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These inconsistencies may reflect differences in sample size, exposure assessment approaches, and insufficient adjustment for potential confounders

At one point, Mr

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U of Minnesota Press

131 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." 132 Required reports cannot be overly burdensome and cannot disclose the identity of a patient, except under certain circumstances