Monthly Archives: November 2006

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FDA Gives 7 Companies Go Ahead To Market Generic Plavix

The U.S. Food & Drug Administration (FDA) just gave seven companies the go-ahead to market generic Plavix. Plavix is a blood thinner prescribed for the prevention of blood clots, heart attacks, and which has been linked to serious side effects such as the heart attacks and strokes it is supposed to ...

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Transvaginal Mesh a Nightmare for Thousands of Women

Thousands of women who have received transvaginal mesh surgical implants to treat stress urinary incontinence (SUI) and pelvic organ prolapse (POP) are now living a nightmare, thanks to debilitating pain, bleeding, infection and other serious complications. According to the Sun-Sentinel, many of the women injured by transvaginal mesh claim ...

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Whistleblower Wins Retaliation - Canaveral National Seashore

Whistleblower Wins Retaliation Lawsuit

A whistleblower who reported misconduct at Canaveral National Seashore has won a retaliation ruling against the U.S. Department of Interior, Florida Today reports.

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Pradaxa Named in Most FDA Adverse Event Reports for Deaths, Hemorrhage, Kidney Failure and Stroke

The controversial blood thinner, Pradaxa, surpassed all other drugs monitored by the U.S. Food & Drug Administration (FDA) in adverse event reports made to the agency last year. According to the Institute for Safe Medicine Practices’ (ISMP) latest QuarterWatch report, Pradaxa also topped the list for reports of deaths, ...

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Indiana Woman Alleges Serious Injuries From Transvaginal Mesh Products

Parker Waichman LLP, a national law firm, just filed a lawsuit on behalf of a woman who suffered injuries after receiving transvaginal mesh implants. The lawsuit suit alleges that the transvaginal mesh created an unreasonable risk and directly caused her injuries.

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Actos, Avandia May Up Risk for Diabetic Macular Edema

A West Virginia man fitted with a metal-on-metal version of DePuy Orthopaedics’ Pinnacle Hip Implant System has filed suit against the company and its parent, Johnson & Johnson, alleging the device caused him to suffer pain and elevated cobalt levels. The Plaintiff is being represented by the national law ...

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FDA Panel Takes up Metal-on-Metal Hip Implant Safety Today

The Food and Drug Administration (FDA) is convening a meeting starting today to help decide the future of metal-on-metal hip implants following high-profile recalls and mounting questions about their overall safety.

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Actos Bladder Cancer Lawsuits Continue, New Complaint Filed by Tennessee Resident

Actos bladder cancer lawsuits continue, with a new complaint filed by a resident of Tennessee. The national law firm, Parker Waichman LLP, represents the Tennessee man who alleges that Actos caused his bladder cancer.

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Cancer Groups Call for E-cigarettes Regulation/Research

Two Leading Cancer Groups Issue Call for Regulation of E-cigarettes and Research on Health Risks

In a joint statement, the American Society of Clinical Oncology and the American Association for Cancer Research have called on the federal government to move quickly to regulate e-cigarettes and increase research on their health effects. These leading research and treatment organizations asked the Food and Drug Administration (FDA) to make ...

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Parker Waichman Representing Another Louisiana Plaintiff in Actos Bladder Cancer Lawsuit

A Louisiana man has become the latest to claim that his taking the type 2 diabetes drug Actos resulted in developing bladder cancer. He has filed a lawsuit against the Japanese manufacturer of the drug and the marketer of it in the U.S., claiming they failed to warn about this ...

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Katrina Victims Win Latest Court Battles

Thousands of victims of Hurricane Katrina finally have some good news to celebrate: A U.S. District Court judge ruled yesterday that the Federal Emergency Management Agency (FEMA) must resume making housing-relief payments to those displaced by the disaster. In handing … Continue reading

Posted in Consumer Fraud, Legal News |

Medtronic’s Bid to Dismiss Lawsuits Denied

Minneapolis-based Medtronic, manufacturers of a controversial implantable cardioverter defibrillator (ICD), had their motion for summary judgment denied in U.S. District Court, meaning that the company may still have to face personal-injury lawsuits regarding their allegedly faulty product. The company announced … Continue reading

Posted in Health Concerns, Legal News |

Health Canada Issues New Warning Regarding Tamiflu

The popular antiviral drug Tamiflu is under fire again, this time from Health Canada. The Canadian government issued a new safety advisory today, warning consumers that < "http://www.yourlawyer.com/topics/overview/tamiflu">Tamiflu may be linked to hallucinations and abnormal behavior, including self harm. In … Continue reading

Posted in Health Concerns, Legal News |

Health Canada Issues Health Advisory for Rituxan

In conjunction with drug maker Hoffmann-LaRoche, Health Canada has issued new safety information regarding < "http://www.yourlawyer.com/topics/overview/rituxan">Rituxan, which is used in the treatment of non-Hodgkin’s lymphoma (NHL) and rheumatoid arthritis. According to the company, post-market and clinical studies have revealed reports … Continue reading

Posted in Health Concerns, Legal News |

FDA Announces New Warning for Methadone Patients

According to the U.S. Food and Drug Administration, patients treated with methadone are susceptible to life-threatening alterations in their breathing and heartbeat–and, in some cases, even death. The FDA issued its latest health advisory yesterday, warning patients of potential problems … Continue reading

Posted in Health Concerns, Legal News |

AstraZeneca Warned by FDA About Misleading Seroquel Marketing Material

The U.S. Food and Drug Administration has sent a warning letter to drug maker AstraZeneca, claiming that some of the company’s promotional material for Seroquel contains “false or misleading” information. According to the FDA, AstraZeneca failed to adequately detail the … Continue reading

Posted in Health Concerns, Legal News |

Volvo Recalls 360,000 Autos

The National Highway Traffic Safety Administration (NHTSA) has ordered a recall of approximately 360,000 Volvo automobiles due to faulty software in the cars’ electronic throttle-control units. The software flaw affects the vehicle speed control and may cause the car to … Continue reading

Posted in Product Recalls, Recalled Vehicles |

Another Contact-Lens Solution Recalled

On Tuesday, the U.S Food and Drug Administration announced a voluntary recall by Advanced Medical Optics Inc. (AMO) of nearly 3 million units of its 12-ounce < "http://www.yourlawyer.com/topics/overview/complete_moistureplus_lens_solution">Complete MoisturePLUS contact-lens solution and Complete MoisturePLUS Active Packs because of bacterial-contamination fears. … Continue reading

Posted in Health Concerns, Legal News |

Drug-Research Firm SFBC International Faces Class-Action Suit

SFBC International, now known as PharmaNet Development Group, has been named as a defendant in a securities class-action suit filed yesterday in the United States District Court of New Jersey. Plaintiffs are accusing SFBC and its senior officers of multiple … Continue reading

Posted in Legal News |

Mattel Recalls Polly Pocket Dolls

The U.S. Consumer Product Safety Commission (CPSC) today announced that California-based Mattel Inc. is voluntary recalling 2.4 million units of its Polly Pocket magnetic play sets. The CPSC has received approximately 170 reports of small magnets coming loose from these … Continue reading

Posted in Health Concerns, Legal News, Product Recalls |

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