Congress Barbecues FDA part 1

The FDA and Risperdal go back to at least 12/29/93
The latest approved label (approved 08/14/2008) is not available on this site for RISPERDAL, NDA no. 020272

The FDA and Zyprexa go back to at least 09/30/96
The latest approved label (approved 08/14/2008) is not available on this site for ZYPREXA, NDA no. 020592

There's a lot of "Label is Not Available" on FDA's site. On an annual budget of $2.2 Billion FDA can damn well afford to Make it available on site: Their site, which Everybody Else, is Paying for.

It's now 12 & 15 years down the "Investigative" road and only Now have the Investigators Finally copped to the fact that the newer - Vastly More Expensive Atypical Antipsychotic Poisons - are Worse, ..... In Children, ..... than the older Typical Antipsychotic Poisons.

See AHRP. & Bloomberg.

And it took these Investigating Ideates 15 years to gum shoe this? While they were Taking The Money, ..... From the Manufacturers of these Atypical Antipsychotics, ..... to conduct their Investigations of "Disorders" which Their fellow Psychiatrists voted into Money Makers, by a Show of Hands?

Where is the self proclaimed "trusted, independent, efficient gatekeeper it is now" FDA on this, ..... Today?







Why, would the FDA - NOW that the Floodgates of Naked Eye SCIENCE & NOT Psychiatry's Bull S**T Ideations, are opening Against those manufacturers - want to Preempt Your Right to Sue those manufacturers, ..... who Grease this FDA with a Half $ Billion a year"?





What might be the Real purpose of FDA labels, ..... when you can even Find the label ..... of FDA labels like this one?

10:06:2006 pg. 13

"The risk of developing tardive dyskinesia and the likelihood that it will become irreversible are believed to increase as the duration of treatment and the total cumulative dose of antipsychotic drugs administered to the patient increase. However, the syndrome can develop, although much less commonly, after relatively brief treatment periods at low doses.

There is no known treatment for established cases of tardive dyskinesia, although the syndrome may remit, partially or completely, if antipsychotic treatment is withdrawn. Antipsychotic treatment, itself, however, may suppress (or partially suppress) the signs and symptoms of the syndrome and thereby may possibly mask the underlying process. The effect that symptomatic suppression has upon the long-term course of the syndrome is unknown."


In "Regular English": the product causes tardive dyskenisia - which is brain and CNS damage - and the Psychiatrists who Cause tardive dyskenisia, "Treat" the Agony They Directly Caused, FOR MONEY, by Poisoning the Victim with even More of the Product to cover up their Opinionated skullduggery.

Read the FDA document. It speaks of 6-8 week trials, and the Long term Effects are "unknown", in Trade for a Half $ Billion a year.

Maybe FDA was too busy counting up that DRUG MONEY to find out what the Long Term Effects were, in between labels informing us that "efficacy and safety were established" in 417 Children aged 13-17, ..... only 3 pages After admitting that cardiopulmonary arrest and sudden death were "temporally, ..... but not necessarily causally related" to use of the product.

So just What Have these FDA-ocrats been doing for 15 years?



The last video is obviously a satire, ..... or is it?

And make sure to include a fork. We wouldn't want the FDA to burn itself on those Half $ Billion Dollar Pies.

Thanks again to Hissey Kientz LLP, Congressmen Waxman and Braley, and of course, the Onion.