FDA Advises Restricted Use of Fluoridated Antibiotics Linked to Serious Nerve Damage

The U.S. Food and Drug Administration (FDA) has issued a drug safety communication in which they advise restricting fluoroquinolone antibiotic use for uncomplicated infections who have other treatment options. An FDA safety review showed that fluoroquinolones are associated with adverse side effects that can be disabling and potentially permanent. These adverse effects involve the tendons,…

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Defective Medical Devices: Stryker Hip Replacements

The Stryker Corp. is based in Michigan, and manufactures around 57,000 products. Their products are all related to the medical and surgical fields, with a focus on reconstructive surgery. In 2009, Stryker recalled three hip replacement products: Rejuvenate Modular-Neck Hip Stems ABG II Modular-Neck Hip Stems Accolade TMZF Plus Hip Stem These three products were…

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Dangerous Drugs: Maryland Risperdal Injury Lawyers

Risperdal is an anti-psychotic used in the treatment of schizophrenia, and is also used in the treatment of bi-polar disorder and certain disorders in patients on the autism spectrum. It is manufactured by Johnson & Johnson, and received FDA approval in 1993. Risperdal – like Invega, another anti-psychotic – are often used in off-label treatments…

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New Study Links Paxil and Prozac to Increased Risk of Birth Defects

A new study published in the British Medical Journal points to a link between pregnant women who take certain anti-depressants and an increased risk of their children developing serious birth defects. As reported by Reuters, researchers surveyed more than 28,000 women to see if they took “Celexa, Lexapro, Prozac, Paxil or Zoloft any time from…

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The Case Against Zofran Manufacturer May Be Worse Than We Thought

Zofran, a popular anti-nausea drug approved for use for cancer patients, has been linked to a number of different birth defects. Around the country families have been bringing lawsuits against GlaxoSmithKline (GSK), the manufacturer of the drug, for marketing Zofran to pregnant women with morning sickness despite the drug never having been tested for its…

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Zimmer Initiates Class 2 Recall of Persona Trabecular Metal Tibial Plate

The Food and Drug Administration issued a press release from Zimmer, Inc., on March 12, 2015 “initiating a voluntary recall of Persona Trabecular Metal Tibial [plate] following an increase in complaints of radiolucent lines and loosening. All sizes and lots of the affected devices are being removed from distribution.” The company asks that any healthcare…

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Medical Devices Contain Antibiotic Resistant “Superbug” CRE

The Centers for Disease Control and Prevention call it the “nightmare bacteria.” It has been implicated in the deaths of hospital patients in both Los Angeles, California and in Seattle, Washington. It is also the basis for new lawsuits against medical device manufacturers. The “superbug” is Carbapenem-Resistant Enterobacteriaceae (CRE), bacteria which “kill up to half…

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