Zimmer Holdings Inc, the designer of Zimmer Durum Hip Replacement Cup has announced a recall of their product. The Zimmer Durom Hip Replacement was designed to relieve patients suffering from non-inflammatory degenerative joint disease, which has now caused a series of complications and complaints from those patients. The cup is designed to bond securely to the patients hip socket. Unfortunately, in most patients the cup slipped out of place causing an immense amount of pain and suffering. Victims of the defective hip replacement endured several months to years with severe pain before undergoing a revisionary surgery to correct the displacement. The elderly, unaware of the problem were forced to undergo the stress and cost of a second surgery to alleviate their discomfort. These surgical procedures could have been avoided if the company investigated the problem sooner or conducted malfunction tests on their product.
In the spring of 2008, by order of the Food and Drug Administration, productions of the cups were eventually discontinued after an entire year passed being implanted in patients. Zimmer Holdings is taking responsibility for this problem, addressing the public's concerns regarding the defective hip replacement. Zimmer understands the pain and suffering their acetabular component caused in patients. Since their introduction in 2006, U.S. surgeons have completed successful surgeries while others have seen an increased rate in revisionary surgeries.
Hip replacement lawsuits are being filed against Zimmer Holdings, Inc nationwide. Zimmer Durom hip replacements are causing major complications and painful health conditions for patients who were implanted with this device. These side effects are not normal, as the hip replacement is meant to relieve pain and suffering, not worsen it. Contact a medical professional if you are experiencing such discomfort or pain.
Individuals harmed by the Zimmer Durom hip replacement surgery should seek legal help. The Long Island law firm of Rudolph F.X Migliore, P.C has the resources to handle product liability cases. The Migliore firm has represented clients in a wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful settlements for clients. If you or a loved one has experienced hip pain, limited mobility or suffering caused by the Zimmer Durom hip replacement surgery, contact the Long Island, NY Law firm of Rudolph F.X. Migliore, P.C at (631) 543-3663 to arrange a free case evaluation.
Visit: www.migliorelaw.com
Showing posts with label Product Liability. Show all posts
Showing posts with label Product Liability. Show all posts
May 10, 2011
April 15, 2011
Product Liability Law
Manufacturers, retailers and suppliers who distribute and sell products are solely responsible for the injuries their products may cause. Product liability pertains to a manufacturing defect, design or failure to warn the consumer of the products hazards. The U.S. Consumer Product Safety Commission works to ensure the safety of consumer products, while protecting the public from risk of serious injury or death. Unfortunately, in many cases dangerous products or defects with a product find their way into the marketplace every year.
Product Liability has three different categories: negligence, breach of warranty and strict liability. Strict liability makes a person legally responsible for the damage or loss caused by his or her actions. In tort law, strict liability is the imposition of the liability on a party without finding of fault. For example, an employer can be held liable for their employees or, most commonly, companies associate with defectively manufactured products. Additionally, strict liability also holds the manufacturer liable if the product is defective, even if the manufacturer was not negligent in making that product defective.
Fosamax and DePuy Hip replacements are examples of product liability cases. DePuy Hip Replacements are designed to replace worn or weakened parts of the body’s natural hip. Many implants are not fitting properly, due to poor design by the manufacturer, causing patients to feel pressure or experience pain. DePuy Orthopedics issued a global recall of its defective ASR Hip Resurfacing System and ASR XL Acetabular Systems. Those who have had one of the defective hip replacement systems implanted must now undergo a revisionary or second surgery due to pain, swelling and mobility issues. These additional surgeries cause extra pain and inconvenience to the patient, making DePuy liable.
Fosamax, the prescription drug to treat osteoporosis may now cause patients to face significant risk of hip/thigh/femur fractures. It was discovered that some patients using Fosamax had severe pain in joints, muscles and/or bones. Many of these patients who have suffered a broken femur, thigh or hip fracture after a minor fall from this medication do not have to be involved in an athletic activity for a fracture to occur. Victims of both Fosamax and DePuy Hip Replacements have had to seek medical attention due to the products malfunctions or defective functionality of the product.
While there are a multitude of products available on the marketplace, these products may sometimes harm the consumer. In this case there are may be companies that are liable. As with some defective medical products, the very medicines or products meant to improve patients’ lives actually cause harm or even death.
If you suffer serious injury from the use of a dangerous product, you have the right to pursue fair and complete compensation for medical expenses, pain, suffering and rehabilitation. For more information, please contact our office at 631-543-3663.
Product Liability has three different categories: negligence, breach of warranty and strict liability. Strict liability makes a person legally responsible for the damage or loss caused by his or her actions. In tort law, strict liability is the imposition of the liability on a party without finding of fault. For example, an employer can be held liable for their employees or, most commonly, companies associate with defectively manufactured products. Additionally, strict liability also holds the manufacturer liable if the product is defective, even if the manufacturer was not negligent in making that product defective.
