FDA opioid black box

March 24, 2016

ATTEMPTING to educate prescribers and patients about the risks related to opioid use, the U.S. Food and Drug Administration has announced required classwide safety labelling changes for immediate-release opioid pain medications. The FDA now requires a new boxed warning about the serious risks of misuse, abuse, addiction, overdose and death, while other labelling changes include additional information on the serious risks associated with this class of drug. One of the other warnings relates to use during pregnancy and the enhanced risk of neonatal opioid withdrawal syndrome (NOWS).

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Pharmacy Daily | FDA opioid black box

FDA opioid black box

Other recent headlines

PD breaking news – Queensland pharmacies scope of practice pilot expanded

Commbank to help navigate ownership

Littleproud visits Orana Mall

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES