A new piece of legislation introduced in the Senate last week would see the involvement of the US Food and Drug Administration (FDA) in a panel of experts meant to curb the rising tide of prescription drug abuse.
The legislation, the Combating Prescription Drug Abuse Act (CPDA), was introduced on 10 July 2013 by Sen. Barbara Boxer (D-CA) and would establish a commission of experts and stakeholders known as the Combating Prescription Drug Abuse Commission.
That commission would be composed of a wide range of agency officials and other public stakeholders, including representatives from:
Both FDA and DEA would have prominent positions on the committee, serving as co-chairs. The committee itself will be charged with reviewing current efforts to prevent and reduce the abuse of prescription drugs, making a report to Congress on those efforts, identifying opportunities to better prevent or reduce drug abuse and recommending ways to reduce diversion of abused prescription drugs.
The report to Congress would involve a minimum of ten recommendations on the following topics, according to the legislation:
The committee would not be a long-term fixture, with its term expiring two years after the appointment of its members (required within 180 days) and its funding limited to $3 million over the 2014-2016 period.