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119 Through such regulations, FDA can also require manufacturers and importers to report if a tobacco product may have caused or contributed to a "serious unexpected adverse experience or any significant increase in the frequency of a serious, expected adverse product experience." 120 Required reports cannot be overly burdensome and cannot disclose the identity of a patient, except under certain circumstances

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"Everyone kind of knows that smoking is bad for you but they don't know how bad, or the extraordinary array of diseases that smoking causes." This report by The Canadian Press was first published April 29, 2024