# \[e-drug\] Pneumonia vaccine

**URL:** <https://talk.edrugplus.org/t/e-drug-pneumonia-vaccine/30549>\
**Category:** e-drug\
**Created:** [September 20, 2008, 4:08pm UTC](https://talk.edrugplus.org/t/e-drug-pneumonia-vaccine/30549 "2008-09-20T16:08:00Z")\
**Posts on this page:** 2\
**Page:** 1

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**Author:** ![Dr\_Gopal\_Dabade](https://avatars.discourse-cdn.com/v4/letter/d/b487fb/32.png) [@Dr\_Gopal\_Dabade](https://talk.edrugplus.org/u/Dr_Gopal_Dabade)\
**Post date:** [September 20, 2008, 4:08pm UTC](https://talk.edrugplus.org/t/e-drug-pneumonia-vaccine/30549/1 "2008-09-20T16:08:00Z")

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E-DRUG: Pneumonia vaccine  
--------------------------------------------------

[Copied as fair use]

OUTLOOK, India, Sep 08, 2008  
DEBARSHI DASGUPTA  
[http://www.outlookindia.com/fullprint.asp?choice=1&fodname=20080908&fname=Vaccine+(F)&sid=1](http://www.outlookindia.com/fullprint.asp?choice=1&fodname=20080908&fname=Vaccine+%28F%29&sid=1)

India plans to adopt a pneumonia vaccine that doesn't work and has ill side-effects

A pneumonia vaccine the government wants to introduce into the  
immunisation programme is suspect:

&nbsp;&nbsp;\* The vaccine, Prevenar, is not effective against the most common form  
of pneumonia

&nbsp;&nbsp;\* It just prevents 3.6 instances of radiological pneumonia, a rarer form  
of pneumonia, in every 1,000 children vaccinated

&nbsp;&nbsp;\* It causes severe respiratory disease in every 1.3 cases per 1,000  
vaccinated

&nbsp;&nbsp;\* The vaccine, costing Rs 12,000 for three required doses, is supported  
by foreign donor agencies and the WHO

How would you react if you were told that your child had contracted a  
lifelong ailment because of the side-effects of a vaccine that is part of the  
government's immunisation programme? And what if it's discovered that  
the vaccine didn't even offer protection in the first place against the  
disease it was meant to provide immunity from? It all sounds incredible,  
but may well be true if foreign donor agencies and pharmaceutical firms  
have their way with the government.

It has been revealed that the pneumococcal conjugate vaccine (PCV), a  
vaccine against pneumonia that the Union ministry of health and family  
welfare reportedly plans to include in a year's time in its universal  
immunisation programme, causes severe respiratory disorder in every  
one child among a thousand vaccinated. For India, that could potentially  
mean several thousands of victims of asthma and respiratory diseases.

Not only that, the vaccine, which covers seven strains of the  
pneumococcus bacteria, has been found to be ineffective against the  
most common form of pneumonia clinical pneumonia. PCV7, as the  
vaccine is commonly referred to, also happens to be very expensive.  
Launched in the Indian market in 2006 under the brand Prevenar, it is  
available at a cost of about Rs 12,000 for the three required doses. On  
the other hand, the standard treatment of pneumonia using Septran, as  
recommended by the WHO, costs only Rs 10.

Highlighting these facts, Jacob Puliyel and Sona Chowdhary, both  
paediatricians at New Delhi's St Stephen's Hospital, have written to the  
WHO, questioning claims of the vaccine's efficacy. Their letter has just  
been published in the WHO bulletin. The two culled the facts from studies  
analysed by the Cochrane Collaboration, a voluntary global network that  
reviews healthcare interventions. "We found this vaccine does not reduce  
incidence of clinical pneumonia. It just prevents 3.6 cases of radiological  
pneumonia per thousand children vaccinated and that too if they are  
under the age of two, after which the vaccination is ineffective," says  
Puliyel. Even this marginal benefit comes at a high price, leave aside the  
additional cost of treating 1.3 cases of asthma per thousand caused by  
the vaccine.

In response, the WHO bulletin has also published a reply from a panel of  
three experts who admit the vaccine does not reduce instances of clinical  
pneumonia, but, paradoxically, cite the 155.8 million worldwide cases of  
clinical pneumonia as good reason to introduce the PCV. They, however,  
argue that the vaccine is effective in preventing radiological pneumonia  
and that the respiratory side-effect should be weighed against this  
benefit. Clinical pneumonia is the kind that can be diagnosed with the  
help of symptoms such as breathlessness and cough. Radiological  
pneumonia, on the other hand, can only be detected through an x-ray that  
shows the infected patch in the lungs. The former form of the disease is  
far more common than the latter.

Prevenar, manufactured by US-based Wyeth, has been propped up  
internationally by GAVI Alliance, a group that funds immunisation  
initiatives.It has been supported by the WHO. The two have been urging  
developing countries to adopt and integrate the PCV7 into their  
immunisation programmes. India seems to be getting there. Health  
secretary Naresh Dayal, in an interview to The Times of India in April this  
year, had declared the vaccine would be introduced in the immunisation  
programme in a year's time. Dayal did not reply to the questions Outlook  
sent him by fax. GAVI, on the other hand, in an e-mailed reply, confirmed  
the government's intent to introduce the pneumococcal vaccine. "Earlier  
this year, the Indian National Technical Advisory Group for Immunisation  
subcommittee recommended introduction of pneumococcal vaccine  
beginning in one state in 2010 and reaching universal coverage by 2015,"  
wrote Ranjana Kumar, who's on GAVI's country support team.

