Insight from attorney Scott Weinstein of Morgan & Morgan, PA was featured in a recent AP article about the potential health risks associated with denture cream use. The article relates the story of one of Mr. Weinstein's clients, a Florida resident named Ronald Beaver. Mr. Beaver had ill fitting dentures and often used large amounts of PoliGrip denture cream to secure them. Unfortunately, the high levels of zinc he ingested from the denture cream made his copper levels drop, causing weakness and a serious blood disorder.

Zinc is a common ingredient in denture creams because it helps improve the cream's adhesive power. However, a study published in the medical journal Neurology in 2008 linked denture cream use to high zinc levels. In turn, toxic zinc levels can lead to zinc poisoning, copper depletion, and a neurological condition known as neuropathy. However, neither the denture cream manufacturers nor the Food and Drug Administration (FDA) have issued warnings about these possible side effects.

Now, Mr. Beaver and hundreds of other denture cream users from around the country who suffered similar problems are suing GlaxoSmithKline (manufacturer of PoliGrip) and Proctor & Gamble Co. (manufacturer of Fixodent). In June, at least 18 individual cases were consolidated in a multidistrict litigation (MDL) before U.S. District Judge Cecilia M. Altonaga in the Southern District of Florida. Mr. Weinstein, who is the Managing Partner of Morgan & Morgan's nationwide Mass Tort & Class Action Department, has been appointed both Co-Lead counsel and Plaintiff's liaison counsel in the denture cream zinc poisoning MDL.

As Co-Lead Counsel, Mr. Weinstein is responsible for representing Ronald Beaver and all of the other MDL plaintiffs in the pre-trial proceedings. This includes responding to inquiries from the court, submitting and arguing motions, examining witnesses at hearings, and negotiating potential settlements. Andy Alonso of Parker Waichman & Alonso LLP, who was also named Co-Lead Counsel, and the Plaintiffs' Steering Committee (PSC) will assist in conducting discovery and other work for the benefit for all plaintiffs.

The denture cream attorneys at Morgan & Morgan offer a Free Case Review for denture cream users who believe they may be suffering from zinc poisoning. If you need additional information about the potential health risks associated with denture cream use and the legal rights of individuals affected by denture cream zinc poisoning, please visit Morgan & Morgan's Denture Cream Zinc Poisoning Resource Center.

About Morgan & Morgan

Morgan & Morgan is one of the largest Personal Injury law firms in the country with offices nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

Attorney Scott Weinstein of Morgan & Morgan, PA has been named to the Chinese drywall Plaintiffs' Steering Committee (PSC). Weinstein and the other members of the Plaintiffs' Steering Committee were appointed by Judge Eldon E. Fallon, who is presiding over the Chinese drywall multidistrict litigation (MDL) in the Eastern District of Louisiana. All Chinese drywall lawsuits pending in federal court have been consolidated at this venue for pretrial proceedings.

Members of the Chinese drywall PSC are responsible for conducting and coordinating the discovery stage of the case, examining witnesses and introducing evidence at hearings, and acting as a spokesperson for all plaintiffs at pretrial proceedings. In addition, the Committee will negotiate with the defendants and explore settlement options. Appointments to the Chinese drywall PSC were based on four main criteria: a willingness to commit to a time consuming project, the ability to cooperate with others, professional experience in this type of litigation, and a willingness to commit the resources necessary to pursue this matter. Mr. Weinstein has served in leadership positions in many consumer class actions around the country, making him well qualified for this role. Appointments to the PSC expire one year from the date of Judge Fallon's order, but appointees may apply to be reappointed when their term expires.

All of the cases in the Chinese drywall MDL involve claims that defective drywall imported from China emits a strong sulfurous smell and corrodes electrical wiring. This makes living conditions unpleasant for residents and results in extensive damage to air conditioning units and other electrical appliances. In addition, there are concerns that exposure to the fumes emitted by the drywall may cause health problems, including headache, cough, and difficulty breathing. However, authorities are still investigating whether Chinese drywall can be definitively linked to any adverse medical conditions. If these Chinese drywall cases do not settle during the pretrial proceedings, they will be sent back to the district where they were originally filed for trial.

