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Study Linking Z-Pak to Increased Death Risk Being Reviewed by FDA

The U.S. Food & Drug Administration (FDA) is reviewing a new study that reported an increased risk of sudden, heart-related deaths among people using the antibiotic Zithromax (azithromycin), known popularly as Z-Pak. In a statement issued late yesterday, the FDA said patients being treated with Zithromax should not stop taking ...

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Do Vitamin Drinks Pose Health Risks?Do Vitamin Drinks Pose Health Risks?

Do Vitamin Drinks Pose Health Risks?

Scientists are concerned vitamin drinks are contributing to levels of vitamins and other nutrients that are not only unnecessary, but potentially harmful.

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Bisphosphonate Study Confirms Atypical Thigh Fracture Risk

New research has confirmed the link between bisphoshonates, such as Fosamax, and atypical femur fractures, a type of thigh fracture that occurs spontaneously, without any major leg injury. The study, published in the Archives of Internal Medicine, also found that the risk of atypical thigh fractures increases the longer a ...

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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. According to press release issued Jan. 7, a resolution was introduced by Council Member Margaret Chin, Council Speaker Melissa Mark-Viverito and Council Members Paul Vallone and I. ...

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Soda Consumption Causes Early Puberty & Girls’ Cancer Risk

Soda Consumption Causes Early Puberty and Increases Girls’ Cancer Risk

Drinking just one-and-a-half cans of sugar-sweetened soda a day can bring on early puberty in girls and increase their breast cancer risk.

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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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Metal-on-Metal Hip Replacement Device

Smith & Nephew’s Birmingham Metal-on-Metal Hip Replacement Device

Wright Medical Inc. took steps in to 2006 to convince the U.S. Food & Drug Administration (FDA) to reject pre-market approval of rival Smith & Nephew’s Birmingham metal-on-metal hip implant. Wright Medical, which makes two metal-on-metal hip replacement devices, the Conserve and the Lieneage device, filed a citizen petition ...

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DeflateGate’s Effects Impact Legal Gambling & the Economy

DeflateGate’s-Effects-Impact-Legal-Gambling-and-the-Economy

The NFL has initiated a probe into the New England Patriots following allegations that the team intentionally used overly deflated footballs.

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FDA Advisors Set to Examine Metal-on-Metal Hip Implant Safety Concerns

Thousands of people with metal-on-metal hip implant devices could soon get some answers from the U.S. Food & Drug Administration (FDA) about the dangers they face. Tomorrow, the agency will convene a panel of outside medical experts to examine the safety record of metal-on-metal hip replacements, and recommend the ...

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Federal Judge Certifies Medtronic Infuse Shareholder Class Action Lawsuit

A shareholder lawsuit alleging Medtronic Inc. illegally promoted the off-label use of its Infuse bone growth product has been granted class action status by U.S. District Judge Paul Magnuson of Minnesota. According to a report from Law360.com, the Medtronic Infuse off-label promotion lawsuit was filed by several institutional investors on ...

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FDA Panel Urges Darvon Ban

The Darvon debate continues, but  U.S. Food and Drug Administration (FDA) advisors are recommending the painkiller be pulled from the market.  USA Today reported that following a hearing about the popular pain drug, a FDA panel voted for Darvon recall … Continue reading

Posted in Legal News, Pharmaceuticals |

Consumer Watchdog Group, Public Citizen, Petitions FDA to Ban All Darvon Products

Public Citizen “a national, nonprofit consumer advocacy organization founded in 1971 to represent consumer interests in Congress, the executive branch and the courts” has filed a lengthy formal petition (http://www.citizen.org/publications/release.cfm?ID=7420) with the Food and Drug Administration “pursuant to the Federal … Continue reading

Posted in Health Concerns, Legal News |

Darvocet Wrongful Death Lawsuit Filed by Estate of Louisiana Woman

The family of a Louisiana woman who suffered a fatal heart attack has filed a wrongful death lawsuit against the makers of < "http://www.yourlawyer.com/topics/overview/darvocet">Darvocet. This latest Darvocet lawsuit names Eli Lilly and Co., Xanodyne Pharmaceuticals Inc., Vintage Pharmaceuticals Inc., Qualitest … Continue reading

Posted in Darvon / Darvocet, Pharmaceuticals |

New Darvocet Class Action Lawsuit Filed in Louisiana

The maker of < "http://www.yourlawyer.com/topics/overview/darvocet">Darvocet is facing a class action lawsuit that alleges the manufacturer’s neglect to warn patients of the drug’s—and its generic equivalent’s—risks and side effects. Propoxyphene is an opioid painkiller that was first sold as Darvon in … Continue reading

Posted in Darvon / Darvocet, Pharmaceuticals |

Darvocet Lawsuit Filed on Behalf of New York Woman

A < "http://www.yourlawyer.com/topics/overview/darvocet">Darvocet lawsuit has been filed on behalf a 31-year-old New York woman who says the recalled painkiller caused her to suffer a near-fatal cardiac arrhythmia. The plaintiff is being represented by the national < "http://www.yourlawyer.com/">personal injury law firm … Continue reading

Posted in Legal News, Pharmaceuticals |

Darvocet Class Action Lawsuit Says Painkiller Caused Heart Attack

A propoxyphene-containing painkiller has been named in a Darvocet class action lawsuit filed by a woman who claims it caused her to suffer a heart attack. Darvocet, as well as Darvon, were pulled from the market by Xanodyne Pharmaceuticals Inc. … Continue reading

Posted in Pharmaceuticals |

Group Wants FDA to Ban Painkiller

Propoxyphene, the addictive prescription painkiller sold under names that include Darvon and Darvocet is too risky to stay on the market, says Public Citizen, a consumer advocacy group suing the US Food and Drug Administration (FDA). Public Citizen petitioned the … Continue reading

Posted in Legal News, Pharmaceuticals |

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