(Natural News) Robin Feldman, a professor in pharmaceutical law at University of California, testified in September 2016 before the House of Representatives judiciary subcommittee about the state of the opioid addiction in the United States, saying that even though “open and vigorous competition is the backbone of U.S. markets…we are not seeing that in the market for addiction medicine.”
This is because, according to Feldman, big pharmaceutical companies hold a monopoly over the manufacture and release of major commercial drugs.
Statistics show that the percentage of people in America that perish due to drug overdoses has quadrupled since the late 1990s; drug overdoses are now ranked as the leading cause of death for Americans under 50 years old.
Feldman and her colleagues studied the filing of petitions at the Food and Drug Administration (FDA) in their book Drug Wars: How Big Pharma Raises Prices and Keeps Generics off the Market.
“Some of the petitions were just stunning to us. For example, some petitions soberly ask the FDA to require, well, what it already requires, such as ensuring that the generic drug product is stable and has an appropriate shelf life. Other petitions tie the application up in knots for reasons that are hard, even for the FDA, to discuss with a straight face,” Feldman noted.
For instance, the manufacturer of the blood pressure medicine Plendil asked the FDA to delay approval of the generics by saying they are concerned over how different types of oranges in orange juice might affect absorption of the medication and demanding additional data on the juices that are used during clinical trials.
Pharmaceutical companies employ a tactic to modify the dosage or modulation of a drug whose patent is about to expire, allowing them to stamp a brand-new set of patents on their “new and improved” version of the drug. (Click to Site)