War Profiteering
Anthrax, Drug Transnationals and TRIPs
Kavaljit Singh
Against the backdrop of September 11th terrorist attacks in the US, the current anthrax crisis has, once again, raised highly controversial issues related to intellectual property rights. Just a few months back, the world witnessed heated debate on the patent controversy when the Phar- maceutical Manufacturers’ Association of South Africa (PMASA), a body representing South African subsidiaries of 39 drug transnational corporations (TNCs), took the South African gov- ernment to court to prevent it from importing cheaper versions of patented drugs for patients suffering from Acquired Immuno Deficiency Syndrome (AIDS). However, under tremendous pressure generated by health activists and concerned groups around the world, the drug TNCs unconditionally dropped the lawsuit against the South African government.
No doubt, it is unfair to compare the AIDS pandemic in South Africa with the current anthrax crisis in the US. As compared to over 4.7 million patients suffering from AIDS and nearly 300 AIDS patients dying every day in South Africa, the anthrax crisis in the US has only affected a dozen people and claimed four lives till now. Yet there are several similarities. Not only both instances relate to public health, but more importantly, the bone of contention revolves around the Trade-Related Intellectual Property Rights (TRIPs) agreement of the World Trade Organi- Moreover, both these instances confirm the apprehensions of several developing countries as well as health activists that drug TNCs put profits before public health and the WTO regime severely restricts the capacity of national governments to take measures to safeguard public 1 Under compulsory licensing, a government can allow local companies to produce cheaper versions of drugs whosepatents are controlled by foreign drug companies. Local companies can produce and sell drugs in the country afterpaying a reasonable royalty on sales to the foreign drug companies. By increasing competition in the market, com-pulsory licensing can significantly lower the prices of drugs. While parallel importing allows countries to importcheap, generic versions of drugs without permission from the patent holders. For instance, the US government canimport drugs from an Indian company to sell them in the country. Since the prices of drugs are lower in severalcountries, particularly in the developing ones, parallel imports can help in lowering the prices of drugs. Recentexperience shows that both these measures can be helpful in promoting access to drugs at affordable prices. But thescope of using these measures is severely restricted under the present TRIPs regime.
The Price of Anthrax Drugs: Scarier than the Disease
The current controversy on patented drugs started when the first signs of anthrax attacks ap- peared in US in the early October 2001. Ciprofloxacin, an antibiotic drug, is prescribed for treating patients suffering from anthrax and other bacteria. German drug TNC, Bayer AG, holds the patent for Cipro (the brand name of ciprofloxacin) in the US till December 9, 2003. Under the present TRIPs agreement of the WTO regime, it implies that no other drug company is allowed to commercially manufacture and sell the generic versions of this drug in the US until the Bayer patent expires, except under extraordinary circumstances which allow compulsory licensing and parallel importing.1 Cipro is not only one of the best selling antibiotic drugs in the world but it is also a mega profit earning drug for Bayer. In US alone, Bayer sold $1.04 As the spectre of anthrax epidemic loomed large on the horizon, people started piling up stocks of Cipro. The sudden increase in the demand for Cipro led to a steep hike in its retail prices.
With the wholesale prices of Cipro at $4.67 for a 500 mg pill in the US, the retail prices went up to as much as $7 a pill. For anthrax treatment, it is recommended that patients should take two pills a day for 60 days. Thus, the retail price for two months stock of Cipro was well over $700, much beyond the means of poor Americans. Given the fact that two months stock of a generic version of Cipro costs a fraction of the prevalent price in the US, there was uproar over the Table 1: Selected International Prices of Ciprofloxacin
(Prices per pill of 500 mg in US dollars, October 2001) Bayer wholesale
Bayer federal government
Bayer government
Apotex generic/government
New Zealand
Bayer retail
South Africa
Bayer government
Polfa Grodzisk generic
Bayer retail
Blue Cross generic/retail
FDC generic/retail
Source: Compiled by author from several sources including Health Action International, Consumer Project Tech-nology and retail drug stores in Delhi.
monopolistic profits made by Bayer from the public health crisis. In India, for instance, Bayer’s Baycip (the brand name of ciprofloxacin in India) is available at drug stores at $0.13 a pill.
Thus, the retail price for two months stock of Baycip would be just $17. Whereas two months stock of a generic version of ciprofloxacin is available at a price as low as $8 at drug stores in In spite of higher prices, there were not adequate stocks of Cipro in the drug stores of the US.
Bayer expressed its inability to produce sufficient supply of Cipro at a short notice as requested by the US health authorities. At best, Bayer offered to produce 200 million pills within 60 days, much lower than the requirement of 1.2 billion pills. It would have taken several months for Bayer to meet the requirement. Confronted with a scenario where panic was spreading like wild fire all over the US, the Bush administration should have busted Bayer’s patent on ciprofloxacin and allowed sale of generic versions of the drug in the country. There are a host of drug compa- nies (including Ranbaxy, Dr Reddy’s Lab, and Cipla from India) which have already received quality approval from the US Food and Drug Administration for manufacturing ciprofloxacin.
