Recent Blog Posts

Can I File an Actos Lawsuit if I Have Been Diagnosed with Bladder Cancer

National Drug Recall Injury Lawyer — Tue, 24 Jan 2012 03:44:00 GMT

Actos is a drug that has been used to regulate sugar levels in the blood system for over 13 years throughout the United States. When it was first approved by the FDA in 1999, the drug came into wide usage for folks suffering from Type II diabetes. Actos came along with the traditional set of side effects, including nasea, dry skin, dry eyes, and other minor effects. However, our Actos injury lawyers are now filing lawsuits on behalf of persons who have developed bladder cancer as a result of taking Actos. If you are taking this medication and are experiencing painful urination, blood in urination, and other serious side effects, it is critical that you address these issues with your treating physician.

If you have developed bladder cancer, a drug recall attorney can investigate your medical records and determine whether you have sufficient evidence to file a lawsuit for product liability or product defect. Product liability claims are based on allegations that a drug manufacturer knew, or should have known, that a particular prescription medication causes a particular type of injury. In the case of Actos, that is believed to be bladder cancer.

In the event you have an Actos claim, you may be entitled to compensation which includes damages for economic and non-economic damages. In claiming damages, it is important to determine all of the ways in which a particular product, and resulting injury or trauma, has caused you harm. There are certain statute of limitations in place that determine how long a victim has to file an Actos compensation claim. Those time limitations vary by state, so it is important to consult with an attorney to address the particular time left in your case in which you are permitted to file a lawsuit.

To determine if you have an Actos bladder cancer lawsuit, contact an attorney at (866) 840-3636 to ask the important questions, such as 1) do I have a claim 2) what am I entitled to, and 3) what will it cost me to get started? Our Actos attorneys do not charge any attorney's fees unless we are successful in winning your case. It costs nothing to a client for our national law firm to investigate a potential case to determine whether there is enough evidence to seek compensation.

How do I know if I have a drug recall injury claim for compensation?

Nationwide Drug Recall Injury Lawyer — Tue, 30 Aug 2011 22:17:00 GMT

Whether it is a Lexapro birth defect claim, or a DePuy defective hip lawsuit claim, our nationwide drug defect and medical device defect lawyers field calls every day from persons inquiring as to whether they have a case. These product liability cases are extremely complex and require a thorough investigation from the start. Our injury law firm spends time and resources investigating the merits of each case that we are presented with. This includes a review of medical records and other supporting documentation and a panel review by our physician expert witnesses. This ensures that each claim is prepared in a manner in which will make chances at success at trial quite high.

Anyone who suspects that a prescription drug or medical device has caused them injury is encouraged to preserve all documentation and evidence necessary for us to perform a review of the case. This includes the pill bottles themselves, the prescription and/or medical records, and and correspondence from a manufacturer. For example, some DePuy hip implant victims are receiving letters from the manufacturer regarding the surgery and a possible need for corrective revision. We recommend that you keep these documents safe and do not respond in writing to the manufacturer without first consulting with an experienced product liability attorney.

A nationwide product liability lawyer should review your case free of charge. The only time attorneys fees should be charged is if the lawyer or law firm takes on your case and is able to obtain a settlement or jury verdict in your favor. This is also known as the "contingency fee contract," and all reputable personal injury lawyers use this type of agreement with clients. It is a system that works great for injury victims becasue each client has the opportunity to hire a great lawyer without any personal financial "out of pocket" risk.

If you have questions about a drug defect claim or claim for compensation based on a defective medical implant, contact a drug recall injury lawyer immediately for a free consultation.

Missouri Lawyers Are Filing Lexapro Heart Defect Claims

Lexapro heart defect lawyer — Mon, 25 Jul 2011 01:26:00 GMT

Our Lexapro heart defect lawyers are vigorously investigating claims throughout the country that Lexapro causes serious heart defects in newborn children. The manufacturer of Lexapro is a Missouri based company, such that these claims are best filed in Missouri State Court, even if the victim lives outside of Missouri. Many firms automatically file these claims in federal court, if they are not a Missouri based law firm. We feel that federal court is not in the best interest for most mothers whose newborn child has a complex heart defect claim.

Our Missouri drug defect law firm is particularly vested in Lexapro litigation. Why? Because we take the claim of a young child particularly serious, as these newborn children are victims of a potentially permanent heart defect. Our birth defect lawyers supports many children's charities, including St. Judes and the Fondation for Children with Cancer. We do this because we are in business to protect people, especially children.

If you were a pregnant and took Lexapro, there is a possibility that any congenital heart defects of your child can be related to this particular drug. Lexapro is a Selective Serotonin Re-uptake Inhibitor (SSRI), and like many other SSRIs, is used to treat pyschological disorders. If you are pregnant, it is absolutely critical that you consult with your maternity doctor and disclose all current medications that you are taking. Also, exercise care and research the side effects associated with ANY prescription medication taken during pregnancy.

A Lexapro heart defect attorney at Schultz & Myers law firm will investigate your claim and provide you with answers. There are no attorneys fees if we determine that you do not have a case. With offices in St. Louis, MO, Chicago, IL, and Bentonville, AR, our attorneys are centrally located and able to fly anywhere in the country to meet with a client face-to-face. This is unique amongst law firms. Many attorneys refuse to come to you, and will have "paralegals" or "support staff" screen calls and provide "advice." We think this is unconscionable. When you contact our office, you will speak to a lawyer immediately, free of charge. Call us toll-free for an immediate consultation. These are especially sensitive cases, and we handle them accordingly.

Gadolinium contrast MRI lawyers discuss nephrogenic systemic fibrosis claims

Schultz Legal Group — Tue, 08 Mar 2011 02:53:00 GMT

Litigation of the gadolinium based contrast agents is commencing in state and federal courts across the nation. Attorneys continue to file cases for injured patients suffering with the nephrogenic systemic fibrosis (NSF). The first case was filed in 2006, today there are over 400 lawsuits. Recently a case against GE Healthcare went to trial in United States District Court, in Northern Ohio.

Nephrogenic systemic fibrosis is a rare disorder, occurring in patients without a properly functioning kidney whom receive an injection of the gadolinium based contrast agent(dye) prior to an MRI. The disorder exhibits symptoms of fibrosis of organs and hardening of the skin. The only known cause of this disorder is the exposure to the gadolinium-based contrast agents. Unfortunately to present date, there is no known treatment or cure.

The FDA has mandated changes to the labeling on injection packaging, warning those with kidney conditions of the potential risks of receiving the contrast agent containing gadolinium. There are five gadolinium based contrast agents currently being manufactured by Bayer Healthcare Pharmaceuticals, Bracco Diagnostics Products, GE Healthcare and Tyco Healthcare. The contrast agents are known by the name-magnevist, prohance, multihance, omniscan and optimark. Two of the injection contrast agent manufacturing companies are settling cases and it is likely the others will soon follow.

If you have been exposed to gadolinium based MRI and contrast agents, contact the gadolinium exposure injury lawyers at Schultz & Myers be calling (866) 840-3636.

DuPuy hip implant defect claims - you may need a DePuy hip recall lawyer immediately

Schultz Legal Group — Wed, 02 Feb 2011 04:22:00 GMT

The failure rate of the DePuy hip implant system is approaching 15%, a figure that is down-right traumatic for patients who elected to have the Johnson & Johnson device surgically installed in their bodies. This rate of failure is the highest that our defective hip recall lawyers have seen in the past 15 years for any type of hip implant system. If you have a defective DePuy hip replacement system, you may be entitled to a cash settlement from Johnson & Johnson.

Patients who have the DePuy hip currently implanted in their body may require a revision surgery to remove the defective product and replace it with a hip implant from another manufacturer. Even if you are not experiencing current abnormal pain, it is wise to consult with your surgeon to find out whether the implant you have is one of the recalled lots. It is also important to contact a DePuy hip recall lawyer immediately to preserve the applicable statute of limitations in your case. The statute of limitations in these types of product liability cases against Johnson & Johnson will vary from state to state.