Fosamax and DePuy Hip replacements are examples of product liability cases. DePuy Hip Replacements are designed to replace worn or weakened parts of the body’s natural hip. Many implants are not fitting properly, due to poor design by the manufacturer, causing patients to feel pressure or experience pain. DePuy Orthopedics issued a global recall of its defective ASR Hip Resurfacing System and ASR XL Acetabular Systems. Those who have had one of the defective hip replacement systems implanted must now undergo a revisionary or second surgery due to pain, swelling and mobility issues. These additional surgeries cause extra pain and inconvenience to the patient, making DePuy liable.
Fosamax, the prescription drug to treat osteoporosis may now cause patients to face significant risk of hip/thigh/femur fractures. It was discovered that some patients using Fosamax had severe pain in joints, muscles and/or bones. Many of these patients who have suffered a broken femur, thigh or hip fracture after a minor fall from this medication do not have to be involved in an athletic activity for a fracture to occur. Victims of both Fosamax and DePuy Hip Replacements have had to seek medical attention due to the products malfunctions or defective functionality of the product.
While there are a multitude of products available on the marketplace, these products may sometimes harm the consumer. In this case there are may be companies that are liable. As with some defective medical products, the very medicines or products meant to improve patients’ lives actually cause harm or even death.
If you suffer serious injury from the use of a dangerous product, you have the right to pursue fair and complete compensation for medical expenses, pain, suffering and rehabilitation. For more information, please contact our office at 631-543-3663.
March 8, 2011
Increase in Injuries with Medical Products
There has been much talk in the media about injuries from certain medical products. The two that have recently been problematic are the prescription drug Fosamax and certain DePuy hip replacements. Individuals must be aware of the impact that these medical products can have, both good and bad in order to make informed decisions. Recently, our firm has seen an increase in the amount of cases concerning Fosamax and DePuy hip replacements. At our firm, we have heard many victims tell their painful stories of their experiences with these products. We aim to keep our clients and the communities we serve aware of this information to protect their own health and well-being.
Fosamax is used to treat and prevent osteoporosis in post-menopausal women and steroid-induced osteoporosis in men. It has been determined that these patients who took the drug face significant risk of a spontaneous femur, hip and thigh fracture injury. Long Island Attorney Rudolph Migliore states, “Fosamax intended to relieve the suffering of arthritis but instead has had devastating and sometimes crippling results on people.” In FDA and independent studies, it was discovered that some patients using Fosamax had severe pain in joints, muscles and/or bones. Many of these patients have suffered a broken femur, thigh or hip fracture after a minor fall.
Fosamax is a type of drug categorized as a bisphosphonate. Bisphosphonates are a class of drug that strengthens bone density, usually used to treat osteoporosis. The FDA has concluded that although the drugs have not been proven to directly cause the fractures, the fractures are mainly reported to patients who have taken bisphosphonates. Based on this information, it has been reported that bisphosphonates cause multiple implications in the body including femur, hip and thigh fractures. The FDA has also encouraged healthcare professionals to re-evaluate their patients and determine whether bisphosphonate therapy is needed. Additionally, as of January 2011, there has been a link to an increased risk of osteonecrosis of the jaw. This condition hinders the patient from properly healing after minor traumas, surgery or tooth extractions. This leads to gum infections, jaw bone damage and loss of teeth. Fosamax should not be used for patients with certain disorders of the esophagus. Severe digestive reactions, heartburn, inflammation or ulceration of the esophagus may develop. For prescriptions starting this year, Fosamax will include a new label called a black box warning, updating the new information that has been uncovered about this drug. Fortunately, more patients will be aware of these side effects and will be able to take precautions to avoid injury. “Many products, either pharmaceutical or surgical are well intended but on occasion are not adequately investigated for potential side effects or effective functionality of the product. This is often done for financial or expedient considerations. When there are short cuts taken, people suffer,” says Mr. Migliore.
Another issue of concern in many different senior citizen communities has been the increase of patients needing multiple hip replacements because they were implanted with defective hip replacements, many manufactured by DePuy orthopedics. Some patients that were given the defective implant had to undergo revisionary surgery, making it a longer and harsher ordeal. The DePuy hip replacement is designed to replace worn or weakened parts of the body's natural hip. Studies have shown that one in eight patients will need a second procedure to correct the original implant. “A hip replacement is a difficult and painful procedure. To have additional pain and surgery as a result of a defective product is unimaginable,” states Rudolph Migliore. The implants are not fitting properly, due to poor design by the manufacturer, causing patients to feel pressure or experience pain. Unfortunately, in many cases when the device was removed, it left behind dangerous fragments. Complications include dislocation of the device, metal sensitivity and chronic pain or osteolysis, when fine bits of plastic debris wear off over time. These may cause other health complications and alter a patient’s quality of life. Often, even daily activities are affected by this hip replacement. If you are experiencing such discomfort, victim’s should seek help immediately from their doctor or medical professional. These side effects are not normal, as the hip replacement is meant to relieve pain and suffering, not add to it.
The Migliore law firm located on Long Island, has represented clients in a wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful verdicts. For more information or to set up a free consultation, contact Rudolph Migliore directly at 631-543-3663.
Rudolph F.X. Migliore, P.C.
Fosamax is used to treat and prevent osteoporosis in post-menopausal women and steroid-induced osteoporosis in men. It has been determined that these patients who took the drug face significant risk of a spontaneous femur, hip and thigh fracture injury. Long Island Attorney Rudolph Migliore states, “Fosamax intended to relieve the suffering of arthritis but instead has had devastating and sometimes crippling results on people.” In FDA and independent studies, it was discovered that some patients using Fosamax had severe pain in joints, muscles and/or bones. Many of these patients have suffered a broken femur, thigh or hip fracture after a minor fall.
Fosamax is a type of drug categorized as a bisphosphonate. Bisphosphonates are a class of drug that strengthens bone density, usually used to treat osteoporosis. The FDA has concluded that although the drugs have not been proven to directly cause the fractures, the fractures are mainly reported to patients who have taken bisphosphonates. Based on this information, it has been reported that bisphosphonates cause multiple implications in the body including femur, hip and thigh fractures. The FDA has also encouraged healthcare professionals to re-evaluate their patients and determine whether bisphosphonate therapy is needed. Additionally, as of January 2011, there has been a link to an increased risk of osteonecrosis of the jaw. This condition hinders the patient from properly healing after minor traumas, surgery or tooth extractions. This leads to gum infections, jaw bone damage and loss of teeth. Fosamax should not be used for patients with certain disorders of the esophagus. Severe digestive reactions, heartburn, inflammation or ulceration of the esophagus may develop. For prescriptions starting this year, Fosamax will include a new label called a black box warning, updating the new information that has been uncovered about this drug. Fortunately, more patients will be aware of these side effects and will be able to take precautions to avoid injury. “Many products, either pharmaceutical or surgical are well intended but on occasion are not adequately investigated for potential side effects or effective functionality of the product. This is often done for financial or expedient considerations. When there are short cuts taken, people suffer,” says Mr. Migliore.
Another issue of concern in many different senior citizen communities has been the increase of patients needing multiple hip replacements because they were implanted with defective hip replacements, many manufactured by DePuy orthopedics. Some patients that were given the defective implant had to undergo revisionary surgery, making it a longer and harsher ordeal. The DePuy hip replacement is designed to replace worn or weakened parts of the body's natural hip. Studies have shown that one in eight patients will need a second procedure to correct the original implant. “A hip replacement is a difficult and painful procedure. To have additional pain and surgery as a result of a defective product is unimaginable,” states Rudolph Migliore. The implants are not fitting properly, due to poor design by the manufacturer, causing patients to feel pressure or experience pain. Unfortunately, in many cases when the device was removed, it left behind dangerous fragments. Complications include dislocation of the device, metal sensitivity and chronic pain or osteolysis, when fine bits of plastic debris wear off over time. These may cause other health complications and alter a patient’s quality of life. Often, even daily activities are affected by this hip replacement. If you are experiencing such discomfort, victim’s should seek help immediately from their doctor or medical professional. These side effects are not normal, as the hip replacement is meant to relieve pain and suffering, not add to it.
The Migliore law firm located on Long Island, has represented clients in a wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful verdicts. For more information or to set up a free consultation, contact Rudolph Migliore directly at 631-543-3663.
Rudolph F.X. Migliore, P.C.
February 8, 2011
The Potential Side Effects of DePuy Hip Implants
DePuy Orthopedics, a division of Johnson and Johnson has issued a global recall of its orthopedic devices ASR Hip Resurfacing System and ASR XL Acetabular System in August 2010. These two defective hip replacements have already been implanted in patients for the past seven years since July 2003. Those who had one hip replacement system implanted must now undergo a revisionary or second surgery due to pain, swelling and mobility issues.
The DePuy hip replacement is designed to replace worn or weakened parts of the body's natural hip. Studies have shown that one in eight patients will need a second procedure to correct the original implant. The implants are not fitting properly, due to poor design by the manufacturer, causing patients to feel pressure or experience pain. The two recalled devices were available to patients since July 2003. Patients who had the product implanted over the last seven years may have received a defective DePuy hip replacement device.
Patients should contact their doctor to ensure they were not given the recalled device. Regardless of symptoms, DePuy recommends that patients seek medical attention even if you are not experiencing pain. There are several different models of hip implants and not all patients were given the defective product. Of those that were given the defective implant, only some of them need to have revisionary surgery. Medical professionals can diagnose patients and take the proper steps to avoid any dangerous complications that may occur.
