AHRP has received an appeal for help to prevent the firing of courageous, honest FDA scientists who risked their careers to save lives by informing Congress about serious safety concerns involving dangerous, FDA-approved drugs and medical devices.
FDA employees should not be afraid to speak honestly and freely about misconduct that threatens the health and safety of all Americans.
Take Action by sending a message to Margaret Hamburg, FDA Commissioner.
See suggested text at: http://www.capwiz.com/whistleblowers/issues/alert/?alertid=22364531&type=ml
Alliance for Human Research Protection
A Catalyst for Debate
www.ahrp.org
Prescription drugs for allergies, arthritis, diabetes and
other ailments kill some 200,000 Americans every year, and put another 8.8
million in the hospital. This means that only cancer and heart disease kill
more patients than drugs.
The safety hazards posed by FDA-approved defective drugs
and medical devices are documented in an ever growing number of criminal and
civil lawsuits against manufacturers. The latest case (aired on CBS 60 Minutes)
involved a drug company whistleblower whose documented investigation of a GSK
manufacturing plant--following a slip shod FDA investigation-- resulted in
GlaxoSmithKline pleading guilty to criminal marketing of drugs it knew to
adulterated: the antidepressant, Paxil CR, the diabetes drug, Avandia, a cancer
drug, Kytril, and Bactroban." The
company was convicted and ordered to pay $750 million in settlement. http://www.cbsnews.com/stories/2010/12/29/60minutes/main7195247_page4.shtml
GSK has spent $3.4 billion in legal costs related to
Avandia lawsuits in the fourth quarter of 2011. This drug was pulled from the
European market by the EU Medicines Agency which determined the risks outweigh
any benefit. Yet, the FDA allows its continued marketing in the U.S.
The FDA has a well-known track record of retaliating
against employees who step up and raise concerns. Instead of intimidating its
conscientious scientists, the FDA must protect and encourage its employees to
report any misconduct they witness that threatens the public health. I strongly request that you do not fire
dedicated FDA scientists who report managerial misconduct to Congress and the
American people.
FDA managers, concerned with pleasing industry through
fast approvals, have pushed to approval medical devices that lead to
unnecessary risks, cancers, and even death. Many FDA scientists, appalled by
the fast-tracking of these approvals, have tried to report the misconduct to
Congress and the President. Their reward? . . . a hostile work environment and
termination.
The most recent FDA notice of proposed removal is of a
23-year veteran medical doctor and PHD scientist for alleged misconduct.
Reason? . . . nine emails sent to her Congressional liaison in an effort to
report FDA misconduct to Congress. Positively chilling!
Are we living in a totalitarian state? We need more not
less WikiLeaks to disclose the underhanded behavior of government officials in
their handling of the nation's business--especially medical practice which is
literally a matter of life and death.
The first and most immediate step to take is to
immediately rescind the letter of proposed removal of the 23-year veteran
scientist (EEO Case # FDACDRH02410).
Do not fire this American hero. Reward her.
Vera Hassner Sharav
President
Alliance for Human Research Protection
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