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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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Population of regions, states, District of Columbia, and Puerto Rico: July 1, 2024 (SCPRC-EST2024-18+POP) [5] Nargis, N., Ghulam Hussain, A

Instead, vape devices heat up the e-liquid, or vape juice, to produce nicotine-containing vapors for people to inhale