Logan

GranuFlo Lawyers, NaturaLyte Lawsuits

Fresenius Medical is the manufacturer of GranuFlo and NaturaLyte acid concentrate. These are drugs used in dialysis treatment. There has been a recall of these dialysis drugs and lawsuits are being filed.

Injury and death has resulted from these drugs:

  • GranuFlo cardiovascular death,
  • GranuFlo sudden cardiac death,
  • GranuFlo cardiopulmonary arrest,
  • GranuFlo heart attack,
  • GranuFlo catastrophic cardiovascular injuries

Fresenius manufactures GranuFlo and NaturaLyte used in dialysis. These drugs cause alkalosis, a condition associated with an increase in cardiovascular fatalities.

The FDA received complaints describing alkali dosing errors that occurred during hemodialysis using dialysate concentrates containing acetic acid and acetate. When metabolized, these potential sources of alkali can contribute to elevated bicarbonate levels in patients undergoing hemodialysis.

This can contribute to metabolic alkalosis, which is a significant risk factor associated with :

Low blood pressure

Cardiopulmonary arrest

Cardiac arrhythmia

Sudden heart attack

Stroke

Hemodialysis cardiopulmonary arrest

A study which was conducted between January and December of 2010 found that patients with pre-dialysis bicarbonate levels greater than 28mEq/L were 4.7 times more likely to suffer a cardiac arrest. The study also discovered that patients with pre-dialysis potassium lower than 4 mEq/L had a 6.3 times higher risk of cardiac arrest.

In May 2012 the FDA notified health care providers to consider the presence and quantity of acetate, citrate, and/or acetic acid in dialysate concentrates when determining the patients’ dialysate prescription.

There is a GranuFlo and NaturaLyte Class 1 Recall

Serial numbers for recalled Naturalyte Liquid Acid Concentrate range from:

08-0231-4, 08-1001-0, 08-1201-8, 08-1231-3, 08-1251-1, 08-1301-4, 08-2201-5, 08-2231-2, 08-2251-0, 08-2301-3,08-2351-8, 08-3201-4, 08-3231-1, 08-3251-9, 08-3301-2, 08-4123-1, 08-4223-7, 08-4225-1, 08-4230- 2, 08-4231-0, 08-4323-5, 08-4325-1, 13-1251-1, 13-2201-5, 13-2231-2, 13-2251-0, 13-3231-1, 13-3251-9, 13-4123-1, 13-4220-1, 13-4225-1, 13-4325-

Serial numbers for recalled Naturalyte GranuFlo (powder) Acid Concentrate range from:

OFD1201-3B, OFD1251-3B, OFD2123-3B, OFD2201-38, OFD2220-3B, OFD2223-3B, OFD2225-3B, OFD2231-3 B, OFD2251-3B, OFD2301-3B, OFD2323-3 B, OFD2325-3B, OFD3201-3B, OFD3231-3B, OFD3251-3B, OFD3301-3B

GranuFlo & NaturaLyte is one of the most widely prescribed dry acid products used for dialysis at Fresenius clinics, as well as other hemodialysis centers that purchase their dialysis supplies from Fresenius. It is estimated that 125,000 patients in non-Fresenius clinics are treated with GranuFlo.

Dilaysis Patient Alert

If you, a loved one or someone you care for has been injured by these products contact us for a GranuFlo and NaturaLyte lawsuit.

Bladder Sling Lawyers, Vaginal Mesh Lawsuits

The bladder mesh is a vaginal mesh product primarily used for urinary incontinence. This mesh sling has caused severe complications and bladder mesh lawyers are filing lawsuits. Many women with a bladder mesh do not realize they are eligible to file a vaginal mesh lawsuit.

What is a Bladder Sling?

Urethral sling or bladder sling is used to treat urinary incontinence by placing a sling around the urethra to lift it back into a normal position and to exert pressure on the urethra to aid urine retention. The sling is attached to the abdominal wall. A bladder sling is a mesh device and is part of the vaginal mesh litigation. The complications of a failed bladder sling is increased incontinence or trouble voiding. Many women have needed to self catherize.

Bladder Sling Complications?

According to the July 2011 FDA news release, the most common complications associated with surgical mesh bladder slings is erosion thru the vaginal wall or into the bladder, pain during sexual intercourse, bleeding, infection, perforation of various pelvic organs (bladder, colon, vaginal walls), and urinary incontinence or problems voiding as well as; neuromuscular problems, emotional problems, mesh contraction/shrinkage, and even a reoccurrence of POP and/or SUI.

Bladder sling lawsuits are being filed on a contingency fee basis against the mnaufacturers of the bladder sling:

Bard Avaulta Support System
AMS Elevate Prolapse Repair System
AMS Apogee Vault Suspension System
AMS Perigee System
AMS Monarc Sling System
AMS Sparc Sling System
Ethicon Gynecare Gynemesh
Ethicon Gynecare Prolene Soft Mesh
Ethicon Gynecare Prolift Pelvic Floor Repair System
Ethicon Gynecare TVT Transvaginal Sling
Boston Scientific Pinnacle Pelvic Floor Repair Kit
Boston Scientific Uphold Vaginal Support System
UGYTEX Dual Knit Mesh
Coviden IVS Tunneler Sling

Contact us today.

