1. The Diversion of Ultram®, Ultracet®, and Generic Tramadol HCl
- Author
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James A. Inciardi, Anne Geller, Edgar H. Adams, Edward C. Senay, Alvaro Muñoz, George E. Woody, and Theodore J. Cicero
- Subjects
Narcotics ,Risk ,Tramadol hcl ,Steering committee ,Advisory Committees ,Medicine (miscellaneous) ,Postmarketing surveillance ,Drug Prescriptions ,Food and drug administration ,Generic drug ,Product Surveillance, Postmarketing ,Drugs, Generic ,Humans ,Medicine ,Drug Approval ,Tramadol ,Acetaminophen ,Marketing ,Controlled substance ,Illicit Drugs ,United States Food and Drug Administration ,business.industry ,Data Collection ,General Medicine ,Opioid-Related Disorders ,medicine.disease ,United States ,Drug Combinations ,Psychiatry and Mental health ,Clinical Psychology ,Cross-Sectional Studies ,Drug and Narcotic Control ,Medical emergency ,business ,human activities ,medicine.drug - Abstract
Ultram (tramadol HCL) was approved by the Food and Drug Administration in 1994 as a non-scheduled drug under the Controlled Substance Act. The non-scheduled status was contingent on the development and implementation of a comprehensive post-marketing surveillance program by an Independent Steering Committee external to Ortho-McNeil Pharmaceutical charged with monitoring abuse and recommending scheduling if unexpectedly high abuse occurred. The program developed by this committee was composed of a variety of studies, and the results of the first three years of the surveillance efforts revealed that the rate of Ultram abuse was low. At a meeting of the FDA in 1998 to reexamine the scheduling status of Ultram, it was recommended that the scope of the postmarketing surveillance program be broadened to include data on diversion. After a 1-year pilot study, by January 2002, a nationwide diversion survey was fully operational. This brief communication describes the experiences of this diversion study, and compares the findings on the diversion of Ultram and other tramadol HCL products with that of more widely abused drugs. Survey data suggest that the diversion of Ultram and other tramadol products is low, and overall, diversion investigators did not consider tramadol to be a problem in their respective jurisdictions.
- Published
- 2006