Article review - “Manslaughter by Fake
Artesunate in Asia – Will Africa be Next?”
by Paul N. Newton*, Rose McGready, Facundo
Fernandez, et al; (published in PloS Medicine, June 2006, Volume 3, Issue e197)
The authors warn of counterfeit (fake)
“artesunate” tablets (containing no artesunate) in Asia. Examples of fake
artesunate samples collected in various parts of Africa including Cameroon and
Tanzania are also provided. According to the article, fake drug
(dihydroartemisinin 60 mg per tablet, Cotexcin) was found in Tanzania in 2001,
labeled as made by Beijing COTEC New Technology Corp and was found to have no
dihydroartemisinin or other active drug when analysed. The packaging of the
counterfeit Cotexcin found in Tanzania was smaller than the genuine pack. More
striking, while the genuine Cotexcin pack had a diagram of mosquito, the fake
one didn’t have. According to the authors, fake artesunate do not always lack
active drug, e.g. in 2005 in Burma, fake artesunate labeled as made by Guillin
Pharmaceutical (Guangxi, Peoples Republic of China) was found to have
paracetamol as the main drug and artesunate content was 10mg per tablet instead
of 50 mg (as in the genuine product). And in 2005 fake artenunate tablets
mimicking Arsumax (50mg per tablet, Sanofi Synthelabo, Bridgewater, New Jersey,
United States) were found in Cameroon, labeled as Arsuman, manufactured by
Sanofi Synthelabo, and on analysis was found to have the correct amount of
artesunate, 50mg per tablet.
The authors explain why people do make fake
artesunate. The artemisin derivatives are known to be remarkably effective in
their antimalarial effect and are well tolerated. Therefore the demand for
these medicines is high. But since they are expensive, the relatively cheaper
versions would be attractive amongst the poor and the most vulnerable – hence
the conterfeiters target this group.
The dangers of fake artesunate are many. There
are documented cases of deaths from malaria in endemic areas due to treatment
with fake artesunate. The travelers and tourists from non-malarious areas, may
buy such drugs for self-medication are also at high risk. Other dangers of fake
artesunate with lower drug content include the risk of selection and spread of
artermisinin resistant parasites, which will lead to loss of effective
antimalarial drug and subsequent failure of malaria control initiatives.
Unfortunately, the simple screening tests used
in various parts of Africa for quality of drugs such as colour reaction tests
may not easily detect all fake drugs. Therefore, the results of such tests may
provide the users of fake artesunate with false sense of confidence.
The authors propose some ways for preventing
the rapid spread of fake artesunate in Africa. Control of medicines importation
is a good attempt but difficult to maintain due to porous borders. Provision of
subsidized genuine artesunate containing drugs through the public facilities
shall ensure the drugs are sourced from reputable sources and are made
available at reduced prices and there would be no financial advantage of buying
from other sources. While this option is attractive, there are many cases of
malaria that are treated via private clinics / hospitals. Such private clinics
/ hospitals including Church facilities should be included in the Government
subsidy programme, so that they do not become a potential target for fake
artemisinin containing drugs.
*The article was summarized with permission
from Paul N. Newton.