dunbarton tobacco & trust David Lafferty Joins Dunbarton Tobacco & Trust "Deep

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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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Even so, addiction experts unaffiliated with the study have described the findings as exciting and potentially paradigmshifting

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