New Bill Promises To Refine The Lenient 501(k) Medical Device Approval System

Allegedly lenient regulatory practices on behalf of the U.S. Food and Drug Administration (FDA) have allowed several questionable products, most notably transvaginal mesh, to reach interstate commerce. The ambiguity of such regulatory practices has demonstrated a propensity for the release of potentially dangerous devices on the U.S. market. However, a bill recently proposed by…

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Army Continues DMAA Investigation Despite Halt In Public Distribution

Despite a recent moratorium implemented by the federal government on the public distribution of 1,3-dimethylamylamine (DMAA), Army officials are launching their own investigation that will continue to study the effects of the trending bodybuilding supplement. According to a statement made by the Department of Defense last Thursday, the Army plans to gain a deeper…

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New Findings Link Osteoporosis Medications to Unusual Bone Fractures

New research conducted by Per Aspenberg, a professor of orthopaedic surgery at Linkoping University in Sweden, lends weight to the long-suspected link between osteoporosis drugs and unusual bone fractures. He concluded that patients who have been taking osteoporosis medications that contain bisphosphonates for an extended period of time are at a greater risk of…

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Acetaminophen® Lawyer & Lawsuit

Perhaps one of the most prominent pain-relievers on the market today, acetaminophen is used to relieve many forms of mild to moderate pain. Unfortunately, acetaminophen has recently been linked to potentially fatal forms of acute liver damage and/or liver failure. If you or a loved one has been injured by acetaminophen, you should contact…

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Gardasil® Lawyer & Lawsuit

Consumer Alert: To date, there have been over 8,000 adverse effect reports filed regarding Gardasil, as well as 18 deaths allegedly linked to the use of this drug. If you or a loved one has been injured by Gardasil, you should contact our lawyers immediately for a free confidential case evaluation. You may be…

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Reumofan Plus Tablets Recalled Due to the Presence of Undisclosed Ingredients

Regulatory officials at the U.S. Food and Drug Administration (FDA) continue to caution consumers of the transgressions being committed by the dietary supplement industry. Subsequently, several manufactures have attempted to include undisclosed and potentially dangerous pharmaceutical ingredients in their products. Samantha Lynn Inc. has become the latest manufacturer to attempt to taint a dietary…

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Gadolinium Lawyer & Lawsuit

Warning: Gadolinium-based contrast agents may cause a number of severe side effects as well as an extremely serious condition called Nephrogenic Systemic Fibrosis (NSF). If you or a loved one has been injured by gadolinium, you should contact our lawyers immediately for a free confidential case evaluation. You may be entitled to compensation for…

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FDA Encourages Consumers to Report Adverse Reactions Associated with Drugs, Medical Devices and Dietary Supplements

The United States Food & Drug Administration is responsible for the safety and effectiveness of health related products. FDA approves drugs and medical devices based on pre-marketing tests submitted by manufacturers. However, FDA does not do its own testing, and the studies done by companies seeking product approval are often flawed or are too…

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