FDA Panel Wants Tighter Controls over Pain Pills
January 29, 2013
A US Food and Drug Administration advisory panel voted last Friday to recommend that popular pain relievers containing the opioid hydrocodone be moved from Schedule III to Schedule II of the Controlled Substances Act. Popular prescription drugs containing hydrocodone include Vicodin and Lortab.
That would put Lortab and Vicodin in the same schedule as morphine and Oyxcontin, which contains oxycodone.
If the FDA agrees with its advisory panel and reschedules hydrocodone, pain patients using the drug will have to go the doctor’s office to get prescriptions written twice as frequently as now. Schedule III drugs can be prescribed for up to six months at a time, while Schedule II drugs can only be prescribed for three months without another visit to the doctor.
The FDA has for years resisted efforts to tighten controls over hydrocodone, saying it could limit patients’ access to pain medicine, but as overdose deaths and addiction rates from prescription pain relievers have jumped in recent years, pressure has been mounting on the agency. The agency is acting now after receiving a request from the DEA to consider rescheduling.
The advisory panel’s 19-10 vote received mixed reviews from experts consulted by the Milwaukee Journal-Sentinel.