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Cleft palate is a common birth defect in women who took Topomax during their pregnancy. According to research, the incidence of birth defects among women taking topiramate is higher than the birth defect rate in the rest of the population. Since half of pregnancies are unplanned, many women of childbearing age are on Topomax and not aware that they are pregnant. This could result in facial deformities, including cleft lip and cleft palate. While any birth defect is devastating and life altering a new cleft palate treatment has been approved that could help mothers and infants who have been injured by Topomax.

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According to reports, there are more than 4,000 cleft palate babies born every year in the United States. A new, non-invasive treatment may be available to treat these infants. Researchers indicate that the treatment is just as effective as the established method, but it is less invasive and expensive. Our birth defect attorneys in Boston are dedicated to advocating for victims whose lives have been altered by hazardous drugs. We are also abreast of developments in the medical community to help survivors of Topomax and other dangerous products.
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Knee and hip replacement surgeries continue to cause future complications for patients. Many of these complications related to defective medical devices and result in a necessary replacement. Whether you have already had a knee or hip implant or you need a replacement, you want to get the best medical treatment possible. The federal government has published a report calling attention to the best and worst hospitals for knee and hip replacement surgery.

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The government has identified 95 hospitals where patients were most likely to suffer setbacks and another 97 hospitals where patients had the most successful recoveries. The analysis is part of the government’s effort to strengthen the quality of care throughout the nation’s hospitals. Our medical malpractice attorneys in Massachusetts are dedicated to helping victims recover compensation for injuries caused by defective medical devices. We are also committed to enhancing medical safety for patients in Massachusetts and nationwide to prevent future injuries.
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Women who suffer from transvaginal mesh injuries may be embarrassed to discuss their condition with friends, loved ones, or even a medical professional. Victims may even postpone going to the doctor because they are waiting for symptoms to improve. However, if you or someone you love has suffered a transvaginal mesh injury, you know how severe the consequences can be. You also know that sustained injuries can significantly impact the quality of life for victims. Transvaginal mesh injuries are very severe and hundreds of thousands of women have suffered after having a vaginal mesh implant.

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Once considered awkward and personal problems, these injuries are now becoming increasingly common medical conditions for women who have had a vaginal mesh implant. Our transvaginal mesh injury attorneys are experienced in representing women who have suffered pain, complications, and dangerous injuries resulting from transvaginal mesh. For victims the consequences of a transvaginal mesh injury are not only painful and life-altering, they can also be deadly.
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Plaintiffs suffering from Topamax birth defects received good news when two recent cases resulted in combined compensation of $15 million for victims. In one of the two recent cases, the plaintiff was awarded almost $11 million in damages from Janssen Pharmaceuticals, the manufacturer of Topamax and a division of Johnson & Johnson. In the second case, $4.02 million was awarded to a family whose child was born with a cleft palate after his mother took Topamax while pregnant. magic-pills-1418156-m.jpg

The Topamax verdicts were a positive sign for plaintiffs because large verdicts for victims can sometimes make drug companies more eager to offer fair settlements to individuals whose defective drug cases are still pending. However, in this case, Janssen Pharmaceuticals does not appear to have given in yet to accepting that it is likely to be found liable for injuries in courts. Instead, Janssen Pharmaceuticals has announced the company’s intent to appeal the verdicts against it. Our Boston defective drug lawyers know that the outcome of the appeals could shape how future Topamax claims are resolved since a loss in appellate court could make Janssen much more likely to move forward with settlement talks.
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As the New Year approaches, many women currently suffering from transvaginal mesh complications will be closely watching the TVM litigation that is expected to occur in 2014. This year is likely to be an important one in which many TVM cases are resolved and in which the medical device manufacturers who sold TVM products may move forward with settling claims. nurseii-4-1158337-m.jpg

Ourtransvaginal mesh attorneys know that there are going to be many important milestones in TVM litigation in the upcoming year since there are several different bellwether trials that will occur. There are currently more than 40,000 lawsuits pending related to TVM products and each of these thousands of women could be affected by the outcome of trials beginning as early as January 10, 2014.
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Stryker Corp. is the manufacturer of hip replacement and resurfacing products including the Stryker Rejuvenate and the Stryker ABG II hip implants. The orthopaedic device company recalled both of these products in 2012 amid complaints that the devices had a high failure rate and that patients were suffering serious injuries as a result of product defects. hospital-room-449234-m.jpg

