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New Safety Measures Announced for Immediate Release (IR) Opioids

New Safety Measures Announced for Immediate Release (IR) Opioids

[9/18/2018] FDA approved the Opioid Analgesic REMS, which applies to all opioid analgesics intended for outpatient use. The REMS program requires that training be made available to all health care providers who are involved in the management of patients with pain, including nurses and pharmacists. The agency also approved the FDA Education Blueprint for Health …

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New Safety Measures Announced for Extended-release and Long-acting Opioids | FDA

New Safety Measures Announced for Extended-release and Long-acting Opioids | FDA

[9/18/2018] FDA approved the Opioid Analgesic REMS, which applies to all opioid analgesics intended for outpatient use. The REMS program requires that training be made available to all health care providers who are involved in the management of patients with pain, including nurses and pharmacists. The agency also approved the FDA Education Blueprint for Health …

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New Safety Measures Announced for Opioid Analgesics, Prescription Opioid Cough Products, and Benzodiazepines | FDA

New Safety Measures Announced for Opioid Analgesics, Prescription Opioid Cough Products, and Benzodiazepines | FDA

[8-31-16] After an extensive review of the latest scientific evidence, the U.S. Food and Drug Administration announced today that it is requiring class-wide changes to drug labeling, including patient information, to help inform health care providers and patients of the serious risks associated with the combined use of certain opioid medications and a class of …

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Oxymorphone (marketed as Opana ER) Information

Oxymorphone (marketed as Opana ER) Information

Opana ER (oxymorphone hydrochloride extended-release tablets) was first approved in 2006 for the management of moderate-to-severe pain when a continuous, around-the-clock opioid analgesic is needed for an extended period of time. The product, currently marketed by Endo Pharmaceuticals, is a reformulation of the original product, designed with physicochemical properties intended to make the drug resistant …

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Opioid Timeline

Opioid Timeline

1995.  OxyContin (oxycodone controlled-release) approved; first formulation of oxycodone that allowed dosing every 12 hours instead of every 4 to 6 hours.   1998.  Actiq (fentanyl) approved; first pain medicine approved to treat cancer breakthrough pain, but with additional safety measures.   Early 2000s.  Reports of overdose and death from prescription pain drugs, especially OxyContin, …

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Safe Opioid Disposal – Remove the Risk Outreach Toolkit

Safe Opioid Disposal – Remove the Risk Outreach Toolkit

En Español Remove the Risk raises awareness of the serious dangers of keeping unused opioid pain medicines in the home and provides information about safe disposal of these medicines. Use these free toolkit materials—public service announcements (PSAs), social media images and posts, fact sheets, and more—for talking with others about safe opioid disposal. Remove the …

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FDA takes action against 53 websites marketing unapproved opioids as part of a comprehensive effort to target illegal online sales

FDA takes action against 53 websites marketing unapproved opioids as part of a comprehensive effort to target illegal online sales

For Immediate Release: June 05, 2018 Español The U.S. Food and Drug Administration today announced that it has warned nine online networks, operating a total of 53 websites, that they must stop illegally marketing potentially dangerous, unapproved and misbranded versions of opioid medications, including tramadol and oxycodone. Companies who fail to correct the violations, as …

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Opioid Analgesic Drugs: Considerations for Benefit-Risk Assessment Fra

Opioid Analgesic Drugs: Considerations for Benefit-Risk Assessment Fra

Docket Number: FDA-2019-D-1536 Issued by: Guidance Issuing Office Center for Drug Evaluation and Research The purpose of this guidance is to describe the benefit-risk assessment framework that the 17 Agency uses in evaluating whether applications for opioid analgesic drugs meet the standard for 18 approval under section 505 of the Federal Food, Drug, and Cosmetic …

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Website Disclaimer

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