Twelve percent of the DePuy hip replacement recipients have experienced hip pain, pain while walking, pain bearing weight, swelling and pain when rising from a seated position. Even daily activities are affected by this hip replacement. If you are experiencing such discomfort, victims should seek help immediately from their doctor or medical professional. These side effects are not normal, as the hip replacement is meant to relieve pain and suffering.
Unfortunately, in many cases when the device was removed, it can leave behind dangerous fragments that may or may not be discovered until years after. Complications include dislocation of the device, metal sensitivity and chronic pain or osteolysis, when fine bits of plastic debris wear off over time. These may cause other health complications and alter a patients quality of life.
Hip replacement lawsuits are being filed against DePuy nationwide. DePuy hip replacements are causing major complications and painful health conditions to victims. Individuals harmed by the DePuy hip replacement surgery should seek legal help. The Long Island law firm of Rudolph F.X Migliore, P.C has the resources to handle product liability cases. The Migliore firm has represented clients in a wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful settlements for clients.
If you or a loved one has experienced hip pain, limited mobility or suffering caused by the DePuy hip replacement surgery, contact the Long Island, NY Law firm of Rudolph F.X. Migliore, P.C at (631) 543-3663 to arrange a free case evaluation.
Visit: www.migliorelaw.com
The DePuy hip replacement is designed to replace worn or weakened parts of the body's natural hip. Studies have shown that one in eight patients will need a second procedure to correct the original implant. The implants are not fitting properly, due to poor design by the manufacturer, causing patients to feel pressure or experience pain. The two recalled devices were available to patients since July 2003. Patients who had the product implanted over the last seven years may have received a defective DePuy hip replacement device.
Patients should contact their doctor to ensure they were not given the recalled device. Regardless of symptoms, DePuy recommends that patients seek medical attention even if you are not experiencing pain. There are several different models of hip implants and not all patients were given the defective product. Of those that were given the defective implant, only some of them need to have revisionary surgery. Medical professionals can diagnose patients and take the proper steps to avoid any dangerous complications that may occur.
Twelve percent of the DePuy hip replacement recipients have experienced hip pain, pain while walking, pain bearing weight, swelling and pain when rising from a seated position. Even daily activities are affected by this hip replacement. If you are experiencing such discomfort, victims should seek help immediately from their doctor or medical professional. These side effects are not normal, as the hip replacement is meant to relieve pain and suffering.
Unfortunately, in many cases when the device was removed, it can leave behind dangerous fragments that may or may not be discovered until years after. Complications include dislocation of the device, metal sensitivity and chronic pain or osteolysis, when fine bits of plastic debris wear off over time. These may cause other health complications and alter a patients quality of life.
Hip replacement lawsuits are being filed against DePuy nationwide. DePuy hip replacements are causing major complications and painful health conditions to victims. Individuals harmed by the DePuy hip replacement surgery should seek legal help. The Long Island law firm of Rudolph F.X Migliore, P.C has the resources to handle product liability cases. The Migliore firm has represented clients in a wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful settlements for clients.
If you or a loved one has experienced hip pain, limited mobility or suffering caused by the DePuy hip replacement surgery, contact the Long Island, NY Law firm of Rudolph F.X. Migliore, P.C at (631) 543-3663 to arrange a free case evaluation.
Visit: www.migliorelaw.com
February 3, 2011
The Dangers of Fosamax, a Bisphosphonates drug
The Food and Drug Administration has continually reported the dangerous side effects of the prescription drug, Fosamax. Once known as the drug to treat and prevent osteoporosis in post-menopausal women and steroid-induced osteoporosis in men, it has been determined that these patients who took the drug face significant risk of a spontaneous femur fracture injury. Patients who suffer from this medication do not have to be involved in an athletic activity for a fracture to occur. In most cases, women and men have done basic daily activities and have experienced a fracture.
In recent news, the FDA has encouraged healthcare professionals to re-evaluate their patients and determine whether bisphosphonate therapy is needed. Bisphosphonates are a class of drugs that strengthen bone density, usually used to treat osteoporosis. The FDA has also concluded that although the drugs have not been proven to directly cause the fractures, the fractures are mainly reported to patients who took bisphosphonates. Based on this information, it has been reported that bisphosphonates cause multiple implications in the body other than femoral fractures.
As of January 2011, there has been a link to an increased risk of osteoporosis of the jaw. This condition keeps the patient from properly healing after minor traumas, surgery or tooth extractions, leading to loss of teeth, gum infections and jaw bone damage. Fosamax should not be used for patients with certain disorders of the esophagus. Severe digestive reactions, heartburn, inflammation or ulceration of the esophagus may be developed. For prescriptions starting this year, Fosamax will include a new label updating the new information that has been uncovered about this drug. More patients will be aware of these side effects and take whatever precautions are necessary to avoid injury.