So what does it take to obtain a settlement or compensation for a DePuy hip recall injury claim? First, our lawyers must verify the make and serial number of your DePuy hip replacement. This is done by our lawyers requesting medical records from your surgeon. All of these costs are paid for by our law firm. In fact, if we determine that your DePuy hip is not part of the recall, you will owe us nothing for our costs and time expended investigating your case.

If a defective DePuy hip replacement is verified through our investigations, the next step for our attorneys is to put Johnson & Johnson on notice of a claim by filing a product liability lawsuit in Federal Court. This gets the ball rolling towards obtaining compensation for our clients. We take an aggressive approach in the handling of DePuy recall claims for compensation. This is the only way to go up against a large corporation such as J&J.

DePuy Hip Recall Lawyer - How to make a DePuy defective hip injury claim for compensation

Schultz Legal Group — Mon, 17 Jan 2011 02:06:00 GMT

As a DePuy hip recall lawyer, I can tell you that these cases for compensation are complex and involve theories of liability over and above the negligence found in an ordinary product liability lawsuit. Defective DePuy hip lawsuits are being filed at an alarming rate. Why? Because DePuy Orthopaedics ultimately put a hip implant system into the marketplace that has a reportedly 15% failure rate. That is unacceptable for the mass medical market. Patients with hip problems, whether they were caused by trauma or bone and ligament degeneration, need a safe solution.

With technologically driven surgical procedures, hip replacement procedures are no longer the intrusive undertakings they once were. With the right hip replacement device, a patient can be back on his or her feet in just a few weeks. However, when the hip replacement is defective, the patient can be left in a state far worse than even before the surgery. DePuy hip recall claims for compensation can result from a failure of the hip implant to perform as advertised. Premature failure of a DePuy hip implant can result in significant post-surgical pain and suffering, and the ultimate requirement for the patient to have a corrective surgery, also known as a "defective hip revision."

One of the first hurdles in a DePuy defective hip injury claim for compensation is the applicable statute of limitations in your state. Our DePuy hip recall injury lawyers are aggressive with these cases and file them immediately to preserve the time limits set for a product liability lawsuit on a state by state basis. Calling 1-866-840-3636 is the first step to preserving your right to file a DePuy defective hip lawsuit. Seeking a settlement for a hip recall claim will not result in fair compensation without the assistance of attorneys who are experienced in medical product litigation.

I need advice from a defective drug lawyer | drug recall attorney

Schultz Legal Group — Tue, 21 Dec 2010 23:50:00 GMT

Prescription medications are supposed to help patients cope with illness and sickness. So what happens when a defective drug causes injuries to the patient. These injuries can range from NSF to gall bladder infection to death. The injuries range from minor all the way to fatal. The problem the consumer has, is how to find out if there is a potential drug recall claim against the manufacturer. The best way to find this out is to contact a drug recall attorney immediately, before your time (statute of limitations), runs out.

So what can a defective drug lawyer do for you? First, he or she can file a personal injury claim against the manufacturer on behalf of the victim. This injury claim starts the process of preserving your stake in compensation for any damages you incurred from taking the medication. Second, a drug recall injury lawyer will research the applicable statute of limitation in your state. A statute of limitation is a time limit in which you are able to file your personal injury product liability claim against the manufacturer.

Medical product liability attorneys will also request all of your medical records and bills directly from your doctors. This is an important process of gathering the evidence necessary to win your case. The evidence required in a drug defect injury claim. Medical records and bills must be properly notarized from your medical providers in order to use them in court.

If you need more information, contact the drug recall injury lawyers at Schultz & Myers by calling our toll-free hotline at (866) 840-3636.

What makes a defective implant case or drug recall injury claim and what do I have to prove?

Schultz Legal Group — Thu, 02 Dec 2010 01:49:00 GMT

We receive calls every week from victims of negligent corporations who manufacture defective hip implants, defective devices, and recalled prescription medications. Patients and consumers depend upon these large corporations to act with a sense of prudency and corporate responsibility. So when it comes time to accountability for manufacturing and/or designing a defective product, why do they run for the protection of their high-priced lawyers. The reason is actually quite clear. Products liability claims can result in a snowball effect, one which can result in millions and millions of dollars in exposure to the corporation.

