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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

Theres been a number of cases throughout the country under that very scenario

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Truth Initiative launched a public education truth education and prevention campaign, The Truth About Opioids , in partnership with the Office of National Drug Control Policy and the Ad Council, designed to help young people understand the dangers of opioid misuse