To learn more about defective Chinese drywall, visit Morgan & Morgan's Chinese Drywall Resource Center. A comprehensive collection of articles related to Chinese drywall is available on this webpage for consumers to review. Topics include signs of defective drywall, Chinese drywall class action lawsuits, Chinese drywall health risks, and a frequently asked questions section. If you believe that your home was built with Chinese drywall, complete the Free Case Evaluation form to learn more about your legal rights.

About Morgan & Morgan

Morgan & Morgan is one of the largest Personal Injury law firms in the country with offices nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

Attorney Scott Weinstein of Morgan & Morgan, PA has been featured in Thomas Brom's article, "Great Drywall of China," which ran in the August issue of California Lawyer. The article recalls a scene in which Weinstein brought a sample of defective Chinese drywall to a litigation conference. As the sample was passed around the room, the sulfur fumes became strong and some attendees were reluctant to even touch the sample. Throughout the rest of the piece, quotes and insights from Weinstein reveal the struggles faced by homeowners whose homes were built with Chinese drywall, as well the challenges faced by the attorneys who are trying to recover compensation for them.

If you are interested in reading the full article, visit this link: "Great Drywall of China".

The Chinese drywall problem began during the housing boom of 2004-2007. U.S. drywall suppliers could not keep up with demand during this period, so thousands of homes across the country were built with wallboard imported from China. Studies have shown that the Chinese wallboard contains various sulfur compounds and ten times the amount of strontium that is found in drywall produced domestically. As a result, the drywall emits a strong sulfurous smell, similar to the smell of rotten eggs. It has also been alleged that the sulfurous gases corrode wiring, causing damage to air conditioning units and other electrical appliances.

The first Chinese drywall lawsuit was filed in February 2009, and hundreds more were filed in the following months. In June 2009, the United States Judicial Panel on Multidistrict Litigation issued an order centralizing In re: Chinese-Manufactured Drywall Products Liability Litigation, MDL 2047. The MDL consolidated at least ten Chinese drywall lawsuits in the Eastern District of Louisiana before Judge Eldon E. Fallon. Scott Weinstein has been named to the Plaintiffs' Steering Committee for the Chinese drywall MDL.

If you are interested in learning more about Chinese drywall, visit Morgan & Morgan's Defective Chinese Drywall Resource Center. Informational articles about the signs and causes of defective Chinese drywall, health risks, property damage issues, class action lawsuits, and more are available on this webpage for consumers to review. If you believe defective drywall may have been used in the construction of your home, fill out the Free Case Evaluation form to learn more about your rights and legal options.

About Morgan & Morgan

Morgan & Morgan is one of the largest Personal Injury law firms in the country with offices nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

According to an order issued by U.S. District Judge Eldon Fallon on July 27, 2009, attorney Scott Weinstein of Morgan & Morgan, PA has been named to the Plaintiffs' Steering Committee for the Chinese drywall multidistrict litigation (MDL). Weinstein and the other members of the Plaintiffs' Steering Committee will be responsible for conducting and coordinating the discovery stage of this case, examining witnesses and introducing evidence at hearings, and handling various other tasks related to the pretrial proceedings.

Between 2004 and 2007, thousands of homes throughout the country were built with Chinese drywall after a construction boom and several hurricanes led to a shortage in domestic drywall. All of the cases in the Chinese drywall MDL involve claims that defective wallboard imported from China was made with materials that contain high levels of sulfur compounds. As a result, the drywall emits a strong sulfurous smell, similar to the smell of rotten eggs. Plaintiffs also claim the sulfurous gases corrode wiring, causing damage to air conditioning units and other electrical appliances. In addition, there are concerns that exposure to the fumes may cause health problems.

In June 2009, the United States Judicial Panel on Multidistrict Litigation issued an order centralizing In re: Chinese-Manufactured Drywall Products Liability Litigation, MDL 2047. The MDL consolidated at least ten Chinese drywall lawsuits in the Eastern District of Louisiana before Judge Fallon in order to conserve resources and avoid duplicate discovery and inconsistent rulings. If these cases do not settle during the pretrial proceedings, they will be sent back to the district where they were originally filed for trial.

