Legal but deadly

Article Highlights

  • A different kind of #drugwar: In emerging markets, more than 4% of legal medicines fail quality tests

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  • Cheap medicines only benefit patients if effective: some generic manufacturers aren’t up to par

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  • Western purchasers of #Chinese medicines should pressure regulation authorities for better tests on #medicine quality

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Patients in emerging markets want greater access to medicines, but supplying medicines cheaply is proving problematic. Part of the difficulty is the proliferation of illegal counterfeits in the poorest markets. Yet our new research shows that substandard medicines—those legally but poorly produced—pose an equally dangerous threat to patients1. Without a strong commitment from pharmaceutical companies and drug regulators around the globe, the problem will worsen.

The demand for medicines from the growing middle class in India, China, and, more recently, Africa is creating opportunities for pharmaceutical companies. McKinsey projects that by 2025 China and India will be respectively the third- and fifth-largest consumers in the world. African households with discretionary spending are also set to increase by 50 percent over the next ten years. These trends are significant for major Western companies like Bayer and Novartis, who already generate 25 percent of their revenue from emerging markets, up from single-digit percentages only a decade ago.

Roger Bate is the Legatum Fellow in Global Prosperity, and Julissa Milligan is a research assistant at AEI.

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About the Author

 

Roger
Bate
  • Roger Bate is an economist who researches international health policy, with a particular focus on tropical disease and substandard and counterfeit medicines. He also writes on general development policy in Asia and Africa. He writes regularly for AEI's Health Policy Outlook.
  • Phone: 202-828-6029
    Email: rbate@aei.org
  • Assistant Info

    Name: Katherine Earle
    Phone: (202) 862-5872
    Email: katherine.earle@aei.org

 

Julissa
Milligan

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