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AHRP Press Briefing: Antidepressants and Suicide-Related Risks for Children |
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Tuesday, 14 September 2004 |
Scientists' Presentations at AHRP Press Briefing in Conjunction
with FDA Hearings:
- Peter Mansfield, MD, University of Adelaide (Australia), Director
of Healthy Skepticism discussed the illusion of potency in light of
the meta-analyses in the British Medical Journal (which he co-authored)
and the Lancet.
Dr. Mansfield's power point presentation
- Peter Breggin, MD, a psychiatrist with a sub-specialty in clinical
psychopharmacology, who was among the first to recognize adverse antidepressant
drug reactions
Dr. Breggin's presentation
- Lawrence Diller, MD, a pediatrician and family therapist who has
evaluated and treated more than 2,500 children
Dr. Diller's presentation
- Stefan Kruszewski, MD, a clinical and academic psychiatrist, and
Associate Medical Director of Physicians' Health Programs, Pennsylvania
Medical Society
Dr. Kruszewski's presentation
- David Healy, MD, Director of the North Wales Department of Psychological
Medicine and Visiting Professor, University of Toronto,
who in large
measure has brought pressure to bear on the FDA to examine the pediatric
data. Dr Healy shed light on FDA's asymmetric standards for evaluating
efficacy and safety, and presented newly uncovered documents.
Dr. Healy's power point
presentation
Accompanying text for Dr. Healy's
power point slides
Appendix - Brecher Document
(140 K pdf)
AHRP's September 14, 2004 press
statement re the FDA & concealment of suicide-related risks of
antidepressants
AHRP's testimony
submitted to the FDA Psychopharmacological Drugs Advisory Committee and
Pediatric Subcommittee Drugs Advisory Committee at the September 13-14,
2004 Meeting RE: Suicidality Associated with Antidepressant Drug Treatment
AHRP's press release announcing
AHRP's September 14 press briefing
David Healy's response
(502K pdf file) to a slanderous personal attack by Pfizer, posted by
the FDA on FDA's website, August 20
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