To learn more about Chinese drywall, visit Morgan & Morgan's Defective Chinese Drywall Resource Center. Informational articles about the signs and causes of defective Chinese drywall, the manufacturing and building companies linked to the defective wallboard, and the Chinese drywall class action lawsuit filed by Morgan & Morgan are available on this webpage for consumers to review.

About Morgan & Morgan

Morgan & Morgan is one of the largest Personal Injury law firms in the country with offices nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

According to an order issued by U.S. District Judge Cecilia M. Altonaga on July 13, 2009, attorney Scott Weinstein of Morgan & Morgan, PA has been designated Co-Lead Counsel for plaintiffs in the denture cream zinc poisoning multidistrict litigation (MDL). Along with Andy Alonso of Parker, Waichman & Alonso LLP, Weinstein will handle the pre-trial proceedings for all MDL plaintiffs who allegedly suffered zinc poisoning and other injuries after using Fixodent and Super Poligrip denture creams. Weinstein and Alonso will be responsible for responding to inquiries from the court, submitting and arguing motions, examining witnesses at hearings, and negotiating potential settlements.

Last month, the Judicial Panel on Multidistrict Litigation (JPML) issued an order centralizing In re: Denture Cream Product Liability Litigation, MDL-2051, in the Southern District of Florida before Judge Altonaga. There are currently at least 18 individual cases consolidated in the multidistrict litigation, including 14 denture cream lawsuits against GlaxoSmithKline PLC (manufacturer of Super PoliGrip) and four lawsuits against Proctor & Gamble (manufacturer of Fixodent). If the cases consolidated in the MDL are not settled during the pretrial litigation, they will be transferred back to the court where they were originally filed to be tried individually.

A study published last year in the medical journal Neurology linked "chronic and excessive" use of denture cream to high zinc levels. Toxic zinc levels can result in copper depletion and a nerve disorder known as neuropathy. Symptoms of zinc poisoning that denture cream users should be aware of include poor balance, tingling sensation, and pain in the extremities. Weakness, numbness, and loss of sensation can also be signs of toxic zinc levels. Denture cream users who experience these symptoms should speak to a doctor as soon as possible in order to ensure that they receive the proper testing and treatment.

For more information about denture cream zinc poisoning, visit Morgan & Morgan's Denture Cream Zinc Poisoning Resources. Informational articles about denture cream lawsuits, denture cream side effects, zinc poisoning, neuropathy, copper deficiency, and additional related topics are available on this page for consumers to review.

About Morgan & Morgan

Morgan & Morgan is one of the largest Personal Injury law firms in the country with offices nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

The attorneys at Morgan & Morgan (ForThePeople.com) are alerting consumers that the Food & Drug Administration has issued a public health advisory that use of Zicam Cold Remedy nasal products should be discontinued. These products, manufactured by Matrixx Initiatives, are zinc-containing nasal cold remedies used to reduce the duration and severity of cold symptoms. However, they have been found to cause a long lasting or permanent loss of sense of smell, which is referred to as anosmia.

The products associated with this Public Health Advisory are:

• Zicam Cold Remedy Nasal Gel (15mL, NDC 62750-003-10)
• Zicam Cold Remedy Swabs (20 swabs, NDC 67250-003-20)
• Zicam Cold Remedy Swabs, Kids Size (20 swabs, NDC 67250-003-21)

Zicam is an intranasal zinc solution. Zinc can cause a condition called anosmia, which results in loss of the sense of smell and partial reduction of the sense of taste. Since Zicam Cold Remedy Nasal Gel was introduced in 1999, the FDA has received more than 130 reports of loss of sense of smell associated with the use of Zicam zinc-containing intranasal products. While some people experienced a loss of sense of smell after the first dose, others reported this side effect after multiple uses of the products. Loss of the sense of smell can adversely affect one's quality of life and limits an individual's ability to detect the scent of gas, smoke, chemicals, and other harmful fumes.

