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"While a new tobacco product can be legally sold if FDA authorizes it through the premarket tobacco product application (PMTA) pathway, seeking FDA authorization of the product through the optional MRTP pathway presents a meaningful harm reduction opportunity for manufacturers to communicate that certain products present a lower risk of tobacco-related disease, providing adults who smoke with the ability to make more informed decisions," the agency wrote in a Tuesday news release

Adults with mental illnesses manifesting within the past month were the most likely to smoke and the least likely to quit

Treatment and outcomes PCR, polymerase chain reaction.

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