Study Finds FDA Rx Actions Suspicious

Author: Lawson Health Care Foundation
Dateline: Wed, 16 Mar 2005

freeNewsArticles Story Summary: “LOS ANGELES, Calif. /Send2Press Newswire/ -- Dr. Gary Lawson announced the results of a two-year study showing that the large sums of money paid yearly to the Food and Drug Administration (FDA) by the brand name pharmaceutical manufacturers gives the drug industry financial leverage and influence over the FDA. The study concluded that until the drug industry money or the strings attached to the money are eliminated, U.S. citizens should be extremely cautious and highly suspicious of FDA actions related to prescription drugs.”



A R T I C L E:

LOS ANGELES, Calif. /Send2Press Newswire/ -- Dr. Gary Lawson announced the results of a two-year study showing that the large sums of money paid yearly to the Food and Drug Administration (FDA) by the brand name pharmaceutical manufacturers gives the drug industry financial leverage and influence over the FDA. The study concluded that until the drug industry money or the strings attached to the money are eliminated, U.S. citizens should be extremely cautious and highly suspicious of FDA actions related to prescription drugs.

In 1992, to speed up new drug approvals and eliminate a backlog of needed life-saving medications, Congress authorized the collection of drug industry fees for one five-year period. Although no new drug approval efficiencies were realized after year five, the law was extended twice. According to the ULV study, with each extension, the drug industry paid significantly higher fees, and then, used the higher fees as leverage to limit the FDA's ability to act as an objective consumer protection agency.

As the brand name drug industry acquired more financial leverage over the FDA, the ULV study showed that adverse drug reaction reports more than doubled. Americans have a 32% higher chance of experiencing a reportable adverse drug reaction. More deadly drugs were released in the U.S. first and stayed on the U.S. market longer. The costs of drugs to consumers skyrocketed. The FDA shifted its policy to protect the drug industry's U.S. monopoly, and actively worked toward stopping the flow of lower cost Canadian medications.

Off-label drug promotion was authorized. Direct to consumer advertising was authorized. The FDA significantly decreased other consumer protection services, and the FDA allowed the drug industry to set internal Agency objectives, goals, and FDA job descriptions.

For more information see www.FDAStudy.com.

###


Copyright © 2005 by Lawson Health Care Foundation and Send2Press® Newswire, a service of Neotrope® - all rights reserved. Information believed accurate but not guaranteed. Sourced on: freeNewsArticles.com.

Story Title: Study Finds FDA Rx Actions Suspicious
• REFERENCE KEYWORDS/TERMS: , , , , Health, Diet and Fitness, , , .

IMPORTANT NOTICE: some content which is considered "old" or "archival" may reference an event which has already occurred; some content possibly considered "advertorial" may also reference a promotion or time-limited/sensitive offering, and in all of these instances certain material may no longer be valid. For notably stale content, you should directly contact the company/person mentioned in the text (Lawson Health Care Foundation); this site cannot assist you with information about products/services mentioned in the news article, nor handle any complaints or other issues related to any person/company mentioned or promoted in the above text. Information believed accurate but not guaranteed as of original date of story [Wed, 16 Mar 2005 16:42:00 GMT].

USE THIS CONTENT FOR FREE: To use this content in your newspaper, broadcast outlet, news portal, blog/ezine or similar, free of cost, CLICK HERE to learn how.