbers of a serious fungal infection of the eye in those who were contact lenses, which could lead to blindness.

In February, Bausch & Lomb stopped sale of ReNu in Hong Kong and Singapore because of an increase in the fungal infection, but both the FDA and the CDC said there is not enough evidence to withdraw the product from the U.S. market. However, on April 13, 2006, Bausch & Lomb warned consumers not to use the product and asked retailers to pull the product from their shelves until investigations conclude.

If you or a loved one developed an infection as a result of Bausch & Lomb ReNu MoistureLoc contact lens solution, you should consider receiving a free legal evaluation from an experienced injury lawyer.

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CHILDREN'S MOTRIN LAWYER
Free Claim Evaluation
If you have a child who has taken Children's Motrin containing an adult dose of acetaminophen, it may be important to contact an attorney who can help you protect your legal rights. Please keep in mind that there may be time limits within which you must commence suit

Click Here: Free Children's Motrin Lawsuit Case Evaluation


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