Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
BMJ 2004;328:603 (13 March), doi:10.1136/bmj.328.7440.603
Washington Charles Marwick
Heavy lobbying by the US drug industry has, for the time being, held up studies comparing the clinical efficacy of prescription drugs. The Centers for Medicare and Medicaid Services (CMS), which administers Medicare, has been effectively prevented from using evidence of functional equivalence when deciding whether or not Medicare should approve a particular drug for coverage and Medicaid programmes.
The drug companies argued, prior to legislation being passed, that attempts to determine equivalence between older and most likely cheaper drugs, would discourage manufacturers from developing new and possibly better products, even though they were likely to be more expensive.
Last year Congress considered legislation requiring such comparisons (BMJ 2003;327:642). By the time the President signed into law the new Medicare legislation in December, however, the funding for comparative studies had been eliminated from the President’s proposed 2004-5 budget.
The law also said that the CMS did
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
StumbleUpon
Technorati What's this?
Read all Rapid Responses