Fortunately, patients may also ask their healthcare professional for any alternative remedies to reduce the skeletal disorder, osteoporosis. Maintaining a healthy lifestyle and a balanced diet, can significantly reduce the risk of bone less and may strengthen bone density. For patients suffering from osteoporosis, eating a healthy diet which includes adequate amounts of calcium and vitamin D are necessary, which can be found in green vegetables, dairy and some salt water fish.
Patients who experience pain in the groin or thigh area should seek medical attention immediately before a complete fracture occurs. For additional information, visit www.webmd.com
Fosamax is the link to many types of painful health conditions. Individuals harmed by Fosamax should seek legal help. The Long Island law firm of Rudolph F.X Migliore, P.C has the resources to handle Fosamax prescription drug cases. The Migliore firm has represented clients in a wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful settlements for clients.
If you or a loved one has used the osteoporosis medication Fosamax and later suffered a femur (hip/thigh/jaw) fracture contact the Long Island, NY Law firm of Rudolph F.X. Migliore, P.C at (631) 543-3663 to arrange a free case evaluation. Visit: www.migliorelaw.com
In recent news, the FDA has encouraged healthcare professionals to re-evaluate their patients and determine whether bisphosphonate therapy is needed. Bisphosphonates are a class of drugs that strengthen bone density, usually used to treat osteoporosis. The FDA has also concluded that although the drugs have not been proven to directly cause the fractures, the fractures are mainly reported to patients who took bisphosphonates. Based on this information, it has been reported that bisphosphonates cause multiple implications in the body other than femoral fractures.
As of January 2011, there has been a link to an increased risk of osteoporosis of the jaw. This condition keeps the patient from properly healing after minor traumas, surgery or tooth extractions, leading to loss of teeth, gum infections and jaw bone damage. Fosamax should not be used for patients with certain disorders of the esophagus. Severe digestive reactions, heartburn, inflammation or ulceration of the esophagus may be developed. For prescriptions starting this year, Fosamax will include a new label updating the new information that has been uncovered about this drug. More patients will be aware of these side effects and take whatever precautions are necessary to avoid injury.
Fortunately, patients may also ask their healthcare professional for any alternative remedies to reduce the skeletal disorder, osteoporosis. Maintaining a healthy lifestyle and a balanced diet, can significantly reduce the risk of bone less and may strengthen bone density. For patients suffering from osteoporosis, eating a healthy diet which includes adequate amounts of calcium and vitamin D are necessary, which can be found in green vegetables, dairy and some salt water fish.
Patients who experience pain in the groin or thigh area should seek medical attention immediately before a complete fracture occurs. For additional information, visit www.webmd.com
Fosamax is the link to many types of painful health conditions. Individuals harmed by Fosamax should seek legal help. The Long Island law firm of Rudolph F.X Migliore, P.C has the resources to handle Fosamax prescription drug cases. The Migliore firm has represented clients in a wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful settlements for clients.
If you or a loved one has used the osteoporosis medication Fosamax and later suffered a femur (hip/thigh/jaw) fracture contact the Long Island, NY Law firm of Rudolph F.X. Migliore, P.C at (631) 543-3663 to arrange a free case evaluation. Visit: www.migliorelaw.com
January 21, 2011
The Long-Term Effects of Asbestos Exposure
Asbestos exposure can lead to a number of deadly diseases and harmful conditions. Victims of asbestos exposure may experience asbestosis, a respiratory disease that leads to scar tissue forming in the lungs. The scar tissue prevents the lungs from freely exchanging gases and expanding and contracting properly. A doctor can make make a diagnosis of asbestos after running a series of test and consulting with a B-reader. A B-reader is a specially trained doctor who can read chest x-rays and make a determination of asbestosis.
Beyond asbestosis, exposure to asbestos can cause several other major diseases, including some rare forms not traditionally associated with asbestos. For instance, peritoneal mesothelioma is an asbestos-derived cancer that appears in the abdomen. Other patients may be diagnosed with pleural thickening where the asbestos scarring is spread out and defused throughout the lining of the lungs.
Mesothelioma is a lung cancer that is caused only by exposure to asbestos. It is a highly aggressive disease that is usually the result of prolonged exposure, and while there are ever-expanding treatment options, there is currently no cure.
Asbestos leaves behind a specific trail that can be conclusively linked to many types of asbestos exposure, pleural thickening and mesothelioma. This makes the manufacturers of asbestos products directly responsible for the destruction and suffering this product has caused. The courts have recognized this, making it possible for victims, and the families of victims, to recover compensation for their suffering.
If you or a loved one has been diagnosed with a type of asbestos or mesothelioma disease, call our offices at (631) 543-3663, for a free case evaluation. Our attorneys have handled over 1,200 asbestos cases and over 100 lung cancer cases.
Rudolph F.X Migliore, P.C.
Beyond asbestosis, exposure to asbestos can cause several other major diseases, including some rare forms not traditionally associated with asbestos. For instance, peritoneal mesothelioma is an asbestos-derived cancer that appears in the abdomen. Other patients may be diagnosed with pleural thickening where the asbestos scarring is spread out and defused throughout the lining of the lungs.
Mesothelioma is a lung cancer that is caused only by exposure to asbestos. It is a highly aggressive disease that is usually the result of prolonged exposure, and while there are ever-expanding treatment options, there is currently no cure.
Asbestos leaves behind a specific trail that can be conclusively linked to many types of asbestos exposure, pleural thickening and mesothelioma. This makes the manufacturers of asbestos products directly responsible for the destruction and suffering this product has caused. The courts have recognized this, making it possible for victims, and the families of victims, to recover compensation for their suffering.
If you or a loved one has been diagnosed with a type of asbestos or mesothelioma disease, call our offices at (631) 543-3663, for a free case evaluation. Our attorneys have handled over 1,200 asbestos cases and over 100 lung cancer cases.
Rudolph F.X Migliore, P.C.
December 11, 2010
Dangerous Prescription Drugs
Beware of Dangerous Prescription Drugs
"Modern medicine has done wonderful things to improve the quality of our lives. Yet horrible suffering results, when defective products or medications cause unintended consequences,” states Long Island attorney, Rudolph Migliore.
The Commack, NY law firm of Rudolph F. X. Migliore, P.C. has recently begun taking cases related to two dangerous prescription medications, Reglan and Fosamax.
Reglan (metoclopramide) - is a prescription drug that came on the market in generic form in 1982 and is also sold in the U.S. under generic names such as, Pylomid, Primperan, Gastrosil, Maxeran, Metlazel, Dibertil, Maxolon, Metoclopramide, Primperan, Plasil and other names. Doctors prescribe the drug to treat a variety of gastro-intestinal maladies, from acid reflux, nausea and vomiting due to surgery and cancer chemotherapy to gastroparesis.
Despite the many studies showing that Reglan was associated with a neurological disorder, tardive dyskinesia, the drug's manufacturers did not warn of it on the label until 2004 and did not add the Black Box warning until February 2009.
Tardive dyskinesia causes uncontrollable, repetitive movements of the body, such as grimacing, lip smacking, eye blinking or rapid leg and arm movements. The symptoms are rarely reversible and there is no known treatment.
Further investigation into Reglan has determined that patients, including infants and children, and the elderly, face significant risk of developing tardive dyskinesia. The risk is especially associated with those who have been on the drug for a long time, sometimes after a few dosages and even after the patient stopped taking the drug.
Fosamax – is used to treat and prevent osteoporosis in post-menopausal women, steroid-induced osteoporosis in men and other bone diseases. Investigation into Fosamax-related femur fractures determined that women and men who took the bisphosphonate drug face significant risk of a spontaneous femur fracture injury. These atypical hip/thigh fractures occur in minor or "low impact" falls from a standing height or less, as opposed to a traumatic accident or injury.
The FDA and other independent research studies indicate that femur fracture patients have reported experiencing severe pain of the joints, muscles and/or bones for periods of weeks to months before a complete fracture occurred.
Legal Help for Individuals Harmed by Defective Prescription Drugs
Extensive product liability experience gives the Long Island law firm of Rudolph F.X. Migliore, P. C. the expertise to handle complex defective prescription drug cases. The Migliore firm has represented clients in wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful settlements for clients.
If you or someone you care about has developed Reglan-induced tardive dyskinesia or who used the osteoporosis medication Fosamax and later suffered a femur (hip/thigh) fracture.
contact the Long Island, NY law firm of Rudolph F.X. Migliore, P.C. at (631) 543-3663 to arrange a free case evaluation. Visit: www.migliorelaw.com/
About Rudolph F.X. Migliore, P.C.
We are a civil and criminal law firm located on Long Island and offer legal services for victims of serious personal injury, including defective products, mesothelioma and medical malpractice. The firm’s practice extends to criminal defense, elder law and estate planning.
"Modern medicine has done wonderful things to improve the quality of our lives. Yet horrible suffering results, when defective products or medications cause unintended consequences,” states Long Island attorney, Rudolph Migliore.
The Commack, NY law firm of Rudolph F. X. Migliore, P.C. has recently begun taking cases related to two dangerous prescription medications, Reglan and Fosamax.
Reglan (metoclopramide) - is a prescription drug that came on the market in generic form in 1982 and is also sold in the U.S. under generic names such as, Pylomid, Primperan, Gastrosil, Maxeran, Metlazel, Dibertil, Maxolon, Metoclopramide, Primperan, Plasil and other names. Doctors prescribe the drug to treat a variety of gastro-intestinal maladies, from acid reflux, nausea and vomiting due to surgery and cancer chemotherapy to gastroparesis.
Despite the many studies showing that Reglan was associated with a neurological disorder, tardive dyskinesia, the drug's manufacturers did not warn of it on the label until 2004 and did not add the Black Box warning until February 2009.
