It is estimated that 42% Of the American public is using some form of alter
native medicine, which reflects the changing needs and values in our societ
y. Unfortunately, Western medicine has failed to see alternative medicine a
s complementary and integrative with conventional medicine. This is due to
the fact that there is very little scientific data available regarding the
safety, efficacy, optimal dosage and side-effects or interactions of these
alternative medicine therapies. Many physicians dismiss a patient's questio
ns concerning alternative medicine because the physician believes it is "qu
ackery," without any proof to support this claim. This violates the patient
's right to full disclosure of all possible treatment options and encourage
s patients to use these therapies without their physician's knowledge. As a
result, it is estimated that 46% of those using alternative medicine do so
without the supervision of their primary care physicians or alternative me
dicine practitioners. At the present time there is no regulatory process to
ensure the safety and efficacy of these alternative medicine therapies. Ma
nufacturers do not have to prove that their product works, but they must en
sure that their product is not harmful. The combination of failure to infor
m physicians of usage and the possibility of adverse reactions with prescri
ption drugs is placing the lives of many Americans in jeopardy. Ethically,
consumers have the right to use alternative medicine therapies as a matter
of autonomy, but they also have the duty not to harm themselves. To ensure
their safety, alternative medicine therapies must be evaluated in regards t
o safety and efficacy so that they can be integrated into conventional medi
cine. The Federal Drug Administration has the ethical responsibility to tak
e the lead in this area. To protect the common good, there is a need to kno
w not only what alternative medicine can do for us but what it can do to us
.