 The Great Hall of the People, Tiananmen Square, Beijing, was the site for the opening ceremony for the latest FIP meeting.
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About a dozen years ago, a Nigerian member of the International Pharmaceutical Federation (FIP) made an impassioned plea for
the organization to take up the challenge of identifying and destroying the seamy world of counterfeit drugs. The call did
not fall on deaf ears. Since that time activities have been carried out in many areas of the globe.
This year's FIP meeting, held in Beijing, addressed the progress in identifying and dealing with issues related to ersatz
(or replacement) drug products. During a joint session of the FIP Board of Pharmaceutical Practice and the FIP Board of Pharmaceutical
Sciences, representatives from the United States, the United Kingdom, China, and India presented updates on the current status
of the problem.
World trade figures indicate that as much as 10% of drug products in the global market may be counterfeit. Statistics indicate
that India may have up to 35% of its products in question. However, the Indian government estimates that from 1995 to 2003,
the extent of the problem varied between 0.24% and 0.47% for counterfeit and from 8.9% to 10.64% for substandard drugs.
Model programPrafull Sheth, professional secretary, South East Asia Regional Forum, Delhi, reported on a model program to estimate the
extent of counterfeit medicines in India. Counterfeits include mimicking the full spectrum of innocuous to life-saving products.
The Indian government funded a survey to determine the extent of the problem.
A study was undertaken in 2003 to determine the relative prevalence by state/region, approximate the volume and percent through
retail outlets, and ascertain the prevalence in various therapeutic segments and cost ranges. It classed locations by degree
of the area's regulatory strength for the problem. A representative list of therapeutic categories and price variables was
used to determine the candidate drugs. "Mystery customers" were used to gather the samples, guides for physical verification
of samples were designed, and approved drug-testing laboratories were employed.
Sheth told the audience that the results of the survey may have been skewed to some degree by the methods used in sample gathering.
The study results showed an average extent of counterfeit drugs to be 3.1% based on physical inspection, and almost the same
degree was found in the areas regardless of strong or weak regulation. Lab values indicated only 0.3% did not meet pharmaceutical
standards. High on the list of questionable products were those for treatment of TB and certain antibiotics. The study did
not address products to be exported.
Big business
Reporting from the United States, Michael Anisfeld, pharmacy consultant, Globepharm, Deerfield, Ill., said drug counterfeiting
is big business. He quoted a figure of 8%-15% of global sales as counterfeit, with no continent immune. In a global market
worth $620 billion, those figures would project to $50-$93 billion. The Partnership for Safe Medicines projects $75 billion
worth of counterfeit drugs by 2010. While developing countries find counterfeits in drugs of need such as antimalarials, antibiotics,
and anti-HIV/AIDS drugs, the developed world sees more counterfeits in lifestyle drugs or the most costly products.
Noting the proliferation of Internet suppliers, Anisfeld said that approximately 70% of these products may be of questionable
provenence. He reminded attendees that more than 300 people had died in Panama in 2006 due to counterfeiting of glycerin by
the substitution of diethylene glycol from China. He tracked the movement of the product through wholesalers and brokers and
decried the lack of an auditing trail and the absence of sampling and analysis of the product before use.
Counterfeit packaging is a major problem, along with counterfeit holograms and counterfeit documentation.