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Once a drug has been approved, physicians are free to use it in other populations, for different conditions, and in varying doses from those for which it was approved. Such “off-label” uses are predicated on the assumption that the FDA does not regulate the practice of medicine and that physicians can be relied on to use their own judgment in deciding how to use an approved agent. As long as drugs are safe, well tol- erated, and relatively inexpensive, off-label use generates little concern. But with the ri

Author

William Lopez

Language

EN