The U.S. Food and Drug Administration approved a single shared Risk Evaluation and Mitigation Strategy (REMS) for the transmucosal immediate-release fentanyl (TIRF) products. This new shared system will replace the individual REMS and allow prescribers and pharmacies to enroll into just one system, easing the burden on the health care system.
TIRF medicines, which include the brand-name drugs Abstral, Actiq, Fentora, Lazanda, and Onsolis, are narcotic pain
medicines called opioids used to manage pain in adults with cancer
who routinely take other opioid pain medicines around-the-clock.
The shared system strategy, called the TIRF REMS Access Program, will be used by all sponsors of TIRF products and is expected to ease the burden on the health care system. The program will begin in March, 2012. Until that time, prescribers, patients, and pharmacies should continue to enroll in the individual REMS programs.
"This TIRF REMS will ensure safe use and access to these drugs for patients who need them," said Janet Woodcock, M.D., director of the FDA's Center for Drug Evaluation and Research. "We have worked with the sponsors of both the innovator and generic drugs to develop this single, shared system that will streamline the process and decrease the burden of the REMS on the health care system."
The goals of the TIRF REMS Access Program are to ensure patient access to important medications and mitigate the risk of misuse, abuse, addiction, overdose and serious complications due to medication errors by:
-- prescribing and dispensing TIRF medicines only to appropriate patients, including use only in opioid-tolerant patients.
-- preventing inappropriate conversion between fentanyl products.
-- preventing accidental exposure to children and others for whom TIRF medicines were not prescribed
-- educating prescribers, pharmacists, and patients on the potential for misuse, abuse, addiction, and...