The end of February 2008 the truth came out about the initial studies done on these new antidepressants. These studies had never before been made public or even submitted to the FDA for their review. Yet these studies showed that the drugs were of no more benefit than a placebo! What the FDA does is judge the “Risk to Benefit” ratio for all drugs. Our question to them now is: “If this group of drugs are of no more benefit than a sugar pill and yet now have an FDA imposed Black Box Warning for increased risk of suicide – the next closest thing to banning a drug and they have warnings of suicide, hostility or psychosis with any abrupt change in dose, where is the Risk to Benefit ratio other than down the toilet? Why are they still on the market with little to no benefit and so great a risk?