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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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Tentative Ohio Fracking Regulations Criticized as too Lax

Lawmakers in Ohio have tentatively passed new regulations governing hydraulic fracturing (fracking) drilling but they’ve immediately been criticized for being too favorable to the natural gas and oil industries.

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Former Executives Accuse Health Technology Firm of Fraud

Former Executives Accuse Health Technology Firm of Fraud

Former NantHealth executives claim that the company made fraudulent claims about the reliability of its system, which links patient information gathered by the devices.

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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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Bronx Teenager Killed in Hit-and-Run, Second Teen Injured

A Port Jefferson Station man was killed on Wednesday in a single-vehicle crash on the Northern State Pkwy in Dix Hills west of Exit 42. He was driving a Nissan Altima.

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Retailers Accused of Selling Fraudulent Herbal Supplements

Major Retailers Accused of Selling Fraudulent Herbal Supplements

The NYS attorney general’s office has accused four national retailers of selling fraudulent dietary supplements.

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Majority of Metal-on-Metal Hip Implant Failures Occur within Two Years, Study Finds

A newly published metal-on-metal hip replacement study is reporting that the majority of failures occur early, within two years of surgery. The study, published in the journal Orthopedics, is just the latest to indicate that close follow-up of metal-on-metal hip implant patients is warranted.

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Medtronic Plans Layoffs, as Infuse Bone Graft Controversy Continues to Weigh on Spinal Business

Medtronic’s spinal division continues to take a huge hit thanks to the controversy surrounding its Infuse Bone Graft product. According to a report from MassDevice.com, the company’s latest earnings report stated that the division saw Infuse sales decline 26% in the first quarter of 2012, and now Medtronic is talking ...

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DeflateGate’s Effects Impact Legal Gambling and 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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Geodon the antipsychotic drug can Cause Deadly Skin Reaction

Geodon can Cause Deadly Skin Reaction, FDA Warns

The FDA has required a new warning label for the antipsychotic drug Geodon (ziprasidone) to include the risk of a potentially fatal skin reaction.

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Darvon, Darvocet Pulled From Market Due to Heart Risks

The propoxyphene-based painkillers are being pulled from the market today because of their association with serious or even fatal Darvocet and < "http://www.yourlawyer.com/topics/overview/darvon">Darvon side effects (namely heart rhythm abnormalities). The US Food & Drug Administration (FDA) is also asking the manufacturers … Continue reading

Posted in Pharmaceuticals |

Darvon-N Recalled In Canada

Collaborating with Health Canada (HC), Paladin Labs Inc., maker of Darvon-N (dextropropoxyphene, also known as propoxyphene), decided to voluntarily recall and withdraw all lots of the medication from the Canadian market and discontinue sales. Last month, the US Food & … Continue reading

Posted in Pharmaceuticals, Product Recalls, Recalled Drugs |

Darvon, Similar Painkillers to Have Stronger Overdose Warnings

The makers of Darvon, Darvocet and other painkillers that contain propoxyphene are being required to strengthen the drugs’ labels, including their boxed warning, to emphasize the potential for overdose. However, the Food & Drug Administration (FDA) has rejected a petition … Continue reading

Posted in Pharmaceuticals |

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 |

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 |

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 |

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