I disagree, I feel the bolded statement is the most powerful in the entire summation. The
FDA labeling, adverstising and package insert requirement is different for direct to consumer ads as opposed to medical professional literature. For direct to consumer ads, literature there only has to be "fair and balanced" disclosure between good and bad(which is why at the end of every Rx commercial they quickly mention a list of the 5 or 10 most reported side effects). For the medical professional ads, literature, labeling and package insert info, a much higher standard of "FULL DISCLOSURE" is REQUIRED by law. Therefore, in medical literature, EVERY pertinent fact, good or bad, ever found, must be included by the manufacturer. . So the Fact that the manufacturers of
NRT's did NOT include ANY info about TSNA's in their medical literature(doctor ad's, professional package inserts, labeling etc..) shows, without a shadow of a doubt, that
FDA did not consider this fact to have any clinical significance AT ALL in the past. Therefore, they did not require the manufacturers of
NRT's to have to even mention it in their professional literature. If the
FDA truly thought TSNA's were any type of short or long term threat, they would have required every
NRT manufacturer to specifically reference the TSNA content and warning in their professional literature. So basically the bolded statement you referenced in the summation proves the
FDA is just making this TSNA hysteria up after the fact.
Bookmarks