FDA ‘black-box’ warning – In 2003, the U.S. Food and Drug Administration began warning of an increased risk of suicidal thoughts among youths taking anti-depressants. In 2004, the agency required a new, more stringent label when antidepressants were prescribed to those under 18.
Between 2003-04 the youth suicide rate jumped 14 percent – the steepest increase ever seen – while the number of antidepressant prescriptions for youths dramatically dropped during the same period: 20 percent for children 10 and under, 12 percent for 11-to-14-year-olds and 10 percent for 15-to-19-year-olds.
What had started out as a voluntary admission quickly became involuntary. Joel arrived and we waited for an answer from the nurse who was already in the process of checking on my release. Soon we were told that the doctor had placed a 72-hour hold on me but that it wouldn’t start until Monday morning (this was Saturday) when he could see me. We couldn’t understand why the doctor wouldn’t release me when he hadn’t met me or talked to me.
There is an alarming connection between alcoholism and the various prescription drugs that increase serotonin. The most popular of those drugs are: PROZAC, ZOLOFT, PAXIL, LUVOX, SERZONE, EFFEXOR, ANAFRANIL, and the new diet pills, FEN-PHEN and REDUX. For seven years numerous reports have been made by reformed alcoholics (some for 15 years and longer) who are being “driven” to alcohol again after being prescribed one of these drugs. And many other patients who had no previous history of alcoholism have continued to report an “overwhelming compulsion” to drink while using these drugs.
The boy’s teachers recommended that he see a psychiatrist, who prescribed Zoloft, an antidepressant in the same chemical family as Prozac. The doctor said it would help Matt’s mood, make him feel better about himself. The boy started taking the pills and seemed to be in good spirits for a few days.
“The report shows that Glaxo [makers of Paxil] knew in 1989, long before Paxil was FDA approved, that people taking the drug were 8 times more likely to engage in suicidal behavior than people given a placebo, or sugar pill. Now, it stands to reason that even the most depressed person would decline to take Paxil if given these facts. Also, parents certainly would decline if they were told about the risks. . . . “The FDA approved Paxil on December 29, 1992, with no warning to doctors or patients of the significant increased risk of suicidal behavior,” he writes.