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    “While we’ve come to agree that the drug schedule should be based on science and not politics, this bill is still a bad bill,” AMA’s President R. Gil Kerlikowske said in a statement. “There are no conditions that an MAO-B or other medical drug would require under this bill, making it very difficult to determine whether these drugs are safe or effective, not to mention the potential for abuse.”

    Many of the drug companies will not be happy about the bill either. After the Food and Drug Administration announced last week that it would not reschedule a drug to treat depression from Schedule 3 to Schedule 1, Eli Lilly announced in a statement that the “Congressional version of the S. 744 would significantly shift from the current regulatory regime to one based on unproven and speculative notions.” The FDA would have to wait four years for the new schedule to take effect, which may not happen until the middle of 2016.

    “We are deeply concerned the proposal to further increase the length of time a drug can remain controlled under the law would allow pharmaceutical company marketing exclusivity to expire,” said Eli Lilly.

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    In the past, drug makers have pushed to expand the number of drug scheduling exceptions to include antidepressants, drugs that help people with mental illnesses, anti-epileptic drugs, and even drugs that are only approved by the FDA for certain conditions. The new restrictions are likely to add additional restrictions to this list in the future.

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