Two years ago, on June 23, 2005, the U.S. Food and Drug Administration approved the first “ethnic” drug. Called BiDil (pronounced “bye-dill”), it was intended to treat congestive heart failure—the progressive weakening of the heart muscle to the point where it can no longer pump blood efficiently—in African-Americans only. The approval was widely declared to be a significant step toward a new era of personalized medicine, an era in which pharmaceuticals would be specifically designed to work with an individual’s particular genetic makeup. Known as pharmacogenomics, this approach to drug development promises to reduce the cost and increase the safety and efficacy of new therapies. BiDil was also hailed as a means to improve the health of African-Americans, a community woefully underserved by the U.S. medical establishment. Organizations such as the Association of Black Cardiologists and the Congressional Black Caucus strongly supported the drug’s approval.
A close inspection of BiDil’s history, however, shows that the drug is ethnic in name only...
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This is always a dicey territory when they start to develop drugs catered to ethnicities. Granted there are genetically-linked diseases and illnesses, (i.e. Tay-Sachs, Sickle Cell, etc.)
ReplyDeleteI guess we'll see where it goes.
You know what would solve this problem is a giant-sized orgy! Everyone should just start screwing--every ethnic groups, every religion, every culture-- eliminating disease and the need for lame pharmaceuticals.
Of course, that suggestion would come out of the head of standup comedienne!