Inside the World of Counterfeit Drugs

Part 2: The European Repackaging Debate – Last week we witnessed the confusing practice of repackaging of prescription medicines within the European Union (EU) through the eyes of a fictitious Dutch patient picking up his blood pressure tablets at a city retail pharmacy. The patient’s experience is shared by millions of Europeans living in Germany, Great Britain, and Holland among other countries. Under current EU rules, medicines can be re-boxed or re-labeled after they leave the site of production, and tablets can be removed from their blisters and reconditioned. Counterfeiters can exploit this fact in order to sneak their fake goods past regulators. One of the prime sources of counterfeit medicines, which can enter the drug supply at the point of repackaging, is the Internet.

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Dangerous Assumptions Drawn From List of Permitted Countries

Periodically proposals are floated both in Washington, DC and state capitols that would allow Americans to import drugs from 32 “permitted” countries – Australia, Canada, Japan, New Zealand, Switzerland and the 27 members of the European Union. There is a perception that these countries have “safe” drug supplies insulated from the dangers that every other nation in the world.

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Letter to President Barack Obama

April 8, 2009 President Barack Obama1600 Pennsylvania Avenue, NWWashington, DC 20500 Dear Mr. President, On behalf of the Partnership for Safe Medicines (PSM), a group of organizations and individuals that have policies, procedures, or programs to protect consumers from counterfeit or contraband medicines and dedicated to the safety of the drug supply, I would like…

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Drug Importation: Small Savings at a Large Cost

Supporters of drug importation like to cite the statistic that if the United States were to permit drug importation, it would reduce total drug spending by $40 billion over 10 years. This figure is from the 2004 Congressional Budget Office (CBO) issue brief on drug importation.

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The Last Line of Defense Against Counterfeit Drugs

Recently, there has been talk in our nation’s Capitol about overhauling the Food and Drug Administration’s (FDA) presence both in the United States and abroad. This is an important step in improving the safety of prescription medications from the global public health threat of counterfeit drugs and the untold harm they cause unsuspecting consumers. But, with limited budget and resources, will the FDA be able to pull off the task?

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