Question: A small pharmaceutical firm has just received permission from the
A small pharmaceutical firm has just received permission from the Food and Drug Administration (FDA) to market its new ant cholesterol drug. Although the product has been tested for five years, management believes that serious side effects may still result from its use, and a warning to this effect is being printed on the label. If the company markets this FDA-approved drug, how would you describe its actions from an ethical and legal standpoint?
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