Guest guest Posted March 26, 2004 Report Share Posted March 26, 2004 FDA-sanctioned manslaughter? Sure Again, you've heard me talk at great length about the antidepressant/suicide link (Daily Dose, 12/26 and 12/30/2003) in the past, but there's a more ominous component to this correlation that I've never mentioned before - and it relates directly to the " selective reporting " topic I discussed above... According to a recent Washington Post online article, makers of several of the most popular " happy pills " have refused to divulge any details about the bulk of the antidepressant trials they've conducted on children. As I've already explained, hiding negative study results is par for the course in the drug biz. But in this case, such conduct clearly denies doctors and parents the facts they need to make informed decisions about children's mental health. Why is this so important all of a sudden? Because of the abundance of evidence suggesting that taking antidepressant drugs might cause kids to KILL THEMSELVES. Not break out in a rash, gain a few pounds or develop sleeping problems - but take their own lives. This tragic correlation has been speculated about before, as several instances of seemingly antidepressant-related suicide have occurred in recent years. In one 2004 trial for the antidepressant duloxetine, a 19- year-old female test subject hanged herself in the drug company's research lab at Indiana University. And here's the kicker: She WASN'T EVEN DEPRESSED; she was just a perfectly healthy, random participant in the trial. Not surprisingly, the incident prompted 19 participants and study volunteers to quit the test in fear for their own lives. The bottom line is this: As long as drug companies are free to submit for review and publication only that research which is flattering to their patented medications, we'll never really know the truth about what these chemicals are doing to us - or NOT doing to us (like healing us). By looking the other way and allowing pharmaceuticals makers to keep negative findings about drugs under wraps, the FDA becomes complicit in every adverse occurrence that happens because of these drugs - including deaths. This is manslaughter, in my eyes. I say it's high time the FDA changed its rules to require drug companies to submit ALL research related to ANY drug, and to make these studies a matter of public record... Then maybe we'd know what we're really risking every time we pop a prescription pill. Leading you AWAY from the slaughter, s II, MD Quote Link to comment Share on other sites More sharing options...
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