Stryker Hip Replacement Lawyers, Stryker Hip Replacement Helpline

Adding to the Zimmer and DePuy metal on metal hip replacement Stryker has recalled it s latest metal component hip replacement implant. Stryker has voluntarily recalled the Rejuvenate metal component hip replacement implant and ABG II modular- neck stems
Stryker has voluntarily stopped market distribution of these hip replacements due to increased risk of injury. The hip replacement implants have been shown to fret or corrode, harming body tissue and causing pain and swelling. Other injuries include:

  • Severe inflammatory reactions
  • Pain in the groin
  • metal toxicity ort poisoning
  • high metal levels in the blood
  • need for additional surgery
  • Breakdown of muscles, tendons and other soft tissues in and around the hip joint
  • Loss of surrounding bone
  • Loss of mobility

While other types of hip implants such as those made by Johnson & Johnson and DePuy Orthopaedics Inc. involve a metal ball rubbing against a metal socket, the Stryker Rejuvenate products involve a metal neck inside a metal stem. The Stryker Hip replacement Helpline and hip replacement lawyers are reaching out to all victims of the failed device for a potential multi district litigation.

The products have metal components and although they are not metal on metal run the same risks of chromium and cobalt toxicity poisoning. If you have been injured you are advised to contact your doctor immediately and contact the Stryker Hip Replacement Helpline for a Stryker lawyer

Pradaxa Breaking News, Pradaxa lawyers, Pradaxa Lawsuits, Pradaxa Bleeding

Pradaxa has warnings for excessive bleeding. Pradaxa Helpline is concerned about Pradaxa and the elderly

The Pradaxa Helpline Has Pradaxa Lawyers to Help You

LONDON | Fri May 25, 2012 6:07am EDT

(Reuters) Doctors and patients should be given clearer guidance on how to avoid bleeding risks when using Boehringer Ingelheim s new stroke prevention pill Pradaxa, European regulators said on Friday.

The European Medicines Agency said data continued to confirm the positive benefit-risk balance of the anticoagulant medicine, despite cases of fatal bleeding, but advice on the risks should be strengthened.

Pradaxa is the first in a new class of medicines aimed at replacing the old and problematic drug warfarin. It is designed for use after hip and knee surgery and to prevent strokes in patients with atrial fibrillation, a form of irregular heartbeat common among the elderly.

Rival drugs include Xarelto, from Bayer and Johnson & Johnson, and Eliquis, from Bristol-Myers Squibb and Pfizer.

Pradaxa is an anticoagulant. Anticoagulants effect the clotting time of the blood. Pradaxa is described as a prescription blood-thinning medicine used to reduce the risk of stroke and blood clots in people with atrial fibrillation not caused by a heart valve problem. With atrial fibrillation, part of the heart does not beat the way it should. This can cause blood clots to form, increasing your risk of a stroke. Pradaxa lowers the chance of blood clots forming in your body. There is a chnce of excessive bleeding on Pradaxa that can be fatal.

We can locate a Pradaxa lawyer to help you:

Silicone Breast Implant Claims Lawyers, Silicone Breast Implant Class Action

Breast implant Class Action lawyers Helping women with Dow Corning, Mentor and other Silicone breast implant claims.

Silicone breast implants caused silicone toxicity and Immune deficiency diseases with symptoms of:

  • Muscle Pain -Upper arms, neck, chest, upper back, thighs, buttocks
  • Joint Pain -hands, feet, toes, elbows
  • Pressure headaches
  • Ringing in ears
  • Sun sensitivity & rash; face, neck & upper chest
  • Hives
  • Intermittent tingling in legs, feet, arms, fingers, right upper back, neck and face
  • Many urinary tract and yeast infections
  • Burning lips, mouth, tongue
  • Dry eyes, nose, mouth, and vagina
  • Nausea, heartburn, constipation, diarrhea
  • Insomnia
  • Anxiety

And:

  • Breast Pain
  • Upper and Lower Back Pain
  • dry eyes
  • joint pain and swelling
  • myalgias
  • chronic fatigue
  • Lupus
  • numbness and tingling in extremities
  • photosensitivity
  • Chemical Sensitivities
  • Muscle Pain, Stiffness, Unusual Fatigue
  • Excessive Hair Loss
  • Achy or Swollen Joints
  • Extreme fatigue
  • Skin Rashes
  • Rheumatoid Arthritis
  • Polymyositis-Dermatomyositis
  • Mixed Connective Tissue Disease
  • Scleroderma
  • Sjogren s syndrome
  • Anemia
  • Sensitivity to Sunlight
  • Kidney Problems
  • Fever
  • Difficulty Swallowing or Breathing

Women are still suffering today and settlements are still pending for the Silicone Breast Implant Clas Action. If you currently are registered fo r one of the breast implant settlement manufacturers and need help with your claim call 1 877 522-2123