Tardive dyskinesia causes uncontrollable, repetitive movements of the body, such as grimacing, lip smacking, eye blinking or rapid leg and arm movements. The symptoms are rarely reversible and there is no known treatment.
Further investigation into Reglan has determined that patients, including infants and children, and the elderly, face significant risk of developing tardive dyskinesia. The risk is especially associated with those who have been on the drug for a long time, sometimes after a few dosages and even after the patient stopped taking the drug.
Fosamax – is used to treat and prevent osteoporosis in post-menopausal women, steroid-induced osteoporosis in men and other bone diseases. Investigation into Fosamax-related femur fractures determined that women and men who took the bisphosphonate drug face significant risk of a spontaneous femur fracture injury. These atypical hip/thigh fractures occur in minor or "low impact" falls from a standing height or less, as opposed to a traumatic accident or injury.
The FDA and other independent research studies indicate that femur fracture patients have reported experiencing severe pain of the joints, muscles and/or bones for periods of weeks to months before a complete fracture occurred.
Legal Help for Individuals Harmed by Defective Prescription Drugs
Extensive product liability experience gives the Long Island law firm of Rudolph F.X. Migliore, P. C. the expertise to handle complex defective prescription drug cases. The Migliore firm has represented clients in wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful settlements for clients.
If you or someone you care about has developed Reglan-induced tardive dyskinesia or who used the osteoporosis medication Fosamax and later suffered a femur (hip/thigh) fracture.
contact the Long Island, NY law firm of Rudolph F.X. Migliore, P.C. at (631) 543-3663 to arrange a free case evaluation. Visit: www.migliorelaw.com/
About Rudolph F.X. Migliore, P.C.
We are a civil and criminal law firm located on Long Island and offer legal services for victims of serious personal injury, including defective products, mesothelioma and medical malpractice. The firm’s practice extends to criminal defense, elder law and estate planning.
December 7, 2010
Legal Help for Victims of Reglan-Induced Tardive Dyskinesia
Do a quick web search and you’ll find online forums where victims of tardive dyskinesia share heart-wrenching stories about how the prescription drug Reglan harmed them.
Available in generic form since 1982, Reglan is also sold in the U.S. under the brand name Maxolon and other names. Despite the many studies showing that Reglan was associated with tardive dyskinesia, the drug's manufacturers did place a warning on the label until 2004, and did not add the Black Box warning until February 2009.
Further investigation into Reglan determined that patients, including infants and children, and the elderly, faced significant risk of developing tardive dyskinesia. The risk is especially associated with those who have been on the drug for a long time, although symptoms have surfaced in patients after short-term use. Even after patients stop taking Reglan, symptoms of tardive dyskinesia occur.
For more than 30 years, doctors have been prescribing the drug Reglan to treat acid reflux, nausea, vomiting (in cancer patients) and gastroparesis, leaving countless victims to suffer from the frightening effects of tardive dykinesia.
A neurological disorder, tardive dyskinesia causes uncontrollable, repetitive movements of the body, such as grimacing, lip smacking, eye blinking or rapid leg and arm movements. The symptoms are rarely reversible and there is no known treatment.
If you or someone you care about has taken Reglan and developed symptoms of tardive dyskinesia, legal help is available. Call the Long Island, NY law firm of Rudolph F.X. Migliore, P.C. at (631) 543-3663 for a no cost, no obligation case evaluation.
While the harm the drug caused cannot be undone, attorney Rudolph Migliore and his team will fight to recover compensation for damages and hold liable parties responsible.
Extensive product liability experience gives the Long Island law firm of Rudolph F.X. Migliore, P. C. the expertise to handle complex defective prescription drug cases. The firm has represented clients in wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful settlements for clients and they can help you too. Visit: www.migliorelaw.com/
Available in generic form since 1982, Reglan is also sold in the U.S. under the brand name Maxolon and other names. Despite the many studies showing that Reglan was associated with tardive dyskinesia, the drug's manufacturers did place a warning on the label until 2004, and did not add the Black Box warning until February 2009.
Further investigation into Reglan determined that patients, including infants and children, and the elderly, faced significant risk of developing tardive dyskinesia. The risk is especially associated with those who have been on the drug for a long time, although symptoms have surfaced in patients after short-term use. Even after patients stop taking Reglan, symptoms of tardive dyskinesia occur.
For more than 30 years, doctors have been prescribing the drug Reglan to treat acid reflux, nausea, vomiting (in cancer patients) and gastroparesis, leaving countless victims to suffer from the frightening effects of tardive dykinesia.
A neurological disorder, tardive dyskinesia causes uncontrollable, repetitive movements of the body, such as grimacing, lip smacking, eye blinking or rapid leg and arm movements. The symptoms are rarely reversible and there is no known treatment.
If you or someone you care about has taken Reglan and developed symptoms of tardive dyskinesia, legal help is available. Call the Long Island, NY law firm of Rudolph F.X. Migliore, P.C. at (631) 543-3663 for a no cost, no obligation case evaluation.
