Access to medicines refers to the reasonable ability for people to get needed medicines required to achieve health. Such access is deemed to be part of the right to health as supported by international law since 1946.
The World Health Organization states that essential medicines should be available, of good quality, and accessible. Reasonable access to medicines can be in conflict with intellectual property and free markets. In the developing world people may not get treatment for conditions like HIV/AIDS.
The World Health Organization states that essential medicines should be available, of good quality, and accessible. Reasonable access to medicines can be in conflict with intellectual property and free markets. In the developing world people may not get treatment for conditions like HIV/AIDS.
Hindrances to access
Most hindrances to access revolve around market competition and lack of it.
Patent protection and exclusivity
Patents provide an owner exclusive rights
to a product or process for 20 years in a particular territory. The
owner of the patent has the right to prevent the manufacture, use, sell,
import, or distribution of the patented product. It is argued that patent protection allows pharmaceutical companies a monopoly on particular drugs and processes.
Data exclusivity
Data exclusivity is a regulatory measure limiting the use of clinical trial data and provides conductor of the trial temporary exclusive rights to the data. Many suggest that extending exclusivity periods can have consequences in delivering medication, especially generic brands, to developing countries. However, extending patent terms can be reinvested for research and development and/or a source of funding for drug donations to low-income countries. Others suggest that data exclusivity works to diminish the availability of generic drugs.
Many argue that pharmaceutical companies push for data
exclusivity—seeking to extend their monopolies by advocating for market
exclusivity provided by patents and data exclusivity, or protection for
new medicine.
Cost
In some countries pharmaceutical company have ultimate control of the
pricing of their patented product. Therefore, the owner has control of
the pricing of the medication, based on the price level the owner deems
best to reflects their ability to manufacture and the level of profit
desired. Purchasers have little say over the price set. It is argued that competition is necessary to lower drug prices and improve access to affordable medications.
Price gouging
is defined as the excessive increase in prices by sellers of essential
goods to a level deemed higher than reasonable or fair. This sharp
increase in prices may leave the buyer vulnerable. It also leads to
inequitable access to essential goods among different socioeconomic
groups.
It is argued that pharmaceutical companies have dramatically increased
prices for treatments that are essential in treating diseases such as HIV/AIDS, hepatitis C, and cancer.
Lack of Generic Brands
Many
argue that generic brand production in developing countries increases
competition and therefore is essential to bridge the global drug gap.
As argued by various sources, the push for more measures such as market
and data exclusivity, hinders low-income countries' ability to
manufacture and produce generic drugs. However, low-income countries often lack the essential infrastructure to allow for generic brand production.
In order the use of the medication to be effective, it must be
manufactured in optimal laboratory conditions. Developing countries
often lack air conditioning, stable electrical power, or refrigerators
to store samples and chemicals.
Also, quality generic brand production is limited by a government's
ability to create effective spaces of market competition and to monitor
the quality of generics brands; this ability has been found to be
limited in certain developing countries. It also argued that international aid,
state investment, and measures for infection prevention are necessary
to allow for generic brand production in low-income countries.
Legislation
Trips agreement
The Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS), is a multilateral agreement between all member nations of the World Trade Organization (WTO), effective January 1995. This agreement introduced global standards for enforcing and protecting nearly all forms of intellectual property rights
(IPR), including those for patents and data protection. Under the TRIPS
Agreement, WTO member nations, with a few exceptions, are required to
adjust their laws to the minimum standards of IPR protection. Member
nations are also obligated to follow specific enforcement guidelines, remedies, and dispute resolution procedures. Before TRIPS, other international conventions and laws did not specify minimum standards for intellectual property laws in the international trading system. The TRIPS Agreement is argued to have the greatest effect on the pharmaceutical industry and access to medicines.
It is argued that the TRIPS agreement negatively impacted generic drug
industries in countries such as India. However, others argue that the
agreement is open to interpretation. A clause in the TRIPS agreement
allows compulsory licensing,
which permits the manufacture of generic brands of patented drugs, at
prices set in a competitive market in cases of national emergencies. For example, many believe that the HIV/AIDs crisis in Africa and South East Asia
and the inadequate access to essential AIDs medications constitute a
national emergency. Therefore, the TRIPS Agreement can be interpreted to
allow the manufacture of generic brands of patented HIV/AIDs drugs.
Doha Declaration
Further legislation such as Doha Declaration of 2001 worked to rectify the negative impact of the TRIPS Agreement. The Doha Declaration on the TRIPS Agreement and Public Health, effective November 2001, was adopted by WTO Ministerial Conference of 2001.
Many argued that the TRIPS Agreement hindered developing countries from
implementing measures to improve access to affordable medicines,
especially for diseases of public health concern, such as HIV, tuberculosis, and malaria.
The Doha Declaration responds to concerns of developing countries that
patent protection rules and other IPRs were hindering access to
affordable medicines for populations in those countries.
The Doha Declaration emphasizes the flexibility of the TRIPS Agreement
and highlights the right of respective government to interpret the TRIPS
Agreement in terms of public health. It refers to specific parts of
TRIPS, such as the use of compulsory licensing for pharmaceutical drugs
only in the case of a national emergency and circumstances of extreme
urgency and the right to determine what constitutes this—such as to
address public health issues.
