Monthly Archives: November 2013

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64 More Plavix Patients File Suit Over Bleeding Side Effects

Another Plavix lawsuit has been filed on behalf of 64 Plavix patients who allege bleeding side effects. Plavix (clopidogrel) is a blood thinner prescribed for the prevention of blood clots and heart attacks, and has been linked to serious side effects, such as the heart attacks and strokes it is ...

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Sleep Aids Can Increase Alzheimer’s Risk

A new study has found that over-the-counter sleeping aids and anti-allergy medicines can increase the risk of Alzheimer’s disease.

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First DePuy ASR Hip Implant Lawsuits Head to Trial in December, January

The first trials involving lawsuits filed against DePuy Orthopaedics by recipients of its recalled ASR Hip Implants will begin later this year, and early next year. The first is slated to start on December 3, 2012 in state court in Las Vegas, Nevada. A second DePuy ASR hip implant lawsuit ...

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National Law Firms Calls for More FDA Action on Actos Bladder Cancer Threat

A national law firm is not satisfied with the way the U.S. Food & Drug Administration (FDA) has handled warnings regarding Actos (pioglitazone) bladder cancer risks. In a statement published today, Parker Waichman LLP called on the FDA to compel Takeda Pharmaceuticals, the maker of the type 2 diabetes drug, ...

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Medtronic Infuse Lawsuit Alleges Off-Label Use Cause Painful Complications

A man in Louisiana has filed suit against Medtronic Inc. over injuries allegedly cause by off-label use of its Infuse Bone Graft product. The plaintiff, who received Infuse during transforaminal spinal lumbar fusion surgery, claims that the bone growth protein caused unwanted bone growth along his spine, worsening the back ...

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Research Suggest Fracking Chemicals Can Pollute Aquifers

A new study suggests fluids used during the hydraulic fracturing (fracking) process could migrate through underground fractures and contaminate water aquifers.

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Lawsuit Alleges Bi-Lateral DePuy ASR Hip Implant Resulted in Elevated Chromium and Cobalt Levels, Need for Revision Surgery

DePuy Orthopaedics and its parent, Johnson & Johnson, continue to be named in lawsuits by metal-on-metal hip replacement recipients who suffered severe injuries, including elevated chromium and cobalt levels, allegedly due to recalled ASR hip implant devices. Most recently, the national law firm of Parker Waichman LLP filed suit on ...

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Study Finds SSRI Antidepressant Side Effects Outweigh Their Benefits

A new study is raising more concerns about the safety of commonly used antidepressants, including selective serotonin reuptake (SSRI) inhibitor antidepressants. Investigators who conducted the study, which is published in the journal Frontiers in Psychology, posit that increased knowledge of the negative effects of SSRIs and other antidepressants could reduce ...

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Metal-on-Metal Hip Implant Lawyer Takes Issue with Statements Made by DePuy Orthpaedics Official During FDA Meeting

An attorney with a national law firm that represents victims of alleged metal-on-metal hip implant injuries has expressed dismay at some statements made last week regarding the regulation of all-metal hip replacement devices by an official with DePuy Orthopaedics. According to Daniel Burke, Senior Litigation Counsel at Parker ...

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New York City Council Calls for Zadroga Act to be Renewed

New York City Council Calls for Zadroga Act to be Renewed

New York City Council members are calling for the Zadroga Act, which provides compensation and medical treatment to 9/11 victims, to be renewed.

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Be Careful When Shopping for Toys This Holiday Season

beware-of-dangerous-toys-holiday-shoppers

Consumer experts warn shoppers to be aware this holiday season of dangerous toys that are still on store shelves and which are putting children at risk of injury. The U.S. Public Interest Research Group (PIRG) found that hazardous toys are … Continue reading

Posted in Children's Toys, Consumer Fraud, Defective Products, Health Concerns |

FDA Deems Hospira Recall of its GemStar Infusion System a Class I

hospira-recall-class-one-infushion-pumps

The U.S. Food and Drug Administration (FDA) just announced a Class I recall of Hospira Inc.’s GemStar Infusion System, over a pressure sensor calibration drift. The FDA’s Class I recall designation means that the situation is one in which there … Continue reading

Posted in Defective Medical Devices, Defective Products |

FDA Reviewing Efficacy of “Morning After Pill” in Women Weighing Over 165 Pounds

morning-after-pill-effectiveness

United States health regulators just announced that they are reviewing the efficacy of Plan B emergency contraceptive pills as they may not offer the same benefits in women who weigh more than 165 pounds. In the U.S., the Plan B … Continue reading

Posted in Health Concerns, Pharmaceuticals |

LG TVs Spying on Consumers

lg-smart-tv-spying-on-customers

Recently, the maker of LG Electronics’ Smart TV admitted to collecting information on consumers’ viewing habits, apparently without consumer knowledge. LG’s new line of Smart TVs collect viewer data to customize the advertising seen on their screens, according to Law … Continue reading

Posted in Consumer Fraud |

Mental Health Risks Tied to Steroid Injections Meant to Stop Premature Birth

steroid-injections-before-birth-mental-health-problems

A new study reveals that steroid injections used to prevent premature birth might increase future risks of behavioral and emotional problems in the developing children. Expectant mothers who might give birth prematurely are often treated with an infusion of glucocorticoids. … Continue reading

Posted in Health Concerns, Pharmaceuticals |

FDA Orders Genetic Testing Firm to Cease DNA Analysis Service Sales

dna-testing-halted-by-fda

The U.S. Food and Drug Administration (FDA) has demanded 23andMe, a DNA testing service, to immediately stop selling and marketing its services until the agency gives the firm clearance to do so. The FDA is seeking to stop the sales … Continue reading

Posted in Defective Medical Devices, Defective Products, Health Concerns, Pharmaceuticals |

FDA Issues Drug Safety Statement Over Meridian Medical Technologies Auto-Injectors

meridian-duo-dote-injector-extended-expire-date

The U.S. Food and Drug Administration (FDA) just announced that it has been made aware of a supply disruption of auto injectors for Atropen (atropine),
DuoDote (atropine/pralidoxime chloride),
morphine sulfate,
pralidoxime chloride, and 
diazepam. The auto injectors involved are manufactured by Meridian Medical … Continue reading

Posted in Pharmaceuticals |

Diabetes Drug-Pancreatitis Link Supported in Another Study

mimetic-diabtes-linked-to-pancreatitis

Another study has made a connection between Type 2 diabetes drugs known as incretin mimetics and increased rates of developing pancreatitis, a known precursor to pancreatic cancer. Incretin mimetics, are GLP-1-based diabetes therapies and include Byetta and Bydureon (exenatide); Victoza … Continue reading

Posted in Byetta Cancer, Pharmaceuticals |

Amgen’s Aranesp Claims Get FDA Attention for Overstating Benefits, Minimizing Risks

aranesp-anemia-drug-misleading-claims

The U.S. Food and Drug Administration (FDA) just wrote to drug maker, Amgen Inc., about misleading marketing claims concerning its anemia drug, Aranesp (darbepoetin alfa). The letter, not quite as serious as an agency warning letter, scolded the drug maker … Continue reading

Posted in Pharmaceuticals |

Cameras Catching Nursing Home Abuse Lead to Controversy

cameras-monitor-nursing-home-abuse

Nursing home abuse is among the most devastating of horrors targeting our older, vulnerable loved ones. Recently, a case in which a small camera—meant to catch a petty thief—caught a loved one being abused and taunted, increasing awareness of both … Continue reading

Posted in Legal News, Nursing Home Abuse |

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