The FDA recommends that consumers stop using these products and discard them. Individuals who have experienced a loss of sense of smell after using any of the affected Zicam products should contact a health care professional.

To learn more about the harmful side effects of Zicam, visit Morgan & Morgan's Zicam Lawsuits page. If you or a loved one lost your sense of smell after using a Zicam product, you may be entitled to financial compensation. Fill out the free case evaluation form to learn more about your legal rights and options if you have experienced anosmia after using a Zicam intranasal zinc product. Morgan & Morgan's Zicam lawyers are experienced in litigating dangerous and defective drug cases and have the resources and knowledge to pursue justice on your behalf.

The attorneys at Morgan & Morgan are warning consumers that the psoriasis drug Raptiva has been linked to serious and potentially fatal health problems, including progressive multifocal leukoencephalopathy.

Raptiva (efalizumab) is a drug that was introduced in 2003 to treat psoriasis. Psoriasis, which is characterized by red scaly patches on the skin, is an autoimmune disease which affects the skin and joints. Raptiva is an injection that is given once a week to treat moderate to severe psoriasis in adults by suppressing T-cells (blood cells that help fight infection) in the immune system. However, by suppressing the immune system, Raptiva puts patients at an increased risk for serious infection. In October 2008, Raptiva received the Food and Drug Administration's strongest warning (a "black box" warning) due to the risk of life threatening infections associated with its use.

Health problems that have been linked to the use of Raptiva include:

• Viral Meningitis
• Bacterial Sepsis
• Encephalopathy
• Lymphoma
• Progressive Multifocal Leukoencephalopathy (PML)

In February 2009, the FDA issued a public health advisory statement that identified Raptiva as a risk factor for the development of a severe and fatal condition known as progressive multifocal leukoencephalopathy (PML). The FDA has received reports of 3 confirmed and 1 possible case of PML in patients using Raptiva. All four of these patients were treated with Raptiva for over three years, and three of the four have died.

Progressive multifocal leukoencephalopathy is a rare brain infection caused by a virus that affects the central nervous system. It often occurs in people with weakened immune systems and can result in irreversible neurologic damage and death. Symptoms of PML include loss of coordination, progressive weakness, paralysis, vision loss, fatigue, memory loss, difficulty with speech, and disorientation.

If you or a loved one has taken Raptiva and been diagnosed with Progressive Multifocal Leukoencephalopathy or any other type of serious infection, you may be entitled to compensation. Visit the Raptiva Recall Information Center to learn more about the health risks associated with Raptiva and the rights of patients who have been injured by this drug. Fill out the Free Case Evaluation form to find out if you are eligible to participate in a Raptiva lawsuit. Morgan & Morgan's Raptiva lawyers are experienced in litigating dangerous and defective drug cases and have the resources and knowledge to pursue justice on your behalf.

About Morgan & Morgan

Morgan & Morgan is one of the largest Personal Injury law firms in the country with offices nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

The attorneys at Morgan & Morgan are warning consumers that Yasmin (also known as Yaz) birth control pills have been linked to serious side effects, including heart attack, stroke, and death. Yaz and Yasmin, as well as the generic equivalent Ocella, are daily oral contraceptives designed to prevent pregnancy.

Yasmin is one of the most popular oral contraceptives on the market, and it is the first type of birth control to contain a different kind of hormone, called drsp or drospirenone. Although the manufacturers of this drug claim that it is as safe as other types of accepted birth control pills on the market, drospirenone can increase the potassium levels of users. Increased potassium levels can cause health problems and are particularly dangerous for people with kidney, liver or adrenal disease. Serious side effects that have been linked to the use of Yaz/Yasmin birth control pills include:

• Heart attack
• Cardiac arrhythmia
• Blood clot
• Deep Vein Thrombosis (DVT)
• Pulmonary Embolism (PE)
• Stroke
• Gallbladder disease
• Benign liver tumor
• Sudden death

Risk factors for these side effects include preexisting heart or cardiovascular problems, diabetes, high blood pressure, and obesity. Less serious side effects of Yaz/Yasmin include upper respiratory infection, headache, nausea, diarrhea, vomiting, vaginitis, urinary tract infection, intermenstrual bleeding, dizziness and pain.

