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Articles Posted in Product Liability

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Arkansas Fines Johnson & Johnson $1.1 Billion in Risperdal Case

An Arkansas judge fined Johnson & Johnson and a subsidiary more than $1.1 billion for downplaying and concealing risks associated with the antipsychotic drug Risperdal. Judge Tim Fox ruled that Janssen Pharmaceuticals Inc. and its parent company must pay $5,000 for each of 240,000 Risperdal prescriptions the state Medicaid program…

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Acetaminophen Tylenol Linked to Severe Liver Damage.

Tylenol is the most popular pain killer in America, with billions of the tablets and capsules sold each year. Acetaminophen is the generic name for Tylenol, and is found in well over 200 commonly available over the counter medications, including DayQuil® and Tylenol®. Acetaminophen-related liver injuries (Acetaminophen Injury) result in…

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Bayer’s Natazia Contraceptive Associated with Deadly Side Effects

Natazia (estradiol valerate and estradiol valerate/dienogest), a fourth generation oral contraceptive made by pharmaceutical giant Bayer HealthCare Pharmaceuticals, Inc, was FDA-approved on March 15, 2012, for the treatment of heavy menstrual bleeding. In February 2012, the FDA gave Natazia a Black Box Warning regarding “Thromboembolic Disorders and Other Vascular Problems.”…

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No Cancer Risk Seen in Metal-on-Metal Hips

According to a medical study, patients who received metal-on-metal hip replacements are at no greater risk of developing cancer after a seven-year period than the general population. The research is published in the British Medical Journal, and recommends that longer-term review is needed of the effect of metal particles released…

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DePuy MITCH, Stryker Accolade Hip Replacement Combo Warning

There is a new warning from the U.K. health officials, that states patients who received combination DePuy MITCH and Stryker Accolade metal-on-metal hip replacement components are experiencing a high failure rate. The U.K. Medicines and Healthcare products Regulatory Agency (MHRA) issued a medical device alert (pdf) on April 2, stating…

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The Problem with Pradaxa

In December of 2011, The U.S. Food and Drug Administration (FDA) issued a safety announcement, that it was “evaluating post-marketing reports of serious bleeding events in patients taking Pradaxa (dabigatran etexilate mesylate). Pradaxa is a blood thinning (anticoagulant) medication used to reduce the risk of stroke in patients with non-valvular…

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