The US Food and Drug Administration (FDA) has underlined that it is serious about ensuring appropriate and rational prescribing of opioids to counteract their misuse, as the agency approved new safety measures governing their use.
In approving the final Opioid Analgesic Risk Evaluation and Mitigation Strategy (REMS), the FDA hopes to help better communicate the risks about the use of these medications to patients and health care professionals.
This expanded REMS now also applies to immediate-release opioid analgesics intended for use in an outpatient setting as well as extended-release and long-acting opioid analgesics, which have been subject to a REMS since 2012.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze