Do You Want To File A Talcum Powder Lawsuit?
If you have used talcum powder or baby powder products and developed ovarian cancer you may be able to file a Talcum Powder lawsuit Current lawsuits Johnson & Johnson claim that long-term use of talc-based products caused women to develop ovarian cancer. Victims claim that they were not warned of the risks associated with these talc products. Women and their families may be able to seek compensation for ovarian cancer diagnosis with the help of one of our lawyers.
Is There A Risk of Talcum Powder Causing Ovarian Cancer?
Talcum powder lawsuits claim Talcum Powder caused ovarian cancer. When used as a feminine hygiene product, talc particles can travel through the vagina and into the ovaries and remain trapped for years. These talc particles can cause inflammation and eventually lead to the growth of ovarian cancer cells.
Studies Claim Dangers Of Talcum Powder
Although Johnson & Johnson maintains that talcum powder is safe for use, plaintiffs in ovarian cancer lawsuits offer studies that suggest an association between talc and ovarian cancer dating as far back as 1971. In 1994, Johnson & Johnson was put on notice of a link between talc and ovarian cancer. A letter was sent from the Cancer Prevention Coalition to the then-CEO of the company.
Will There Be a Talcum Powder Ovarian Cancer Class Action Lawsuit I Can Join ?
According to news reports, more than 1,200 women claim talcum powder caused their ovarian cancer. Currently the lawsuits are being filed at the state level.
Talcum Powder Lawsuit Settlements
A $72 million talcum powder verdict is handed down against Johnson & Johnson in favor of a woman who claimed that long-term Shower-to-Shower use for feminine hygiene caused her to develop ovarian cancer. The verdict included a $62 million award of punitive damages against the company.
Our talcum powder cancer lawyers are available to discuss your options.
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
Xarelto Lawsuit Attorney Helpline
Xarelto is an anticoagulant prescribed to prevent blood clots in patients suffering from atrial fibrillation, deep vein thrombosis, pulmonary embolisms, or stroke.It is also prescribed for patients who have undergone a knee or hip replacement surgery to avoid clotting. The Xarelto Helpline is concerned about seniors prescribed Xarelto.
Bayer and Johnson & Johnson’s Janssen Pharmaceuticals are the manufacturers of Xarelto. Lawsuits claim these manufacturers’ neglected to warn patients of Xarelto side effects. Our Xarelto lawyers are accepting Xarelto lawsuits for extensive bleeding side effects from Xarelto.
The Xarelto Helpline
is helping victims of Xarelto connect with an Xarelto lawyer.
Xarelto lawsuits are being filed for Xarelto bleeding victims:
Xarelto internal bleeding lawsuits,
Xarelto hemorrhagic stroke lawsuits,
Xarelto gastrointestinal bleeding lawsuits,
Xarelto brain bleed lawsuits,
Xarelto death due to irreversible bleeding
Get An Xarelto Lawyer
If you, a loved one or someone you care for has been injured by using the anti-coagulant drug Xarelto, it is imperative that you speak to an Xarelto attorney. Speak to one of our Xarelto lawyers today for your free case consultation.
Xarelto Extensive Bleeding Lawyers For:
- Death caused by uncontrolled bleeding
- Intestinal bleeding
- Brain hemorrhage
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
IVC Filter Lawyers Advise – Bard IVC Filter Lawsuits Consolidated
Bard IVC Filter lawsuits have been transferred to a federal court in Arizona.
IVC Filter lawyers of Class Action Lawyer Network will help victims injured by the defective IVC filters.
IVC Filter MDL
A transfer order filed Monday, in the U.S. Judicial Panel on Multidistrict Litigation (JPML), resulted in all present and future federal product liability lawsuits against inferior vena cava filter (IVC filter) manufacturers, C.R. Bard, Inc. and Bard Peripheral Vascular, Inc. (BPV), to be centralized in a multidistrict litigation (MDL) in the District of Arizona.
What Are IVC Filters?
IVC filters are surgical implants that catch blood clots before they travel to the lungs to avoid causing a pulmonary embolism. The Bard IVC Filter devices are fracturing, tilting, migrating, or puncturing the vena cava.
FDA Vena Cava Filter Warnings
The U.S. Food and Drug Administration issued a safety warning in 2010, citing that more than 900 IVC Filter adverse event reports were filed over five years
A study published in the April 2013 edition of Jama Internal Medicine, found that less than 10% of retrievable IVC filters surveyed were successfully removed. They also reported that 8% of persons surveyed still suffered venous thrombotic events while the IVC filter was in place.
In 2014, the FDA issued an updated warning to doctors recommending that IVC filters be removed within one to two months once the need for the filter has passed. They noted that doctors may not have previously been made aware of the urgency surrounding retrieval of the device.
IVC Filter Lawyers
IVC filter lawyers will help you get compensation as part of the Bard IVC filter MDL, which has been consolidated to the U.S. District Court of Arizona.
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.