The Food and Drug Administration (FDA) has repeatedly reprimanded Bayer Healthcare Pharmaceuticals (the manufacturers of Yaz/Yasmin) for marketing this drug in a way that minimizes these serious side effects and misleads women about the safety of this new type of birth control. However, the drug has not yet been recalled by the FDA or by its manufacturer.

If you or a loved one has suffered a heart attack, stroke, or any other serious health problem that may have been caused by Yasmin, you may be entitled to compensation. Visit the Yaz/Yasmin Side Effects Information Center and fill out the free case evaluation form to find out if you are eligible to file a Yaz lawsuit. Morgan & Morgan's Yasmin lawyers are experienced in litigating dangerous and defective drug cases and have the resources and knowledge to pursue justice on your behalf.

About Morgan & Morgan

Morgan & Morgan is one of the largest Personal Injury law firms in the country with offices nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

The attorneys at Morgan & Morgan (ForThePeople.com) are currently investigating claims of zinc poisoning and neuropathy caused by denture cream use.

Zinc is an ingredient in several popular denture cream brands, including Poligrip and Fixodent. While a small amount of zinc is necessary for a healthy and balanced diet, in excess it can result in copper depletion and a nerve disorder known as neuropathy. A study published last year in the medical journal Neurology linked "chronic and excessive" use of denture creams, including Super Poligrip and Fixodent, to high zinc levels and neurological problems.

Symptoms of zinc poisoning that denture cream users should be aware of include poor balance, tingling sensation, and pain in the extremities. Weakness, numbness, and loss of sensation can also be signs of toxic zinc levels. Denture cream users who experience these symptoms should speak to a doctor as soon as possible in order to ensure that they receive the proper testing and treatment.

A number of lawsuits have already been filed against GlaxoSmithKline (manufacturer of PoliGrip) and Proctor & Gamble (manufacturer of Fixodent) on behalf of consumers nationwide who have suffered from zinc poisoning and neuropathy due to denture cream use. Morgan & Morgan's denture cream attorneys are committed to holding denture cream manufacturers accountable for their negligence and helping victims of zinc poisoning obtain fair compensation for their injuries.

If you use a denture adhesive cream that contains zinc, such as Poligrip or Fixodent, you may be at risk for zinc poisoning. To learn more about the link between denture adhesive creams and zinc poisoning, visit Morgan & Morgan's Denture Cream Zinc Poisoning Resource Page. Informational articles about denture cream lawsuits, denture cream side effects, zinc poisoning, neuropathy, copper deficiency, and additional related topics are available on this page for consumers to review.

Morgan & Morgan's denture cream lawyers offer a free case evaluation for those who may have been injured by denture cream use. Individuals who are eligible to participate in a denture cream lawsuit may be eligible to receive compensation for medical expenses, loss of income, pain and suffering, and other damages.

About Morgan & Morgan

Morgan & Morgan is one of the leading plaintiff's law firms in the country, representing clients nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

The attorneys at Morgan & Morgan are currently investigating cases of acute phosphate nephropathy and other kidney problems caused by Fleet Phospho-soda. Fleet Phospho-soda is an oral sodium phosphate solution, which was commonly used as a laxative and to cleanse the bowel prior to a colonoscopy or bowel surgery.

Fleet Phospho-soda achieves laxative action by drawing fluids from other parts of the body into the colon. This can cause serious side effects, including acute phosphate nephropathy (APN). APN occurs when deposits of calcium-phosphate crystals become trapped in the renal (kidney) tubules. The entrapment of these crystals can lead to permanent kidney function impairment, and dialysis or a kidney transplant may be required to treat it. Symptoms of APN include malaise, lethargy, decreased urine, and swelling of the ankles, feet and legs. Blood tests can be used to formally diagnose APN. Other harmful side effects associated with the use of oral sodium phosphates include kidney failure and chronic kidney disease.

