Our Risperdal lawyers are accepting cases for unusual breast development in males.
Risperdal $70M Verdict In Philadelphia Risperdal Trial
Johnson & Johnson was hit with a $70 million verdict on Friday when a Philadelphia jury found that the antipsychotic drug Risperdal had caused an adolescent boy to grow female breasts.
Risperdal and Enlarged Breasts In Young Males
Risperdal has been linked to enlarged breasts in your males. This is a condition called gynecomastia. he Growth of male breasts can cause severe emotional distress. Surgery may be required to correct the condition. Risperdal may increase levels of prolactin, a hormone which stimulates breast development in women. Young boys who have taken prolactin and are displaying increased levels of this hormone may develop male breasts or gynecomastia.
Can I Join The Risperdal Gynecomastia Lawsuits?
If you are a male and have enlarged female breast call no to see if you qualify to join others in a Risperdal lawsuit. Risperdal is the brand name for the drug called Risperidone. This is approved to treat schizophrenia and bipolar disorders. Risperdal but has resulted in gynecomastia. Gynecomastia, the development of real female breasts. It is real breast tissue growth caused by an increase in the hormone prolactin. If you have enlarged breasts with; Pain, Swelling, Tenderness and Nipple discharge and may
need surgery to remove excess breast tissue you may be able to join the Risperdal class action lawsuits.
Get A Risperdal Lawyer
Lawsuits are being filed against Johnson & Johnson through its subsidiary Janssen Pharmaceuticals, for failing to properly inform doctors and patients about the effects of Risperdal.
If you have kidney failure after taking Nexium or Prilosec contact our Nexium- Prilosec Lawsuit Helpline.
If you have a diagnosis of kidney disease and proof that you were taking Nexium, Prilosec or other acid reflux- proton-pump inhibitor medications for extending periods we can help. Lawsuits are being filed by our Nexium- Prilosec Kidney Disease lawyers.
Proton Pump Inhibitor Lawsuits Filed
Nexium, Aciphex, Protonix, Prevacid, Zegerid,omeprazole, Dexilant, Prilosec, omeprazole
Kidney Side Effects of Proton Pump Inhibitor drugs:
Kidney Failure Lawyer
Chronic Kidney Failure,
Acute Kidney Failure,
Acute Interstitial Nephritis,
Dialysis Treatment, and
Kidney Removal or Transplant Surgery
Symptoms Of Kidney Disease:
Nausea and vomiting, Passing only small amounts of urine, Swelling, particularly of the ankles, and puffiness around the eyes, Unpleasant taste in the mouth and urine-like odor to the breath,
Persistent fatigue or shortness of breath, Loss of appetite,Increasingly higher blood pressure, Muscle cramps, especially in the legs, and Pale skin, Excessively dry, itchy skin.
Get a Nexium or Prilosec Helpline lawyer
Our extensive bleeding blood thinner lawyers are accepting Eliquis and Xarelto cases for extenive bleeding injury and wrongful death claims.
Eliquis is a blood thinner that is similar to Pradaxa, and Xarelto. The problem appears to be once bleeding begins it is very difficult to control. This can result in severe internal bleeding and bleeding that results in fatal injury.
Eliquis Injury Lawsuits Filed For:
Wrongful Death from extensive bleeding
There is currently no reversal agent for Eliquis internal bleeding.
If you have lost a loved one due to extensive bleeding from Eliquis contact our Blood thinner class action lawsuit department today
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,
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
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.