The hip and knee lawsuit attorneys at Class Action Lawyer Network are accepting:
Faulty Hip Replacement Lawsuits for :
- DuPuy ASR,
- Zimmer MMC,
- DePuy Pinnacle (metal on metal),
- Wright Medical Conserv,
- Stryker Rejeuvenate or ABG11,
- Stryker Accolade/Citation/ Meridian,
- Encore Metal on Metal
Faulty Knee Replacement Lawsuits For :
Zimmer Persona Knee
Knee Implant Failure Complications: dislocation, early joint breakdown due to poor design infection, and loosening at the knee joint,
Taxotere Baldness Lawyers For Permanent Hair Loss Lawsuits
Have you received Taxotere for breast cancer?
Taxotere can result in hair loss or baldness that is permanent.
Taxotere is a chemotherapy drug used for the treatment of breast cancer. Taxotere has been shown to cause permanent hair loss. Taxotere lawyers are filing permanent hair loss lawsuits against the manufacturer of Taxotere, Sanofi-Aventis. The U.S. Food and Drug Administration has acknowledge that Taxotere can result in permanent hair loss, and this warning will now be placed on the Taxotere label.
If you or a loved one has been a victim of permanent hair loss from Taxotere contact a Taxotere class action lawyer today
Power Morcellator Lawyers Filing Lawsuits
Power Morcellator Device Spreads Uterine Cancer Continue To Grow
Morcellator lawyers advise that power Morcellator lawsuits have been consolidated by the Judicial Panel on Multidistrict Litigation. 2652 cases have been filed for women who underwent laparoscopic power morcellation for hysterectomies or myomectomies and were put at risk for spreading previously hidden cancer cells.
- The Morcellator has jaw-like blades that rapidly spin to shred fibroid tissue so that the pieces are able to be removed from the body.
- It is now known that as tool does this, it uncovers and disseminates uterine sarcoma cells.
- The FDA issued a safety warning against laparoscopic power morcellation procedures due to the risk of spreading cancer.
- Many women have developed serious or fatal leiomyosarcoma.
- There have been deaths of “hundreds, if not thousands of women in America”.
Morcellator lawyers at Class Action Lawyer Netowork are accepting cases for women who have undergone power morcellation and who has subsequently been diagnosed with cancer.
Invokana lawyers are filing Invokana lawsuits for Ketoacidosis, heart attack, diabetic coma and deaths.
Invokana is an SGLT2 inhibitor that may lead to ketoacidosis. The FDA has issued warnings that
Have been shown to cause serious medical conditions including:
The Invokana lawyers at Class Action Lawyer Network are filing lawsuits on behalf of patients who suffered serious injuries after taking:
Xigduo XR (dapagliflozin/metformin)
The FDA Issued A Warning For Invokana
In May 2015, the FDA warned that Invokana may put patients at risk for ketoacidosis. Ketoacidosis may cause diabetic comas or death.
The Dangers Of Invokana Resulting In Lawsuits
Our Invokana lawyers are filing lawsuits claiming the manufacturer failed to warn patients and doctors of the risks of kidney failure, myocardial infarction, and ketoacidosis Invokana os a medication given to diabetics to help lower blood sugar.
Invokana Class Action Lawyers
Our Invokana lawyers are filing Invokana lawsuits for kidney damage,heart attacks, and ketoacidosis complications from the medication Invokana. Lawsuits are being filed because the manufacturers and of SGLT2 inhibitors (such as Johnson & Johnson, Janssen Pharmaceuticals Inc., AstraZeneca & Boehringer Ingelheim) failed to warn patients and physicians of the risks of kidney failure, myocardial infarction and ketoacidosis.
What is Invokana?
You may have been prescribed Invokana to improve glycemic control and lower blood sugar if you are a type 2 diabetic. These medications lower a person’s blood sugar by causing the kidneys to remove it through the urine.
Heart Attack Ketoacidosis Drugs
Canagliflozin and Metformin,
Dapagliflozin and Metformin extended-release,
Empagliflozin and Linagliptin.
Risks Alert For Kidney Failure
Kidney failure occurs when your kidneys stop functioning. When your kidneys stop properly functioning, you will experience cause weakness, shortness of breath, lethargy, confusion, abnormal heart rhythms and even sudden death.
Risk Alert For Heart Attacks
A heart attack results in the death of cells within the heart. This is caused by a restriction of blood. It occurs when there is a blockage in the arteries preventing blood from reaching portions the heart.
Risk Alert For Ketoacidosis
Ketoacidosis is high levels of ketones. Ketoacidosis can result in a patient suffering a diabetic coma, extended hospitalization and even death. The FDA warns that SGLT2 inhibitors for diabetes may result in a serious condition of too much acid in the blood. Medications in the class include AstraZeneca’s Farxiga and Xigduo, Jardiance and Glyxambi from Lilly and Boehringer Ingelheim. J&J also combines the active ingredient in Invokana with metformin and markets it as Invokamet.
Speak to one of our Invokana lawyers today
Class Action Lawyer Network lawyers are now accepting
Benicar Gastrointestinal Damage Lawsuits
Bard Blood Clot Vena Cava Fracture Lawsuits
Zocar Kidney Failure Lawsuits
Xarelto Extensive Bleeding Lawsuits
GranuFlo Dialysis Medication- Immediate Heart Attack Lawsuits
The lawyers of Class Action Lawyer Network are always up to date on all the current drugs and devices harming patients or with knew FDA warnings.
What Is Benicar? What Is The Benicar Lawsuit?
Benicar is a blood-pressure medication that has been linked to gastrointestinal injury including sprue-like enteropathy. This disease causes chronic diarrhea and weight-loss. The lining of the intestine is no longer able to absorb nutrients due to the lining damage from this medication. Benicar lawsuits have been filed for people with this severe side effect.
What Is The Bard Vena Cava? What Is The Bard Vena Cava Lawsuit?
The Bard IVC filters are designed to capture blood clots before they enter the lungs. These filters have fractured and fragments have migrated puncturing internal organs and veins.
Surgeons have implanted the inferior vena cava filter in the veins of patients to prevent blood clots from moving into the lungs. The filters capture the clots in the blood stream. Reported adverse incident complications include punctured organs, blood vessels and filter migration to different parts of the body.
IVC Filter Lawsuits Filed
The Bard Recovery filter
The Bard G2 filter
The Bard G2 Express filter
What Is Zocar? What Are The Zocar Lawsuits For?
Zocor is a cholesterol drug and is prescribed to many people with high cholesterol. Zocar has warnings for Zocor liver damage and muscle damage. Lawsuits are being filed for liver damage and liver damage death from Zocar
What Is Xarelto? What Are The Xarelto Lawsuits For?
Xarelto (rivaroxoaban) is an anticoagulant prescribed to reduce the risk of stroke, deep vein thrombosis (DVT), pulmonary embolism (PE) and blood clots. injuries. It is prescribed to people with non-valvular atrial fibrillation and following knee and hip replacement surgery to prevent blood clots.
Xarelto Extensive Bleeding Lawsuits Are Being Filed For:
Gastrointestinal bleeding- bleeding ulcers,
Brain Hemorrhage and Deaths
What Is GranuFlo?
Granuflo dry concentrate and NaturaLyte liquid concentrate are among the most widely used products during hemodialysis treatment.
What Are GranuFlo Dialysis Medication Lawsuits Filed For?
Sudden MI or heart attack
Class Action Benicar lawyers announce a new Benicar lawsuit helpline because the number of Benicar lawsuits in the multidistrict litigation, as of July 15, 2015, has reached 915 lawsuits. The lawsuits are against the makers of Benicar, Daiichi Sankyo, Inc., its parent company, Daiichi Sankyo Co. Ltd., and Forest Laboratories Inc. Benicar is a drug prescribed to patients with high blood pressure and has been noted to cause the development of sprue-like enteropathy. This is a severe gastrointestinal condition with symptoms such as chronic diarrhea, nausea and vomiting, and significant weight loss and malnutrition.
Benicar was approved by the FDA in April 2002. In July 2013 the FDA issued a Safety Warning for Benicar after reviewing data submitted by the Mayo Clinic. The data showed that Benicar may be associated with sprue-like enteropathy. The first lawsuits against Daiichi Sankyo were filed soon after the FDA issued the warning. This multidistrict litigation, formed in April 2015, is based in the US District Court in New Jersey.
Benicar lawyer are interested in representing individuals with these symptoms as the result of taking Benicar.
For more information on Benicar, or if you believe you have been injured by using Benicar, speak to one of our qualified Benicar attorneys.
Benicar Gastrointestinal Injury Lawyers
Filing Benicar Intestinal Injury Lawsuits
What Is Benicar?
Benicar is a high blood pressure medication. Benicor has been linked to severe intestinal injury, intestinal damage, chronic diarrhea, malnourishment and severe weight loss. Seniors are the largest population receiving prescriptions for Benicar and are the most vulnerable to sever injury from Benicar.
FDA Benicar Warnings
The FDA has warned patients and doctors that Benicar (olmesartan medoxomil) may cause a severe gastrointestinal (GI) problem called Villous Atrophy. Benicar causes the intestines to lose the texture and makes it difficult to absorb nutrients. This leads to malnutrition which and other digestive problems. This is very dangerous for seniors and can lead to death or hospitalization because of dehydration, chronic diarrhea and malnutrition. Villous Atrophy can result in limiting the ability of the small intestines to absorb nutrients from food. At the most serious stages, villous atrophy causes damage to the intestinal crypts, which is the intestinal lining that surround the villi.
Benicar Villous Atrophy Lawyers Filing Benicar Lawsuits
Benicar has been used by millions of people. Benicar warnings did not adequately disclose how serious the side effects form this medication is.