Texas Lawyers For Victims of Pradaxa, Pradaxa Brain Hemorrhage

Texas pradaxa lawyers filing Pradaxa lawsuits for extensive bleeding and fatalities from pradaxa in Amarillo, Austin, Beaumont , Brownsville, College Station, Corpus Christi, Dallas, Denton, El Paso ,Fort Worth , Galveston, Houston, Huntsville, Killeen, Laredo, Lubbock, Mcallen, Odessa, San Antonio , San Marcos , Texarkana, Texoma, Tyler , Victoria , Waco , Wichita Falls , Logan

The recent death of a man due to a brain hemorrhage caused by a minor trauma has underscored the dangers of the blood thinner drug Pradaxa is very alarming as pradaxa is widely prescibed as a blood thinner for seniors

According to a report at MedPageToday.com on a case study conducted by researchers at University of Utah-Salt Lake City, an 83-year-old man’s condition worsened quickly soon after he was admitted to a hospital after suffering a minor fall. Intracranial Bleeding brain had spread quickly to half his brain, taking just six hours.

According to the Journal of Neurosurgery article, also reported on by Reuters (3/7/12), the subject of the case had been taking Pradaxa for one month when he suffered a seemingly harmless ground-level fall in his home. Upon first being admitted to the hospital, the patient was alert and responsive, showing no signs causing alarm. CT scans showed small, minor hemorrhaging in the man s brain.

Two hours after being admitted to the hospital, however, new CT scans showed that the brain hemorrhaging had progressed. Although doctors made efforts to stop the hemorrhaging, the patient fell into a coma and died.

Researchers concluded, "Imbalance and falls are common in this [elderly] population, and intracranial hemorrhage resulting from even minor trauma may occur with increasing frequency as use of this drug becomes more widespread," (3/6/12). They further noted that there is no way to reverse the effects of Pradaxa in emergency situations, putting patients who suffer relatively minor falls at risk of serious consequences.

Pradaxa has no antidote and can be harmful to a senior population prone to falls. What makes matters worse is that a brain beed has symptoms akin to dementia.

Pradaxa® Internal Bleeding

In November of 2011, a European counterpart to the FDA cited over 250 cases of fatal internal bleeding linked to Pradaxa® (a differently named version of Pradaxa® was on the market in Europe before it was released in the U.S.). The FDA has also received reports of Pradaxa®-associated internal bleeding here in the U.S.

Signs and symptoms of internal bleeding from Pradaxa include:

  • Throwing up blood or vomit that looks like coffee grounds,
  • Unexplained bleeding or bruising,
  • Swelling in the ankles, feet, lower legs, hands and/or arms,
  • Excess fatigue,
  • Nosebleeds, bleeding from the gums,
  • Coughing up blood,
  • Dark colored urine,
  • Gastrointestinal (GI) bleeding,
  • Internal bleeding,
  • Kidney bleeds,
  • Brain hemorrhaging,
  • Cerebral hemorrhage,

Less than a month after European regulators asked doctors to exercise caution about using the Pradaxa bloodthinner, the FDA has decided to investigate post-marketing reports of serious bleeding patients. As of November 6, the European Medicines Agency was aware of 256 cases of serious bleeding that results in patient deaths associated with the Boeheringer Ingelheim bloodthinner.

If you are a caregiver for someone on pradaxa watch them closely and talk to the physician about alternatives. If a loved one has symptoms of internal bleeding and is on pradaxa or you have lost someone due to Pradaxa contact a Pradaxa Lawyer

Whistle blower and Qui Tam Lawyers

Whistleblower and Qui Tam Lawyers,False Claims Act

When an employer is suspected of engaging in illegal actions and benefiting from these actions, an employee may take it upon him or herself to report this to the proper authorities. When this happens, the individual who did the reporting is called a whistleblower. Lawyers of Free Legal Shield have experience helping employees with whistleblower representation for many years. We can protect the rights of employees who are acting as the whistleblower. Qui Tam and whistleblower cases can fall under the category of class action litigation.

Whistleblower

Many whistleblowers find themselves facing problems for the reporting of the suspected activities of their employer. Qui Tam and Whistleblower lawyers assist employees with whistleblower cases and the potential for retaliation or actions taken by the employer.

Qui Tam

Closely related to whistleblower actions, qui tam is a provision of the federal False Claims Act. Under this act, a qui tam action may be filed by a private citizen (usually the whistleblower) charging fraud against a government contractor or a business receiving government funds. The result of this lawsuit is that the citizen may share in the funds that are recovered by the government. Some Qui Tam cses can result in substantial compensation to the whistleblower. Protecting the public against fraud is the purchase of Qui Tam. It is a citizens responsibilty to protect all by reporting illegal theft of Government funds.

Qui Tam in the Health Care Industry

One area in which Qui Tam claims are growing is the health care industry. When an employee has knowledge of fraud involving Medicare, pharmaceutical misconduct or other activity involving government reimbursement or payment for health care, they should speak to a lawyer at our firm for assistance in determining if they may have uncovered a valid claim for wrongdoing and filing a qui tam lawsuit under the False Claims Act. If you report a government fraud or Qui Tam case you may be entitled to substantial compensation.

For more information about whistleblower and qui tam cases contact Free Legal Shield.