Category Archives: Benzocaine

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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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Actos Whistleblower Lawsuit Questions Avandia Researcher's Financial Ties to Takeda

A prominent researcher has been implicated in an alleged cover-up of Actos side effects, according to a report from TheHeart.org. An Actos whistleblower lawsuit unsealed earlier this year has alleged financial connections between the Cleveland Clinic’s Dr Steven Nissen and the maker of Actos “should be considered when analyzing Actos’s ...

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Trial over Ethicon Transvaginal Mesh Begins in California

Pelvic mesh devices have become the subject of safety concerns in recent years amidst reports that they can cause serious, sometimes permanent injuries.

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Dozens Receive Nonsterile Simulated Saline Solution

Dozens-Receive-Nonsterile-Simulated-Saline-Solution

The FDA said last week that more than 40 patients had received intravenous simulated saline that was not sterile and was not intended for human use.

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Johnson & Johnson Facing More Metal-on-Metal Hip Implant Woes, as DePuy Pinnacle Complaints Rise

Having already spent around $3 billion on its DePuy Orthopaedics ASR hip implant recall, Johnson & Johnson is facing another potential debacle involving a metal-on-metal version of its Pinnacle Hip Replacement System. According to a report from Reuters, Johnson & Johnson and its DePuy unit already face some 1,600 metal-on-metal ...
Conspiracy Claims in Talcum Powder Case Survive Motion to Dismiss

Conspiracy Claims in Talcum Powder Case Survive Motion to Dismiss

E. District of Missouri denied motion to dismiss conspiracy claims. Lawsuit alleges the defendants conspired to misrepresent true dangers with use of talcum powder.

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1,000+ Australians Join DePuy ASR Hip Implant Class Action Lawsuit

A class action lawsuit filed in Australia over DePuy Orthopaedics’ recalled metal-on-metal ASR Hip Implants has signed up more than 1,000 plaintiffs. The attorneys representing the Australian ASR Hip Implant lawsuit plaintiffs recently told The Courier-Mail that damages in the lawsuit are expected to be worth more than $200 million. One ...

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Actos Bladder Cancer Lawsuit Filed by West Virginia Resident

Actos (pioglitazone) continues to be named in lawsuits alleging long-term use of the type 2 diabetes drug caused patients to develop bladder cancer. Just last week, the national law firm of Parker Waichman LLP filed suit against Takeda Pharmaceuticals on behalf of a West Virginia man who developed bladder cancer ...

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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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Canadian Study Confirms Actos Bladder Cancer Risk

A new study conducted by Canadian researchers has found that users of the type 2 diabetes drug, Actos (pioglitazone), may face a higher risk of developing bladder cancer than first thought. The study, published in the British Medical Journal, found that taking Actos for two years doubles the likelihood ...

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FDA Takes Action Against Eardrops with Unapproved Ingredients

FDA Takes Action Against Unapproved Eardrops

The Food and Drug Administration (FDA) has issued a warning to parents about prescription eardrops that contain unapproved ingredients that can lead to dangerous side effects. The unapproved prescription eardrops contain active ingredients such as benzocaine and hydrocortisone, and have … Continue reading

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FDA Advises Against Topical Medications for Babies’ Teething Pain

The Food and Drug Administration (FDA) has issued a warning to parents about the dangers of using topical pain medication for babies’ teething pain, citing concerns about serious side effects, even death. The FDA issued a safety warning in June … Continue reading

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FDA Says Benzocaine Products Unsafe for Teething Babies

U.S. health regulators have again warned that benzocaine is not a safe remedy for teething babies.  According to a report from Health Day News, the U.S. Food & Drug Administration (FDA) has warned that benzocaine gels and liquids can lead … Continue reading

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FDA Issues Warning for Benzocaine Teething Remedies

The U.S. Food & Drug Administration (FDA) just issued a warning on some teething remedies such as Anbesol and Oragel. These topical pain relievers are typically rubbed on the gums of teething babies and can lead to a serious condition … Continue reading

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Benzocaine Blood Disorder Prompts Warnings in U.S., Canada

< "http://www.yourlawyer.com/topics/overview/Benzocaine-Spray-Gel-Liquid-Methemoglobinemia-Injury-Lawsuit">Benzocaine, the active ingredient in popular teething medications like Anbesol, Hurricaine, Orajel, Baby Orajel, and Orabase, has been the subject of safety warnings in the U.S. and Canada because of its association with a rare blood disorder called methemoglobinemia. … Continue reading

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Anbesol, Orajel, Orabase Other Benzocaine Products Linked to Rare Blood Disorder, FDA Warns

U.S. health regulators warned today that < "http://www.yourlawyer.com/topics/overview/Benzocaine-Spray-Gel-Liquid-Methemoglobinemia-Injury-Lawsuit">benzocaine liquids and gels used to treat mouth and gum pain, including Anbesol, Hurricaine, Orajel, Baby Orajel, Orabase and store brands, have been associated with a potentially deadly complication called methemoglobinemia. The warning … Continue reading

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