People over the age of 55 and people who are hypovolemic or have decreased intravascular volume are at an increased risk for developing these problems. Additional risk factors that may increase the potential for dangerous Fleet Phospho-soda side effects include: • Preexisting kidney disease • Bowel obstruction • Active colitis • Use of medications that affect renal perfusion or function (such as diuretics, angiotensin converting enzyme inhibitors, angiotensin receptor blockers, and nonsteroidal anti-inflammatory drugs)

The risk of kidney damage from oral sodium phosphate products was first reported in 2003, and the FDA released a paper describing the occurrence of APN as a serious adverse event associated with oral sodium phosphate products in 2006. However, C.B. Fleet continued to market Fleet Phospho-soda as a bowel cleanser without adequate warnings until December 2008, when it voluntarily recalled the product following an official FDA alert. C.B. Fleet is currently facing a number of Fleet Phospho-soda lawsuits filed by individuals who suffered kidney problems after using a Fleet Phospho-soda bowel cleansing solution.

If you or a loved one developed acute phosphate nephropathy or any other form of kidney damage after taking Fleet Phospho-soda, you may be entitled to compensation. Visit Morgan & Morgan's Fleet Phospho Soda Recall Information Center and fill out the free case evaluation form to find out if you are eligible to file a Fleet Phospho-soda lawsuit. Morgan & Morgan's Fleet Phospho-soda lawyers are experienced in litigating dangerous and defective drug cases and have the resources and knowledge to pursue justice on your behalf.

About Morgan & Morgan

Morgan & Morgan is one of the largest Personal Injury law firms in the country with offices nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

The attorneys at Morgan & Morgan are alerting consumers that as of May 1, 2009, the Food & Drug Administration (FDA) is warning consumers to immediately stop using Hydroxycut products. Hydroxycut products, which are dietary supplements manufactured by Iovate Health Sciences, Inc., have been linked to serious liver injuries and at least one death.

This warning was issued after the FDA received 23 reports of serious health problems attributed to Hydroxycut use. The health problems reported include jaundice, elevated liver enzymes, and liver damage. In some cases, the liver damage was so severe that a liver transplant was required. Liver injury occurred even when victims were not exceeding the dosage recommended on the bottle. In addition, one death due to liver failure has been reported to the FDA. Other health problems linked to Hydroxycut use include seizures, cardiovascular disorders, and rhabdomyolysis.

Although the serious liver problems suffered by some Hydroxycut users appear to be rare, anyone taking these products could be at risk. As a result, Iovate has agreed to recall the following Hydroxycut products from the market:

• Hydroxycut Regular Rapid Release Caplets
• Hydroxycut Caffeine-Free Rapid Release Caplets
• Hydroxycut Hardcore Liquid Caplets
• Hydroxycut Max Liquid Caplets
• Hydroxycut Regular Drink Packets
• Hydroxycut Caffeine-Free Drink Packets
• Hydroxycut Hardcore Drink Packets (Ignition Stix)
• Hydroxycut Max Drink Packets
• Hydroxycut Liquid Shots
• Hydroxycut Hardcore RTDs (Ready-to-Drink)
• Hydroxycut Max Aqua Shed
• Hydroxycut 24
• Hydroxycut Carb Control
• Hydroxycut Natural

Jaundice and brown urine are common symptoms of liver disease. Other symptoms include nausea, vomiting, light-colored stools, unusual tiredness, weakness, stomach pain, or loss of appetite. If you have used Hydroxycut and are experiencing any of these symptoms, you should see your healthcare provider as soon as possible. In addition, Morgan & Morgan's Hydroxycut lawyers are offering a free legal consultation for victims who are interested in learning more about their legal rights. For more information, visit Morgan & Morgan's Hydroxycut Recall Alert. If you have developed liver damage or other serious health problems that you believe are related to the use of Hydroxycut, you may be entitled to compensation. Fill out the free case evaluation form on the right side of the page to learn how Morgan & Morgan's Hydroxycut lawyers can help you.