So what do you have to prove to win your defective hip implant or drug recall injury case? The elements vary for negligence based upon defective design, strict product liability, or manufacturing defect. A common misunderstanding is that just because a you are hurt by a product or drug, that there is automatically a case against the company. That is not the truth. You must prove that the company actually did something wrong, whereby anticipating the harm and knowledge of potential dangerous that were not disclosed to the consumer vis-a-vis an explicit warning or disclosure.

An important consideration to keep in mind when you think you may be the victim of a medical implant defect claim is to contact a personal injury attorney immediately to determine the applicable statute of limitation for your claim. This is absolutely critical. Why? Because if you do not obey the statute of limitation in your jurisdiction for your particular cause of action, then your claim could potentially become time-barred.

It is important to seek out the best legal representation for a defective hip implant or drug recall injury case. In doing so, you increase your chances at obtaining maximum compensation for your claim of injury.

Am I entitled to compensation for a defective hip or other defective medical device?

Schultz Legal Group — Wed, 20 Oct 2010 00:35:00 GMT

I have a DePuy hip implant and I don't know whether or not it is defective. Our defective hip implant lawyers hear this on a daily basis. Patients from across the country call our toll-free medical implant injury hotline each day wondering whether they are one of the thousands of people who will need a revision surgery to repair damage caused by a defective hip implant. Worried injury victims are wondering how they will cope with the added stress of mounting medical bills and future surgical costs, and if there is any way to be compensated for these losses.

Our national product liability lawyers investigate product defect claims and prosecute meritorious cases of injury resulting from use of a dangerous prescription drug, medical device, or medical implant. These types of cases require careful review of medical records and treatment history, which must be done by both our lawyers and staff medical doctors. Both legal and medical minds are needed to win any drug defective or defective hip implant claim. Lawyers alone are not enough to meet the legal burden of proof necessary to get results for injured clients.

Keywords: DePuy hip implant injury claim, DePuy hip replacement settlement compensation, DePuy hip implant lawyer

How do I know if I have a defective hip implant or defective hip replacement?

Schultz Legal Group — Wed, 13 Oct 2010 02:11:00 GMT

The past few years Stryker and Zimmer have both faced scrutiny by investigators regarding their hip implants. With Stryker and Zimmer, it was primarily an issue of audible squeaking noises. Patients could be heard walking down the hall of an office building due to a defect in the design of the Stryker hip implant system. Zimmer had a problem with its dorum cup hip implant system and it was later determined by authorities that the manufacturing plant of the dorum cup was using defective components. This resulted in recalls and countless revision surgeries.

Now the latest injustice is that being perpetrated by DePuy, a subsidiary of medical giant Johnson & Johnson. DePuy designs and manufactures the DePuy ASR hip implant system, which is intended to be a long term surgical orthopedic solution to patients in need of a hip replacement. The problem is that DePuy is recalling thousands and thousands of ASR hip implants due to a structural defect located in the acetabular cup. Patients with a DePuy ASR hip implant are urged to contact a DePuy hip implant recall lawyer immediately to discuss your rights.

The DePuy defective hip implant claim is thought to have effected almost 15% of all patients with this hip replacement system. A defect rate of this magnitude is a serious claim, enough so that the Federal Government is stepping in to investigate claims that DePuy had actual knowledge of the defect at a point in time in which the company could have made design changes, warned orthopedic surgeons of the defect, and warned patients of the known issues with the hip implant. This conduct arguably exceeds the threshold of negligence and reaches levels of recklessness that may entitle DePuy defective hip implant patients to make a claim for punitive damages.

You may be entitle to compensation for your defective hip implant claim. Contact our toll-free hip replacement defect lawyers by calling toll-free (866) 840-3636. Don't sit idly by in the hopes that your hip implant is not defective. Find out know before you have a potential statute of limitations issue with your product liability claim.