Many of these companies were not only ready to provide ciprofloxacin to the US within 60 days, but more importantly, they offered it at a fraction of price than what Bayer was charging In fact, there are legal provisions in the US that allow compulsory licensing. Under the US Federal law (28 USC 1498), the US can purchase products like ciprofloxacin for official use from manufacturers other than the patent holder. In addition, the US government can also promulgate HR 1708 that exempts it from paying any compensation to Bayer for suspending its Not only the health activists and anti-corporate campaigners in the US, even politicians like Charles Schumer, a Democrat senator from New York, strongly demanded the suspension of Bayer’s patent. In a letter addressed to Tommy Thompson, US Secretary of Health and Human Services, Ralph Nader (consumer advocate and former presidential candidate) along with his colleague, James Love, called upon the administration to immediately authorize generic pro- duction of ciprofloxacin. In the letter, they pointedly asked the US Health Secretary, “your official responsibility is to protect the public’s health, and not to defend large profiteering phar- maceutical companies, which are already making a fortune because of our country’s current problems. How do you define the patriotic choice here?” Abject Surrender
Despite extensive domestic support to suspend Bayer’s patent on Cipro, the response of Bush administration was outrageous. Tommy Thompson considered it “illegal” to suspend Bayer’s patent on Cipro and he preferred to enter into negotiations with Bayer with the sole intention of lowering the price of Cipro. Facing an unprecedented public embarrassment, Bayer agreed to lower the price of Cipro for government purchase from $1.77 to $0.95.
Dubbed as “historic victory” in the US official circles, it would be absurd to view this agreement as a major accomplishment of the Bush administration. Rather, it was a major victory for Bayer because the agreement is based on the condition that the company would continue to remain the sole supplier of the drug in the US till December 2003. Further, the agreement with Bayer only covers government purchases of Cipro from the company while the drug will be sold at hospitals and drug stores at normal price. Even on discounted price, Bayer is still making prof- its from huge orders placed by the health authorities. Meanwhile, perturbed over this lopsided agreement with Bayer, consumer activists and concerned groups in several states have filed a lawsuit asking the court to scrap the agreement that gives monopoly rights to Bayer.
Had the Bush administration suspended Bayer’s patent and allowed the commercial manufac- ture and sale of generic versions of Cipro as per the existing national laws and international agreements, the real beneficiaries would have been the American people who would have pro- cured drugs in time and that too at reasonable prices. This episode confirms the allegations of anti-corporate activists that drug TNCs are being rewarded by the Bush administration for their large financial contributions to the Republicans in the election campaigns.
While these developments were taking place, allegations of price manipulations by Bayer have also come to light. It is alleged that the US subsidiary of Bayer AG signed illegal agreements with three of its competitors – Barr Laboratories, Rugby, and Hoechst-Marion Roussel – to prevent them from challenging its patent rights over Cipro. According to anti-corporate activists, Bayer has paid a total sum of $200 million till date to these companies for not manufacturing or marketing a generic version of Cipro, thereby neutralizing competition to protect monopoly Canada’s Flip-flop Posture
Watching these developments in the US from a close quarter, neighboring Canada announced on October 18 that it would suspend Bayer’s patent on Cipro and allow generic drug makers to manufacture and sell this drug in the country. The Canadian authorities also approached a domestic generic drug maker, Apotex, to produce one million pills as Bayer was unable to meet the requirement of Cipro. Apotex agreed to sell its generic version at $0.95 per pill to the health authorities, which was significantly lower than $1.59 charged by Bayer. This move by the Cana- dian health authorities sent shock waves in the entire pharmaceutical industry. The drug indus- try was taken aback by the sudden change in the Canadian stance because the country had been consistently supporting the US position on the intellectual property rights issue in the past.
Bayer in collusion with several lobby organizations used all kinds of pressure tactics, including threat to sue the Canadian government, for reversing this move. Within hours, the Canadian authorities reversed their stand and announced that they would honor Bayer’s patent on Cipro and would buy the drug only from the company. This sordid episode demonstrates the shady role played by the drug companies and their lobby organizations to stifle competition from low The US Administration: Hand in Glove with the Drug Giants
The Bush administration did not suspend the patent of Bayer largely because it was more con- cerned with the wider implications of such an action, particularly on the ongoing negotiations at the WTO. Realizing that scrapping Bayer’s patent would set a precedent that could give legiti- macy to the growing demands of the poor and developing world for more flexibility on patent issues, the US has given a clear message to the world that patents are more important than public health. Such a calculated move was not only meant to serve the corporate interests of drug TNCs, but it also conveyed the message to the developing nations that the US administra- tion would continue its discriminatory policy on the issue of patents.