Unfortunately, before the Stryker products were recalled, our hip implant lawyers know that an estimated 20,000 Americans already had either a Rejuvenate or ABG II medical device used in their hip replacement procedure. Many of the patients who used these Stryker hip replacement devices have now begun to experience serious complications and, as a result, have filed lawsuits against the Michigan-based manufacturer. Several of these claims have now settled and many more cases could soon be resolved with plaintiffs being offered compensation out of court for their losses.
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Throughout the federal court system in the United States, there are currently more than 35,000 lawsuits pending related to complications associated with transvaginal mesh products. Transvaginal mesh, or TVM, was marketed as an alternative to traditional surgical procedures to treat pelvic organ prolapse (POP) or stress urinary incontinence (SUI). Unfortunately, thousands of women who had vaginal mesh surgically implanted began to experience erosion of the mesh, resulting in significant pain and serious complications, including perforation of the pelvic organs and recurrent POP. vitals-monitor-294066-m.jpg

Women who have experienced these side effects have filed lawsuits against vaginal mesh manufacturers seeking compensation for the tremendous losses they have faced. Those harmed by defective medical devices should be compensated for any medical costs that they incur to treat their injuries, such as surgical removal of the mesh. Individuals harmed by TVM products are also entitled to compensation for lost income, pain and suffering and emotional distress associated with injuries caused by the defective mesh products. Taking legal action to recover compensation for these losses is necessary, and the more than 35,000 lawsuits show that many women are exercising their legal rights.

When so many cases are filed by injured victims, Boston transvaginal mesh lawyers know that the formation of multi-district litigations is a common and effective way to resolve patient complaints. There are currently six MDLs pending and a group of plaintiffs is now calling for the creating of a seventh.
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Americans routinely suffer from cartilage damage, either from a single injury or because of age, requiring them to turn to dangerous alternatives, including Stryker knee replacements. Knee implants manufactured by Stryker have been linked to serious injury caused by the dangerous medical implants.
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According to reports,
researchers at UCLA have published the first study to track origin cells and the early development of articular cartilage. The research has led to a kind of “roadmap” for new treatments and therapies to repair cartilage damage caused by osteoarthritis. Advocates for the new therapy claim it can repair cartilage damage so that patients do not have to turn to dangerous medical devices, including Stryker products. Our Stryker hip attorneys are experienced in protecting victims and preventing future injuries. We are experienced in cases involving defective medical devices and can effectively protect your rights if you or someone you love has suffered medical malpractice as a result of a defective medical device.

Stryker has been the subject of litigation for injuries called by the defective knee replacements. In April 2013, a recall of the product was issued to prevent additional injuries caused by poorly-fitting, loose knee implants. The Stryker knee system is a brand developed by Stryker Orthopedics and approved by the FDA in 2005. Older models of knee implants used a single hinge, where the newer Stryker implant model pivoted to maintain a single radius design.
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Johnson & Johnson pharmaceuticals has been in the news recently, as the company’s subsidiaries have resolved pending claims against them… and not in the company’s favor. One subsidiary, Ethicon, may pay as much as $4 billion in damages to settle lawsuits from defective hip implants. Another, Janssen Pharmaceuticals, has had two multi-million jury verdicts against the company based on Topamax birth defects, and will be required to provide compensation of around $11 million to one family and just over $4 million to another. hands-1402625-m.jpg

For those who were taking Topamax during pregnancy and whose child was born with a birth injury such as a cleft palate, a heart or lung defect, a penile defect called hypospadias, malformed limbs or spina bifida, it is important to have claims evaluated to determine if you too have a legal right to damages. Our personal injury lawyers in Massachusetts can conduct case evaluations for families who may be affected by Topamax.
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As a patient, you trust that your doctor is well-informed of medical advancements, including developments and products that could be dangerous to your health. Patients who have been a victim of transvaginal mesh injuries may be surprised to discover that doctors were informed of the dangers in 2008. According to a public health notification published in 2008, there are serious complications associated with transvaginal placement of surgical mess to repair pelvic organ prolapse and to treat urinary incontinence.

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In an FDA warning issued on October 20, 2008, physicians were warned that complications associated with transvaginal mesh can have adverse effects and serious health consequences. Despite this initial warning and continued reports of injuries, the product has still not been recalled. Our medical malpractice attorneys in Massachusetts continue to advocate for the victims of Transvaginal Mesh injuries. We are dedicated to keeping our clients, the medical community, and patients aware of the dangerous of medical devices to protect future injuries.
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