While the harm the drug caused cannot be undone, attorney Rudolph Migliore and his team will fight to recover compensation for damages and hold liable parties responsible.
Extensive product liability experience gives the Long Island law firm of Rudolph F.X. Migliore, P. C. the expertise to handle complex defective prescription drug cases. The firm has represented clients in wide range of product liability cases in the last three decades and has worked with nationally recognized co-counsel to reach successful settlements for clients and they can help you too. Visit: www.migliorelaw.com/
September 22, 2010
Long Island Attorney Now Accepting Defective DePuy Hip Replacement Cases
FOR IMMEDIATE RELEASE
Long Island Attorney Now Accepting Defective DePuy Hip Replacement Cases
Commack, NY - September 20, 2010 - The Law Office of Rudolph F.X. Migliore, P.C. announced today the firm is now accepting cases involving defective DePuy hip replacements.
DePuy Orthopaedics issued a worldwide recall of its ASRTM XL Acetabular System and DePuy ASRTM Hip Resurfacing System used in hip replacement surgery due to the number of patients who required a revision surgery. Complaints to the Food and Drug Administration and DePuy studies showing that some patients experienced pain, swelling and mobility issues have led to revision surgery.
Within five years of initially receiving the product, approximately 12% of patients who received the ASRTM resurfacing device and 13% of patients who received the ASR total hip replacement needed corrective surgery. The revision surgery rate for the DePuy products is twice the industry average.
“Our attorneys recognize that people suffer a great deal of disability and pain as a result of defective products. Our goal is to protect their legal rights and interests as they seek to recover compensation for their injuries,” said lead attorney, Rudolph F.X. Migliore.
Decades of experience with difficult product liability cases gives attorney Rudolph F.X. Migliore exceptional know-how to handle defective product claims of every sort. Mr. Migliore’s law firm has also worked with nationally recognized co-counsel to reach settlements for clients. The firm has recovered compensation for over 1,200 victims of asbestos exposure, and is well positioned to represent clients in DePuy Hip Replacement cases.
For legal advice and guidance concerning defective DePuy Hip Replacement claims, please contact the Long Island, NY office of Rudolph F.X. Migliore, P.C. directly at (631) 543-3663.
Visit our website: www.migliorelaw.com/.
About the Law Firm of Rudolph F. X. Migliore, P.C. - Located on Long Island, the firm offers legal services for victims of asbestos, mesothelioma, lung cancer and other serious personal injuries. The firm also handles criminal defense, real estate and estate planning, and other legal matters.
Contact Person: Rudolph Migliore
Company Name: Law Firm of Rudolph F. X. Migliore, P.C.
Telephone Number: 631-543-3663
Web site address: http://www.migliorelaw.com/
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Long Island Attorney Now Accepting Defective DePuy Hip Replacement Cases
Commack, NY - September 20, 2010 - The Law Office of Rudolph F.X. Migliore, P.C. announced today the firm is now accepting cases involving defective DePuy hip replacements.
DePuy Orthopaedics issued a worldwide recall of its ASRTM XL Acetabular System and DePuy ASRTM Hip Resurfacing System used in hip replacement surgery due to the number of patients who required a revision surgery. Complaints to the Food and Drug Administration and DePuy studies showing that some patients experienced pain, swelling and mobility issues have led to revision surgery.
Within five years of initially receiving the product, approximately 12% of patients who received the ASRTM resurfacing device and 13% of patients who received the ASR total hip replacement needed corrective surgery. The revision surgery rate for the DePuy products is twice the industry average.
“Our attorneys recognize that people suffer a great deal of disability and pain as a result of defective products. Our goal is to protect their legal rights and interests as they seek to recover compensation for their injuries,” said lead attorney, Rudolph F.X. Migliore.
Decades of experience with difficult product liability cases gives attorney Rudolph F.X. Migliore exceptional know-how to handle defective product claims of every sort. Mr. Migliore’s law firm has also worked with nationally recognized co-counsel to reach settlements for clients. The firm has recovered compensation for over 1,200 victims of asbestos exposure, and is well positioned to represent clients in DePuy Hip Replacement cases.
For legal advice and guidance concerning defective DePuy Hip Replacement claims, please contact the Long Island, NY office of Rudolph F.X. Migliore, P.C. directly at (631) 543-3663.
Visit our website: www.migliorelaw.com/.
About the Law Firm of Rudolph F. X. Migliore, P.C. - Located on Long Island, the firm offers legal services for victims of asbestos, mesothelioma, lung cancer and other serious personal injuries. The firm also handles criminal defense, real estate and estate planning, and other legal matters.
Contact Person: Rudolph Migliore
Company Name: Law Firm of Rudolph F. X. Migliore, P.C.
Telephone Number: 631-543-3663
Web site address: http://www.migliorelaw.com/
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