Editor, – The comment
in comment in Australian
Prescriber (2007;30:91)
(2007;30:91) draws unhelpful and
misleading parallels between complementary medicines
today and 'dangerous and useless medicines'
available 100 years ago.
The author is right to point to the establishment of
the Therapeutic Goods Administration (TGA) as an
important landmark for the regulation of
pharmaceuticals and complementary medicines. The
Complementary Healthcare Council (CHC) fully
supports a regulatory process that safeguards
consumer interests. However, to suggest that
complementary medicines as therapeutic goods are
somehow compromised by false or misleading
advertising or that barriers exist to understanding
them because sponsors hide behind
'commercial-in-confidence' is inaccurate.
All advertisements for therapeutic goods are subject
to the Therapeutic Goods, Trade Practices and other
relevant laws. The Therapeutic Goods Advertising
Code, which applies to advertisements directed to
consumers and where sanctions apply for breaches,
requires material to be truthful, balanced, not
contain misleading or exaggerated claims, and all
descriptions, claims and comparisons must be able to
be substantiated.
With regard to 'commercial-in-confidence', it is hard
to see how concerns regarding transparency would not
equally apply to pharmaceutical companies. Companies
responsible for marketing products are obliged to
make available all evidence regarding claims in
relation to their products, should they be asked to
do so by the TGA.
What does concern the CHC, is the outdated attitudes
demonstrated towards complementary medicines,
despite repeated and compelling evidence
demonstrating their health benefits. Let's imagine
for one moment the implication for pregnant women
globally, if folate supplementation in preventing
neural tube defects had not become accepted
mainstream practice.
Tony Lewis
Executive Director
Complementary
Healthcare Council
Canberra