Reglan is a Dangerous Drug That Can Cause Tardive Dyskinesia and Users May be Entitled to a Reglan Compensation Claim

Schultz Legal Group — Wed, 15 Sep 2010 12:58:00 GMT

If you have been prescribed the drug Reglan, you need to take a step back and seek diagnosis from a doctor to rule out Tardive Dyskinesia. Reglan's link to Tardive Dyskinesia is being confirmed by our Reglan injury lawyers and we are filing Reglan compensation claims on behalf of our clients with TD. The symptoms of Tardive Dyskinesia are commonly known as facial grimacing and lip smacking, but can also include uncontrolled and unnecessary arm movements and leg movements. Generally the muscles begin to take on a mind of their own.

Tardive Dyskinesia has no known cure. What is known is that TD will cause serious problems in a victims life. Working and daily functions become difficult and a victim will find it hard to conceal the disorder from family, friends, and the general public. Reglan Tardive Dyskinesia claims for compensation will include past and future pain & suffering, lost wages, loss of earning capacity, emotional distress, and medical expenses for lost of treating the disorder.

If you have taken Reglan and are experiencing the side effects and symptoms of Tardive Dyskinesia, call a Reglan injury lawyer immediately to discuss your rights and claim for compensation. Don't wait until the statute of limitations expires and your Reglan claim is barred. Our Reglan recall injury lawyers will request your medical records from your doctors and work hard to prove your claim.

Link Established Between Accutane and Inflammatory Bowel Disease (IBD) Resulting in Accutane Claims for Compensation

Schultz Legal Group — Mon, 23 Aug 2010 00:55:00 GMT

Approximately 900 Accutane claims for compensation are now pending in multi-district litigation in New Jersey, with additional claims pending in Florida. After almost a decade of Accutane litigation between Roche and victims of the anti-acne drug, plaintiff's are now being compensated for developing inflammatory bowel disease (IBD) from taking this powerful acne medication. Accutane was originally approved by the FDA in 1982. In 2002, Accutane had become one of Roche's best-selling drugs, resulting in annual sales in excess of $200 million.

Isotretinoin is a synthetic molecule that happens to be an active ingredient found in Accutane. The FDA recently increased its requirements that all drug makers that include Isotretinoin in their products to warn customers about potential birth defects associated with even ONE SINGLE use of the drug by a pregnant woman. In addition to IBD and birth defects, Roche has come under fire for links to suicide and depression. Accutane injury victims are alleging that Roche failed to adequately warn of the potentially serious side effects associated with Accutane despite knowledge of the causal link between Accutane and various complications.

Our Accutane lawyers are using expert testimony, including opinions expressed by the American College of Gastroenterology to prove the link between Accutane use and inflammatory bowel disease. Recently, an Accutane plaintiff was awarded $25million dollars after proving that she developed IBD following use of Accutane.

If you would like to discuss an Accutane claim for compensation, contact a lawyer immediately by calling (866) 840-3636 for a case consultation and evaluation. Accutane cases still require numerous aspects of strict proof in order to be successful. Our Accutane litigation compensation attorneys investigate client's claims free of charge. We only recover attorneys fees if we win our clients case. Therefore, there is no financial risk for having our Accutane lawyers investigate your case.

Reglan Injury Lawyer / Reglan Drug Recall Lawyer Filing Reglan Injury Claims Against Manufacturer

Schultz Legal Group — Sat, 24 Jul 2010 02:02:00 GMT

Our Reglan injury lawyers are currently investigating hundreds of claims by Reglan users that this drug has caused serious and dangerous side effects. The most serious side effect, Tardive Dyskinesia (TD), is one claim we are investigating in particular. Tardive Dyskinesia caused by Reglan is an irreversible movement disorder that is commonly recognized by exhibiting the following symptoms:

Lip smacking
Facial grimacing
Involuntary movement of the cheek bones and mouth
Eye twitching
Involuntary arm and leg movements
Communication problems

The FDA recently issued the makers of Reglan a Black Box Warning, which is the highest warning issued to drug manufacturers. This particular warning was in regards to the direct link of Reglan use to Tardive Dyskinesia.