It is ironical that the US administration abandons its responsibility when it comes to protecting its own citizens from public health calamities while it acts as a supercop when drug industry’s patents and profits are at stake. In international economic negotiations, the US administration has been one of the strongest allies of the global drug industry. Acting on the behest of drug TNCs, the US played a key role in initiating the Uruguay round of GATT negotiations where several agreements including TRIPs were pushed forward. The US has challenged various coun- tries at the WTO tribunal and has even threatened trade sanctions against several countries including Thailand, India, South Africa and Brazil for breaching TRIPs. Although TRIPs agree- ment does allow member countries to take compensatory measures to counter the effective monopolies of companies owning patents, but undue pressure has been put on many develop- ing countries to refrain from exercising their rights of compulsory licensing and parallel im- port. The dispute settlement case lodged by the US against Brazil in the WTO in relation to its Industrial Property Law and the lawsuit filed by 39 drug TNCs against the South African gov- ernment are some of the instances of pressure tactics.
Particularly in the last couple of years, US has been advocating imposition of stringent mea- sures for protecting patents under the so-called ‘TRIPs-Plus’ mechanism. Therefore, it is not surprising that the US has been vehemently opposing a document on patents and drug issues prepared by nearly 50 WTO member countries, including the Africa Group, Brazil, and India.
Concerned with poor peoples’ lack of access to affordable medicines due to high prices of pat- ented drugs and the resultant public health crisis, this document seeks suitable changes in the present TRIPs agreement. The document clearly states that “nothing in the [TRIPs] agreement shall prevent governments from taking measures to protect public health.” Lip Service at Doha Conference
The wider concerns for protecting public health were expected to usher substantial changes in the existing TRIPs agreement at the Fourth WTO Ministerial Conference in Doha, Qatar held during November 9-13, 2001. Not only health activists and NGOs, several poor and developing countries had also shown determination to raise this vital issue at the Doha conference. But the outcome of Doha conference was disastrous for the world’s poor because it provides a few concessions on drug patents issue. Except for providing least-developed countries additional 10 years to implement TRIPs and giving autonomy to governments to define public health emergencies in which TRIPs could be suspended, the Doha conference failed to resolve the fundamental conflicts between patents and public health. The lip service approach to this vital issue can be gauged from the fact that the declaration on the TRIPs agreement and public health was issued as a separate declaration, not part of the main Ministerial Declaration. With the key issues related to drug patents remain unresolved, the world is likely to witness patents versus poor patients conflicts in the coming years.
The agreement reached at Doha conference for a new round of negotiations is a significant achievement for the US, the EU and Japan as it opens up new opportunities for TNCs to further expand their global outreach. It is important to highlight the hypocritical stand of Indian au- thorities on WTO issues, which got completely exposed during the Doha Conference. A few weeks before the Doha conference, Indian authorities took a strong posture seeking drastic changes in the TRIPs agreement as well as opposing new round of negotiations till contentious issues related to the implementation of Uruguay round of negotiations are resolved. Not only the poor and developing countries, several Indian and international NGOs also joined the ranks in support of Indian authorities. But within hours after asserting that “a new round of trade talks at the WTO is not necessary, it is evil,” India’s Commerce Minister, Murasoli Maran, agreed to a new round of formal negotiations without any major gains in key areas such as textiles, agriculture, TRIPs and transfer of technology. This is hardly surprising given the fact that the same Indian government is not just pursuing amendments in the domestic patent laws to conform with the WTO regime but also pushing liberalization agenda in several sectors of economy (for instance, financial sector) that are well beyond the purview of WTO.
Wider Ramifications
Several inferences can be drawn from the anthrax crisis in the US. First, by sacrificing the public health concern of its own citizens to protect private interests of drug TNCs, the US has un- abashedly acknowledged the supremacy of patents over public health. Second, the present patent regime not only poses a grave danger to public health in the poor and the developing world, even the developed world is also not immune to it. Hence, this episode should serve as a wake up call to the rest of the developed countries who usually follow the footsteps of the US on patent issues. Poor and ordinary people, whether they live in New York or New Delhi, have a basic right to sound health, and therefore, safeguarding public health must take precedence over patents and monopoly profits of the drug TNCs.
Third, apart from universal health programs and other public funded interventions, it is of utmost importance that monopolies in the drug industry be dismantled to ensure that crucial drugs are made accessible to the poor patients at affordable prices. Therefore, strict regulation of drug TNCs must be an integral component of building public health system in the developed Fourth, with critical support from the developed countries not forthcoming, the responsibility for demanding a comprehensive review of TRIPs, including reduction in the duration and scope of patent protection for drugs that are essential for public health rests with the poor and devel- oping countries. This calls for greater unity and solidarity among the poor and the developed world on issues of common interest at the WTO and other international economic negotia- Finally, it is high time that the primacy of national health policy over international agreements,


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