SAFE Opioid Prescribing: ER/LA Opioids – Perspectives on Patient Assessment and Therapy Management
Today, clinicians are faced with the challenge of adequately treating a large number of patients with acute and chronic pain, while mitigating the risks associated with treatment. Our ability to manage pain, now competes against the crisis of opioid abuse and adverse outcomes such as addiction, unintentional overdose, and death, resulting from inappropriate prescribing, abuse, and misuse of opioids.
These complexities require clinicians to have a strong understanding of all options for pain management including non-pharmacologic and non-opioid options, as well as when to appropriately consider opioid agents when other non-opioid approaches have proven unsuccessful in alleviating pain and the benefits outweigh the risks.
The SAFE Opioid Risk Evaluation and Mitigation Strategy (REMS) symposium is designed to fulfill on specific requirements put forth by the FDA Education Blueprint for HCPs Involved in the Treatment and Monitoring of Patients with Pain. Six evidence-based CME modules will address topics such as; the fundamentals of pain management, assessment of patients in pain, identifying and mitigating risk factors for abuse and addiction, and how to appropriately integrate opioid analgesics into a pain treatment plan individualized to the needs of the patient.
Additional topics to be covered include, tools to manage patients on opioids analgesics in pain settings, including initiating therapy, titrating and discontinuing use, as well as strategies to counsel patients on safe use, disposal, and ways to identify and manage opioid use disorder or addiction.
Complete the entire SAFE Opioid Prescribing activity to receive your training completion certificate!
Speaker’s Bureau for Allergan, Inc., Amgen Inc., BioDelivery Sciences International, Inc., Daiichi Sankyo, Inc., and Depomed, Inc. Advisory Board member for Braeburn Pharmaceuticals, Inc., Depomed, Inc., Kaléo Pharma, Pfizer Inc., Quest Pharmaceuticals, Inc., and Teva Pharmaceuticals. Consultant for Nevro and Vertex Pharmaceuticals Incorporated. Contracted Research for Grünenthal GmbH and Vertex Pharmaceuticals Incorporated. Ownership Interest in Depomed, Inc. and Pfizer Inc,
Speakers Bureau member for Collegium Pharmaceutical, Inc. Depomed, Inc., Daiichi Sankyo, Inc., Purdue Pharma L.P, and Teva Pharmaceuticals. Advisory Board member for AstraZeneca Pharmaceuticals LP, Collegium Pharmaceutical, Inc. Depomed, Inc., Daiichi Sankyo, Inc., and Purdue Pharma L.P. Ownership Interest in Cara Therapeutics.
Speakers Bureau member for AstraZeneca Pharmaceuticals LP, Collegium Pharmaceutical, Inc., Daiichi Sankyo, Inc., Purdue Pharma L.P., and Salix Pharmaceuticals Inc. Advisory Board member for Depomed, Inc. Consultant BioDelivery Sciences International, Inc., Nektar Therapeutics, Pernix Therapeutics, and Quest Diagnostics.
Speakers Bureau member for Collegium Pharmaceutical Inc. Advisory Board member for Collegium Pharmaceutical, Inc., Daiichi Sankyo, Inc., Pernix Therapeutics, and Pfizer Inc. Has ownership interests in BioSpecifics Technologies Corp., Collegium Pharmaceutical, Galena Biopharma and Johnson & Johnson.
Non-faculty contributors and others involved in the planning, development, and editing/review of the content have no relevant financial relationships to disclose.
pmiCME is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
pmiCME designates this enduring material for a maximum of 1.50 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
pmiCME is accredited by the American Association of Nurse Practitioners as an approved provider of nurse practitioner continuing education. Provider Number 040308.
This program has been approved for 1.50 contact hours of continuing education, which includes 0.49 hour of pharmacology.
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REMS Program Companies
Miller Medical Communications, LLC
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Clinical judgment must guide each clinician in weighing the possible risks, benefits, or contraindications of any diagnostics, interventions or treatments discussed. Clinicians should review manufacturers’ product information and consider these with the recommendations of other authorities when applying the assessment and/or clinical management strategies discussed in this activity to the care of their patients.
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Discussion of Off-Label Uses and Investigational Products
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