The Benicar lawyers at Class Action Lawyer Network are filing claims for individuals who have experienced chronic diarrhea, sprue-like enteropathy or villous atrophy after using Benicar.
Hemorrhages Caused by Xarelto
Xarelto Lawyers Filing Extensive Bleeding Lawsuits
Our Xarelto lawyers are accepting Xarelto lawsuits for hemorrhage caused by Xarelto. Nationwide Xarelto attorneys are reviewing cases of excessive bleeding from Xarelto. In a recent Xareleto lawsuit a widow from Missouri has filed an Xarelto claim against Johnson & Johnson, Janssen Research & Development, Bayer Healthcare Pharmaceuticals, et al. to demand that the defendants be held liable for the death of her husband. Dixie A. Smith, surviving spouse of Jay Christopher Smith, filed the complaint in the U.S. District Court for the Eastern District of Louisiana, where it joins similar lawsuits pending in multidistrict litigation (MDL) No. 2592 before Judge Fallon.
The plaintiff contends that had her late husband never taken the defendants’ medication, Xarelto, he would not have suffered a deadly intracerebral hemorrhage. Ms. Smith is suing for compensatory damages for past, present, and future economic expenditures incurred as a result of the decedent’s use of Xarelto, including medical and funeral expenses, loss of earnings, loss of companionship and support, and loss of the prospective net accumulations of an estate.
Xarelto Caused A Brain Hemorrhage
The decedent’s physician prescribed Xarelto (rivaroxaban) during December of 2012. He continued to take the medication as prescribed until May of 2013. On May 4, the decedent was admitted to an intensive care unit (ICU), at which point the hospital staff discontinued his use of Xarelto. He was transferred to the care of a specialty hospital unit on May 18 and on May 22 he died of the intracerebral hemorrhage.
According to Ms. Smith’s Xarelto lawsuit, her late husband’s passing was a direct result of his use of rivaroxaban, which he reportedly never would have taken had he been fully informed of the risks. Xarelto is an anticoagulant or blood thinner that is prescribed for the treatment and prevention of blood clots. The medication is intended to reduce the risk of life-threatening complications caused by blood clots, including pulmonary embolism and stroke.
The product liability lawsuit regarding Xarelto draws attention to several reviews and clinical studies of the drug, including a 2012 report issued by The Institute for Safe Medication Practices. This report stated that there had been “356 reports of serious, disabling, or fatal injury in which rivaroxaban was the primary suspect drug. The report more than doubled from the previous quarter total of 128 cases.”
The organization brought these statistics to the attention of the defendants, who reportedly advised The Institute for Safe Medication Practices that the data did not reflect any safety issues that required action. Ms. Smith’s Xarelto lawsuit alleges that the defendants prioritized profit over patient safety.
Her complaint further claims that the defendants concealed their knowledge of the severe and life-threatening complications of Xarelto from consumers and the medical community. The lawsuit notes that the pharmaceutical giants failed to highlight the risks of uncontrollable bleeding events, nor did they provide medical protocols for stabilizing patients suffering from these bleeding events.
Xarelto had been marketed as a replacement for an older blood thinner, warfarin (Coumadin). Warfarin has been used for years for patients who may be at a higher risk of blood clots. However, patients taking warfarin required regular medical monitoring and dietary restrictions, which Xarelto had promised to eliminate.
Our Xarelto lawyers have been reviewing claims for excessive bleeding like these. Xarelto lawsuits are now consolidated in an MDL because many people have suffered injuries of a same type from Xarelto. Speak to an Xarelto lawyer today.
Lawyers Filing Ovarian Cancer Lawsuits For Baby Powder
Talcum Powder Ovarian Cancer Lawsuits
Do You Want To File A Baby Powder Cancer Lawsuit?
Studies show that talcum-based powder can cause ovarian cancer in women who have used it for genital/perineal hygiene. Studies dating back to 1982 have consistently linked prolonged talc-based baby and body powder usage with ovarian cancer. The talc particles moves through the female reproductive system and settles in the ovaries. These particles may remain in the ovaries for many years, creating inflammation resulting in the development and proliferation of cancer cells.
Studies HAVE Linked Ovarian Cancer to Talc-Based Baby/Body Powder
The pathology reports and tissue samples that were used to diagnose the ovarian cancer can now be examined to determine whether your ovarian tissues contain talc particles. Talc particles can be found in the pelvic lymph nodes, ovaries, and fallopian tubes and take many years to disintegrate and exit the body. The talcum powder cancer lawyers at Class Action Lawyer Network are speaking to women about talc having caused your ovarian cancer.
Speak To A Talcum Powder Lawyer
If you have been diagnosed with ovarian cancer after long term use of talcum-based products, such as Johnson & Johnson Baby Powder, Shower to Shower, and others we want to talk to you regarding filing a talcum powder cancer lawsuit.