M.K. Bhan, secretary, department of biotechnology and head of the  
immunisation subcommittee, says he is surprised: "I don't know where  
GAVI got that information from. We recommended the use of a vaccine  
against pneumonia whenever an affordable, locally manufactured, safe  
and efficacious vaccine is available. It should also cover at least 70 per  
cent of the strains in India."

This brings up a prickly and emotive issue in India's public health  
discourse, where many feel that vaccines are thrust upon countries by  
donor agencies and pharmaceutical firms with no concern for the local  
disease burden and other factors such as varying natural immunity. The  
extensive immunisation programme, they feel, is under constant pressure  
as it assures a captive market. "Local factors are important for a vaccine's  
introduction," says Y. Madhavi, a vaccine policy analyst at Delhi-based  
National Institute of Science, Technology and Development Studies.  
"There is growing evidence that a vaccine that is suitable elsewhere may  
not be effective here. For instance, children with poor immunity may fail to  
react positively to a vaccine," she adds.

WHO estimates that each year pneumonia kills about 4,08,000 children  
under the age of five in India but authentic data from local  
population-based studies is missing. "In the absence of any such data, a  
vaccine's introduction is questionable," says C.M. Gulhati, editor of  
Monthly Index of Medical Specialties. "And in any case, this vaccine  
doesn't merit consideration because it doesn't cure all kinds of pneumonia  
and its benefits (3.6/1000) are marginal compared to the severe  
side-effects it has (1.3/1000)."

The campaign by GAVI and WHO to introduce the PCV7 in India's  
immunisation programme has been going on for a while. In 2007, writing  
in the journal Indian Pediatrics, Thomas Cherian of the WHO's  
department of immunisation and Orine S. Levine of GAVI's PneumoADIP  
wrote that the Indian government, if it chooses, could obtain the vaccine  
with financial aid from GAVI till 2015. The latter also wrote to the  
government in April 2007 asking for "non-binding expressions of interest"  
in introducing pneumococcal vaccines. To which, Puliyel responds  
sarcastically, "Is this an introductory offer for a product that they want  
to sell?" GAVI's Kumar confirmed that the Indian government has to specify  
while applying for support on how it plans to secure funds for sustaining  
the vaccine costs beyond the period of GAVI's funding.

Observers hope that a debate on the issue brings about a more stringent  
and reliable mechanism of deciding on vaccines being introduced in the  
country. While it's imperative that children need to be protected against  
pneumonia, the choice of the vaccine is critical. If it does not even  
provide immunity, then why should public money be wasted on it?

Gopal Dabade,  
57, Tejaswinagar,  
Dharwad 580 002  
Tel 0836-2461722  
Cell (0)9448862270  
www.jagruti.org  
www.aidanindia.org  
www.daf-k.cjb.net

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**Author:** ![Donald\_Light](https://avatars.discourse-cdn.com/v4/letter/d/ecccb3/32.png) [@Donald\_Light](https://talk.edrugplus.org/u/Donald_Light)\
**Post date:** [September 21, 2008, 3:55pm UTC](https://talk.edrugplus.org/t/e-drug-pneumonia-vaccine/30549/2 "2008-09-21T15:55:26Z")

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E-DRUG: Pneumonia vaccine (2)  
----------------------------------------------------

I know quite a lot about this. GAVI behaves as if it is an agent for Wyeth  
and other major companies for making additional profits from sales to  
low-income countries by paying prices several times costs and covering the  
difference with donors' contributions. This keeps countries dependent on  
charity and protects the companies' IP rights and pricing strategies.

In this case, it is my impression as a non-expert that offering the 7-valent  
vaccine at a subsidized price can be dangerous, since it will protect  
against some serotypes in developing countries and therefore allow the  
others to proliferate. When I asked a GAVI officer about this concern of  
vaccine experts, he said GAVI thought by the time that problem arose, GAVI  
would have the 10- or 13-valent new vaccines to administer. It does not  
sound like a good idea to me as a policy researcher for political and  
cultural reasons -- administering a vaccine that does not work well could  
create a bad taste and backlash. But clearly it will allow Wyeth to make a  
few dollars a dose profit on large volume on this vaccine, before they phase  
it out and replace it with their 13-valent one.

You probably know my published concerns about AMCs being designed as  
vehicles for new profits for major companies that minimize children saved  
per billion donated. They have appeared in The Lancet and PLoS Medicine, and  
some are found at [http://bioethics.upenn.edu/people/?last=Light&first=Donald](http://bioethics.upenn.edu/people/?last=Light&first=Donald)

Donald Light  
Visiting researcher, Center for Migration and Development  
Professor, UMDNJ  
Leverhulme Trust Visiting Professor (UK) 2008  
Tel: 1-609-216-0071  
E-mail: dlight@Princeton.edu
