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After reviewing the available scientific evidence, public comments and recommendations from the Tobacco Products Scientific Advisory Committee, the FDA determined that the evidence did not support issuing risk modification orders at this time but that it did support issuing exposure modification orders for these products

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"The currently available treatments have a history of black box warnings and high rates of adverse events that lead to lack of adoption and/or compliance to staying on the treatment," said Bencich

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Bridget McCandless, the foundations president and CEO

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