It goes without saying that no government
can allow market forces a free hand in the pricing of medicines. Affordability
of medicines has to be ensured so that no person in need of it has to suffer.
This is especially true in India where a large number of people are still poor.
The Narendra Modi government has been focusing on making medicines affordable
by making them available through Jan Aushadhi Kendras, enabling price control
of essential medicines, promoting prescription of generic medicines by medical
practitioners and focussing on a conducive intellectual property regime (IPR).
Generic drugs
Generic drugs tend to
cost less than branded ones. These drugs form the largest segment of the Indian
pharmaceutical sector. The increasing prevalence of chronic diseases and
ever-rising costs of hospitalisation and medicines are responsible for the
growth of the generic drugs market. In this context, the National Health
Protection Scheme (NHPS), also known as ‘Ayushman Bharat’, launched in 2018 —
which seeks to insure 10 crore families for ₹5,00,000 — is expected to
exponentially increase the demand for medicines. A well-functioning, end-to-end
generic medicine supply chain will keep costs low.
Targeted
implementation
An initiative to ensure affordable medicines through dedicated
outlets was launched in the form of the Pradhan Mantri Bhartiya Janaushadhi
Pariyojana (PMBJP) in 2008. The mission was to create awareness among the
public about generic medicines and provide commonly used generic medicines and
health-care products. However, as on March 31, 2012, only 157 stores were
opened; later, many became non-functional. Till the end of 2014-15, there were
99 stores.
In 2014, the impetus came from the Modi government.A ‘Strategic
Action Plan’ was prepared. The product basket now has more than 600 medicines
and 154 surgical and consumables in all therapeutic categories. There are over
4,000 Jan Aushadhi Kendras in the country. These centres are gradually becoming
ubiquitous and government-procured generic medicines are sold at prices that
are between 50% and 90% cheaper than the branded medicines in the open market.
Directive on
prescriptions
Due to sustained efforts by the government to put in place a
legal framework to promote generic medicines, the Medical Council of India
issued a directive in September 2016, making it mandatory — by amending the
Indian Medical Council (Professional Conduct, Etiquette and Ethics)
Regulations, 2002 — to prominently mention the generic names of drugs along
with brand names in prescriptions. There is an advisory to State drug
controllers that all branded drugs, imported or domestically manufactured,
should mandatorily have generic names mentioned in bold letters while
packaging.
The instrument of price control is also being used to restraint
companies from pricing their medicines exorbitantly. ‘Every few years, the
Health Ministry, in consultation with experts, draws up a National List of
Essential Medicines (NLEM). These medicines, deemed essential for the treatment
of common conditions, automatically come under price control. Under NLEM 2015,
a total of 376 drugs are under price control. In addition, the government has
the power to bring any item of medical necessity under price control —
paragraph 19 of the Drugs (Prices Control) Order, 2013. This provision was used
to regulate the prices of cardiac stents and knee implants’. There has been an
attempt by the government to strike a fine balance between the health interests
of consumers and the financial health of Indian pharmaceutical companies.
India has also emerged as the low-cost supplier of medicines to
other countries and is the largest provider of generic medicines globally in
terms of volume. The Indian pharmaceutical sector industry supplies over 50%
per cent of the global demand for various vaccines, 40% of generic demand in
the U.S. and 25% of all medicines in the U.K. At present, over 80% of
antiretroviral drugs (used globally to combat AIDS) are supplied by Indian
pharmaceutical firms.
A serious threat to affordability of medicines comes from big
global firms. These pharmaceutical companies and their governments have been
trying to lobby with the Indian government to make patent protection more
stringent despite the fact that both compulsory licensing and prohibition of
evergreening, provided under the Indian Patents Act, 1970, are valid under the
TRIPS agreement of the World Trade Organisation. India has resisted any change
in its intellectual property laws that can have the effect of making medicines
unaffordable.
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