Contributor (866) 529-2400 The U.S. pharmaceutical industry and its federal regulator, the U.S. Food and Drug Administration, have a lot on their plates. Brand-drug makers must pump out new medications, to stay fiscally afloat, as their drug patents fall like dominoes, which the generic competitors pick up and run for their lives with. At the same time, there is a craft in the drug makers repertoire of survival skills that is no less important than managing the books, developing the product per FDA rules, and defending themselves from pharmaceutical injury lawsuits. This craft is the Side Effects Shuffle, the art of applied science that often does not fully vet a drug before it is marketed. The dance is about mitigating health risks in medications. The shuffle, for the most part, takes place after the damage is done and after the patients hire a personal injury attorney, at Reich and Binstock or elsewhere, to help them to recover their damages. It takes an interrelationship of pharmaceutical corporate interests to address some of these serious risks. Here is one archetypal Skip to My Lou, which follows a summary of a particular drugs recent regulatory history. Bayer makes the combination oral contraceptive, or … Continue reading
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