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What America Does to its Children
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Pfizer Behind Closed Doors
Pfizer and Research Misconduct in Zoloft Clinical Trials
Research misconduct (scientific fraud) is the violation of the standard codes of scholarly conduct and ethics in scientific research. It includes all forms of intentional distortion of the research process or reckless disregard of that process that place the scientific record at risk. It also includes the violation of informed consent, and improper use of information derived from the assumption of risk by other humans.
In one 1983 document Pfizer reported that a patient had been taken off Zoloft (an antidepressant) during a clinical trial. The portion of the report that had been in the public domain (and presumably also with the FDA) from 1983 to 2004 indicated only that the patient was taken off the drug because of “treatment failure and nausea, anorexia and painful urination.”
However this explanation differs with the true clinical trial record which indicates that the patient had been withdrawn at day 11 of the trial because of thoughts of killing himself and others : “[The patient] began to verbalize feelings of killing other people and then himself.”
This link will take you to Scientific Misconduct where you can view the actual copy of a of this document.
The Pfizer Manual ; How to Discredit the Truth
When a case comes before the court of an Involuntary Adverse Reaction Event known as (Involuntary Intoxication), Pfizer has made sure by creating the how to discredit the experts by producing the Pfizer Manual.The manual is based off one important subject , No clinical data available on the association between homicide and SSRI medication.
The reason for this is because Pfizer will not conduct any clinical trials on that issue, hince as long as they have no association to homicide and SSRI's, the Pfizer Manual and Pfizers own lawyers get involved and distrubute the manual to presecutors in cases which involve the claim of an Involuntary Adverse Reaction Event.
Please view partial listing of Victims of Antidepressant Reactions
The FDA (The Food and Drug Adminstration ), What role do they now play in the Public's safety ?
As of date the FDA has failed to take any action into the SSRI homicidial Ideation/association issue, giving the American public the impression that the FDA can not or will not act on this danger to our children.
The FDA must remember whose interests it is supposed to protect and to issue a warning of a possible risk of harm to others on all SSRI medication guide inserts which will protect our children. I hope when looking at this issue the FDA would rather err on the side of our children’s safety and their Lives.
Big Pharma for years has known about the dangers SSRI medication can pose to some, in a 1994 dated memo email made public from a criminal trial involving an adverse reaction (Involuntary intoxication), from Roger Lane M.D.
Quote:
Marketing is very aware that a patient on Zoloft involved in an incident of mass homicide could severely affect the image and commercial success of Zoloft.
READ THE FULL EMAIL HERE