About Morgan & Morgan Morgan & Morgan is one of the largest Personal Injury law firms in the country with offices nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

The attorneys of Morgan & Morgan (ForThePeople.com) are currently investigating cases of tardive dyskinesia caused by the long term use of Reglan. Tardive dyskinesia is a serious and potentially irreversible neurological disorder characterized by involuntary, repetitive movements in the face and extremities.

Reglan (generic name Metoclopramide) is a prescription drug used to treat gastrointestinal disorders, such as gastroesophageal reflux disease (GERD), acid reflux disease, and heart burn. It has also been prescribed for women who are pregnant and experiencing morning sickness, people undergoing cancer treatment, infants and children, and post-operative patients. Metoclopramide is available in several forms, including Reglan tablets, Reglan oral disintegrating tablets, metoclopramide oral solution, and Reglan injection.

While the FDA has approved Reglan only for short-term use, many patients are being prescribed the medication for 12 months or greater. It is critical that Reglan is used only for short-term relief of gastrointestinal problems when other treatments have failed. In February 2009, the Food and Drug Administration issued a black box warning (its strongest warning) for Reglan and other metoclopramide-containing drugs due to the risk of tardive dyskinesia for people who take the drug in high doses or over a long period of time.

Symptoms of tardive dyskinesia include involuntary movements of the tongue, lips or jaw, as well as facial grimacing and rapid eye blinking. Rapid, involuntary movements of the fingers, hands, arms, shoulders, legs, and trunk are additional symptoms of this condition. These symptoms are rarely reversible and there are no effective treatments available for tardive dyskinesia at this time. The elderly and people who have been on the drug for a long period of time are at the highest risk for developing these problems.

To learn more about the risks associated with long term use of Reglan, visit Morgan & Morgan's Reglan Consumer Alert. If you or a loved one has experienced any of the symptoms of tardive dyskinesia after using Reglan, fill out the free case evaluation form to find out if you can participate in a lawsuit against the manufacturers of this drug. The attorneys at Morgan & Morgan are dedicated to protecting the rights of individuals who have been harmed by defective and dangerous drugs.

About Morgan & Morgan

Morgan & Morgan is one of the largest Personal Injury law firms in the country with offices nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

The product liability attorneys at Morgan & Morgan are alerting consumers that on March 31, 2009, the Consumer Product Safety Commission (CPSC) issued a recall on all Yamaha Rhino 450 and 660 model vehicles. This recall affects approximately 120,000 off-road recreational vehicles and was issued because of alleged design flaws that make these ATVs unstable and susceptible to rollover accidents.

All terrain vehicles, also known as ATVs, quads, or four wheelers, are used for recreational off-road riding. The Yamaha Rhino ATVs are being recalled due to the fact that accidents involving the 450 and 660 models have resulted in 46 deaths and hundreds of injuries since 2003. Many of these accidents were rollovers that involved turns on level terrain at relatively low speeds.

Yamaha Motor Corp. U.S.A., of Cypress, Calif., is offering a free repair program to address vehicle safety and stability issues that contributed to these ATV accidents. The repairs are designed to reduce the risk of rollover accidents, improve handling, and keep riders' limbs inside the vehicles. The CPSC recommends that consumers stop using these popular recreational vehicles until the necessary repairs have been completed by a local dealer. In addition, sales of these models have been suspended. Yamaha is also voluntarily implementing the same repair program and suspension of sale for the Rhino 700 model.

For more information about the Yamaha Rhino recall, visit Morgan & Morgan's ATV Rollover Accident Information page. If you or a loved one has been injured or killed in an ATV accident involving one of the recalled Yamaha Rhino models, the lawyers at Morgan & Morgan urge you to contact one of their ATV recall lawyers as soon as possible to protect your legal rights. A free, no obligation case evaluation form is available on their website.

About Morgan & Morgan

Morgan & Morgan is one of the leading plaintiff's law firms in the country, representing clients nationwide. They are committed to serving the people, not the powerful. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

The denture cream zinc poisoning consumer resources on ForThePeople.com, the website for national plaintiff's firm Morgan & Morgan, have been updated. New information about the health risks associated with denture cream use is now available on ForThePeople.com for users of Fixodent, PoliGrip, Super PoliGrip, and other denture cream brands that contain zinc.