Paragraph 6 System
The
declaration also allows for countries without manufacturing
capabilities to turn to another country for the export of generic brands
of patented medicines. This is known as the paragraph 6 system.
As of 2010 it had only been called upon once, concerning the export of
medicines from Canada to Rwanda, with varying opinions about its results
and potential.
Differences by geography
Africa
There is estimated to be more than 4 million HIV infected individuals in South Africa. Out of this, only 10,000 individuals are able to afford access to essential AIDS medications at their current prices. In Malawi, out of one million infected individuals, 30 have access to life-sustaining essential AIDS medications. In Uganda, out of the estimated 820,000 infected individuals, only about 1.2% can afford essential AIDS medications.
Latin America
There is estimated to be 1.8 million individuals HIV infected individuals in the Latin American region. Brazil is argued to be one of the most affected by the AIDS epidemic. There is also a high prevalence of HIV in smaller countries such as Guatemala, Honduras, and Belize.
However, Brazil is argued not to have restrictive patent laws. In the
mid 1990s, Brazil began manufacturing generic brands of vital AIDS
medication. Due to this, Brazil's AIDS mortality rate declined by almost
50%.
India
Many Indian families live below the poverty line due to healthcare expenses. From 1972 to 2005, due to a lack of patent laws
for drugs in India, Indian drug companies were able to use alternative,
legal processes to manufacture generic versions of drugs. These generic
drug companies were able to produce low-priced drugs that were
considered among the lowest in the world. This allowed India to provide
free antiretroviral treatment to 340,000 HIV infected individuals in the
country. Majority of adult antiretroviral drugs purchased for
donor-funded programs in developing countries were supplied by Indian
generic drug companies. In compliance to the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS), India reintroduced patent laws for drugs in 2015.
Differences by sector
Vaccines
The majority of deaths from vaccine-preventable diseases occur in low and middle income countries. In low-income countries, more than 90% of deaths are from pneumococcal disease, 95% from Hib, and 80% from hepatitis B. Although widely used by high-income countries, in 2006, Hib vaccine usage in Africa was about 24% In the Americas, Hepatitis B vaccine usage was at 90%. In Southeast Asia, where there is hepatitis B epidemic, the Hib vaccine coverage was only 28%. The human papillomavirus (HPV) vaccine is considered the most expensive vaccine in history. However, the majority of those that suffer from cervical cancer are in developing countries.
Epidemics and access
HIV/AIDs
The appearance of generic manufacturers in low-income countries, such as India and Brazil, was key to increasing access to HIV/AIDS treatment in low- and middle- income countries (LMICs). Due to the introduction of generic brand competition, first-line antiretroviral drugs' prices dropped by more than 99%, from $10,000/year per patient in 2000 to less than $70 in 2014.
Daraprim
On August 10, 2015, Turig Pharmaceuticals, a pharmaceutical company owned by Martin Shkreli, purchased the rights to a Daraprim. Daraprim, an anti-parasitic and anti-malarial
drug, is considered an essential drug for HIV treatments. It is widely
used to treat patients with AIDS-related and AIDs-unrelated toxoplasmosis.
At the time, no other generic versions of the drug was available. Turig
dramatically raised the price of the drug from $13.50 a tablet to $750,
a 5000% increase.
Campaigns
A number of countries and organizations have efforts to improve access to medicines in specific areas of the world.
The Canada's Access to Medicines Regime allows developing countries to bring in medicines at lower cost.
It specifically allows companies in Canada who may not own the right to
make a medication to do so for export to certain countries in the
developing world.
Médecins Sans Frontières has had such a campaign since 1999 known as the Campaign for Access to Essential Medicines.
In Tanzania,
the Ministry of Health and the Tanzania Food and Drugs Authority and
the Strategies for Enhancing Access to Medicines Program introduced
accredited drug dispensing outlets, with aid from Bill & Melinda Gates Foundation. It worked to create a nationwide chain of dispensers, which provide quality pharmaceutical drugs and services to its citizens.
Gavi, the Vaccine Alliance is an international public-private partnership, created in 2000, devoted to improving access to vaccines in low-income countries.
The organization partners with several developing countries, donor
governments, research agencies, and vaccines companies in both in
industrialized and developing countries. It also partners with
organizations such as the World Health Organization, UNICEF, the World Bank, the Bill & Melinda Gates Foundation and other private philanthropists.
Gavi is noted as an important source of external funding for vaccines
in low-income countries and played a crucial role in introducing the HPV
vaccine and other new vaccines to developing countries.
In Kenya,
the Kenya Coalition for Access to Essential Medicines (KCAEM), was
formed in response to Kenya's Industrial Property Act 2001. The act
outlined the rights of patent holders. Members of this coalition are
local community-based and national NGOs, international NGOs, healthcare
providers, journalists, lawyers and other individuals. The coalition
works primarily with people living with HIV/AIDS and access to essential
HIV/AIDS medications and treatments.
It urges for flexibility in interpreting the TRIPS Agreement and
efforts to implement production of generic antiretroviral drugs by local
manufacturers and/or to import inexpensive drugs. It also calls for pharmaceutical companies to reduce the price of their medications.
The coalition has garnered support from key government officials and
organizations such as Kenyan Property Institute, Kenyan Ministry of
Trade, and the Minister of Trade Mr. Nicholas Biwott MP.