Users of Reglan are urged to contact our Reglan Injury Claim toll-free hotline at (866) 840-3636 to speak with a Reglan injury lawyer immediately. Our Reglan lawyers will file a Reglan compensation claim if you meet our standards for legal representation. Qualification is primarily based upon a review of your medical records, treatment, diagnosis and Relgan prescription history.

Our nationwide Reglan injury lawyers work on contingency fee, meaning there are absolutely no attorneys fees collected unless we win your case. Therefore, there will never be a charge to request and review a Reglan client's medical records, treatment, and diagnosis. If a potential Reglan user does not meet our legal standards for representation, there will be absolutely no attorneys' fees charged. Don't wait for your TD to get worse, contact a Reglan injury lawyer and file your Reglan settlement claim for compensation. TD is an irreversible, disturbing disorder that will affect almost every aspect of a Reglan user's life. Future quality of life is in question. Don't let this manfuacturer get off the hook.

Gadolinium Injury Lawyer is Filing Gadolinium MRI Contrast Injection Compensation Lawsuits

Schultz Legal Group — Tue, 29 Jun 2010 23:41:00 GMT

The side effects associated with Gadolinium exposure can be serious, life-threatening, and potentially fatal. One of the most serious side effects associated with Gadolinium exposure is Nephrogenic Systemic Fibrosis (NSF). This disorder is also known as Nephrogenic Fibrosing Dermopathy (NFD). These disorders can result in scaring of the skin and internal organs. Our nationwide Gadolinium Injury Lawyers are currently filing Gadolinium MRI Contrast Injection Compensation Lawsuits on behalf of innocent victims that are stricken with the serious side effects associated with these progressive disorders.

Gadolinium itself is used as a dye in magnetic resonance imaging (MRI) scans to produce a more detailed image of internal organs. Patients must be properly screened before being subjected to Gadolinium MRI contrast injections. Patients with existing kidney problems which are injected with Gadolinium are subject to NSF/NFD. Some of the symptoms of Gadolinium side effects include:

swelling of the legs
pain in the hips or pelvis
weakness and dizziness
thickening of the skin, including scale-like texture
skin burning sensations
impaired mobility and joint stiffness

If you have recently been exposed or injected with Gadolinium prior to MRI, contact a Gadolinium exposure injury lawyer immediately to see if you quality for compensation for your injuries. Nephrogenic Systemic Fibrosis and/or Nephrogenic Fibrosing Dermopathy are serious disorders that can become fatal. Seek the care of a specialist if you experience any of these symptoms and contact a Gadolinium side effect lawyer to discuss your rights.

Drug Recall Lawyer Discusses Defective Drug Claims and Dangerous Drug Claims

Schultz Legal Group — Sun, 13 Jun 2010 00:01:00 GMT

As a defective drug lawyer who handles defective drug injury claims, I know how victimized injury victims feel helpless at the hands of big pharmaceutical corporations. These large drug companies are well funded and defend injury claims now matter what the cost to the shareholders or victims themselves. When it comes time to fight these drug companies in court, our lawyers are aggressive and refuse to back down no matter how intimidating the battle may become. The great thing about courts of law are that they are the ultimate equalizer of power. Piers of the injury victims sit on a jury and are representative of the community. The jury has the power to change the future for the community and the country. A verdict against a major drug company makes a serious statement: We won't stand for corporate greed to wash out safety for the consumer.

Drug recall injury claims are complicated legal cases involving a battle of the experts. Physicians and chemists are often retained by both the plaintiff and the defendant to prove their case. These experts are an expensive but necessary component of each claim. After all, your case will never make it to the jury without proof of negligent or reckless conduct. The drug recall lawyer is not enough. It takes a small army of experts to convince a judge and jury that negligence did in fact take place.

Contact a drug recall lawyer at Schultz Legal Group if you suspect that a drug has caused you serious harm or injury. Our nationwide injury lawyers will investigate your drug recall claim by requesting medical records from your doctors and presenting them to our experts for review. Contact a nationwide drug recall lawyer by calling our drug recall injury claim hotline at (866) 840-3636. Don't be victimized twice.