Denture cream users who are experiencing numbness, tingling, unexplained pain or weakness, and poor balance may be suffering from zinc poisoning. The neurological damage caused by zinc poisoning can be permanent and debilitating if it is not detected early and treated effectively. A blood test can determine if abnormal zinc and copper levels are present. Detailed articles with information about denture cream side effects, zinc poisoning, copper deficiency, and neuropathy are now available on ForThePeople.com for those who want to learn more about the link between denture cream use and zinc toxicity. Information about the findings of medical researchers who studied denture cream users that suffered from neuropathy and other neurological problems associated with zinc poisoning is also featured on the site.

People who suffer from zinc poisoning and neuropathy caused by denture cream brands such as PoliGrip, Super PoliGrip, or Fixodent may be entitled to file a denture cream lawsuit. Denture cream lawsuits are typically filed against the denture cream manufacturer and allege that the manufacturer failed to warn consumers about the zinc poisoning and copper deficiency risks associated with denture cream use. Morgan & Morgan's denture cream lawyers are dedicated to helping victims of zinc poisoning obtain fair compensation for their injuries and holding denture cream manufacturers accountable for their negligence.

If you use denture adhesive cream regularly, you may be at risk for zinc poisoning. For more information about denture adhesive creams and zinc poisoning, visit Morgan & Morgan's Denture Cream Zinc Poisoning Consumer Resources. Morgan & Morgan's denture cream attorneys offer a free case evaluation for those who have been injured by denture cream use. Individuals who file a denture cream lawsuit may be eligible to receive compensation for medical expenses, loss of income, pain and suffering, and other damages.

About Morgan & Morgan

Morgan & Morgan is one of the leading plaintiff's law firms in the country, representing clients nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.

The attorneys at Morgan & Morgan (ForThePeople.com) are currently investigated claims of zinc poisoning and neuropathy caused by denture cream use. A study published last year in the medical journal Neurology linked "chronic and excessive" use of denture creams, including Super Poligrip and Fixodent, to high zinc levels and neurological problems.

Zinc is an ingredient in several popular denture cream brands. While a small amount of zinc is necessary for a healthy and balanced diet, in excess it can result in copper depletion and serious neurological problems. Exposure to toxic levels of zinc can cause weakness in the extremities, numbness, and loss of sensation. Symptoms of zinc poisoning that denture cream users should be aware of include poor balance, tingling sensation, and pain in the extremities. A feeling of wearing gloves or socks when the skin is bare is another sign that may indicate zinc poisoning. Severe cases of zinc poisoning can lead to neuropathy, a condition that affects the nerves. Although zinc levels may eventually return to normal after an individual stops using denture cream, the neurological damage caused by zinc poisoning can be irreversible. A blood test can determine whether denture cream users have toxic levels of zinc in their systems.

The study published in Neurology was carried out by researchers at the University of Texas at Dallas and involved four patients, including a 42-year-old woman who used about three tubes of denture cream per week and suffered from extreme weakness and reduced sensation in her hands. The Food and Drug Administration does not require denture cream manufacturers to disclose the potential toxic effects of denture cream use, so many of the 35 million denture cream users in Americans are unaware of the health hazard posed by the zinc ingredient in these products.

If you use denture adhesive cream regularly, you may be at risk for zinc poisoning. For more information about the health risks associated with denture cream use, visit the Denture Cream and Zinc Poisoning Resources on ForThePeople.com. Morgan & Morgan's product liability attorneys offer a free case evaluation for those who have been injured by denture cream use and wish to learn more about their legal options.

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Morgan & Morgan is one of the leading plaintiff's law firms in the country, representing clients nationwide. The firm handles product liability cases, personal injury cases, and medical malpractice cases, as well as claims against drug and medical device manufacturers. Visit ForThePeople.com for a free case evaluation and information about your legal rights.