Clark County residents, as well as every other American consumer of prescription drug products, should consider whether the FDA is too cozy with the industry it regulates particularly in light of...
Diana Levine's arm was amputated after she developed gangrene from an injection of Wyeth's anti-nausea drug Phenergan. This week a brief was filed on Ms. Levine's behalf with the United States...
In this blog, I continue our series on Tardive Dyskinsia, Tardive Dystonia and Akathasia, Physicians are familiar with Tardive Dyskinesia through their experiences with drugs such as Thorazine and...
In the last blog, I briefly discussed Digitek. The active ingredient in Digitek is Digoxin. Digoxin overdose and digitalis toxicity can cause serious and life-threatening personal injury and...
Our last blog entry discussed a severe neurological condition a person can get when ingesting Reglan (or its generic metoclopramide). If you read our other blog entries, you know this condition is...
Recently, our firm achieved the largest personal injury verdict in the history of the state ($134M) against drug-maker Wyeth for three women who proved to a jury that their breast cancer was caused...
FDA adds black box warning to conventional antipsychotics under new found power of Food and Drug Amendments Act.
Who is monitoring drug and medical device safety? If the FDA is understaffed and underfunded will the Sentinel Initiative work?
After a few years in this business of representing patients/clients who have been injured by defective drugs, it appears that:1. The FDA doesn't protect consumers, though it might try2. All should know that the FDA doesn't test drugs3. The drug companies are in it for profit first, helping people second (no surprise)4. You shouldn't take any new drug until it has been out on the market...
Yesterday, I commented on the FDA's difficulties in meeting its mandate as described in the FDA Report on Science and Technology published on December 3, 2007, by the FDA Science Board Advisory Committee. Despite the severe limitations on the FDA's abilities set forth in that report, the FDA is forging ahead with proposed "Guidance for Industry" which would allow drug companies to distribute...
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