Analgesics - Opioids
Pharmacy Help Desk - (800) 522-0114 option 4
Opioid Prescribing guidelines can be found at www.okhca.org/opg
Prescribing guidelines and quantity limits for Analgesic, NSAIDs, and Antipyretics
| Date of Quantity Limit Implementation | Medications Affected |
|---|---|
Phase 1 - November 2014 |
|
Phase 2 - December 2014 |
|
Phase 3 -January 2015 |
|
Short Acting Opioid Analgesics - Alphabetically by Generic Name (Oral and Topical ONLY)
Drug Generic Name | Drug Brand Name | Quantity Limit Amount per 30 Days |
Acetaminophen/Codeine | Tylenol with Codeine # 2®, Tylenol with Codeine #3®, Tylenol with Codeine #4® | 120
|
Codeine Acetaminophen, Aspirin, Butalbital Combination Products | Cogesic®, Fioricet®, Fiorinal with Codeine® Ascomp® | 180 |
Dihydrocodeine acetaminophen, aspirin, caffeine combination products | Synalgos®, Trezix® | 120 |
Codeine Sulfate | Codeine | 120 |
Fentanyl oncology formulations | Actiq®, Subsys® Fentora® Abstral® | 120 112 128 |
Hydrocodone – Acetaminophen | Norco®, Vicodin®, Lorcet®, Maxidone®, Xodol®, Zamicet®, Primlev® | 120 |
Hydrocodone-Ibuprofen | Vicoprofen®, Reprexian®, Ibudone® | 120 |
Hydromorphone HCL | Dilaudid® | 120 |
Meperidine | Demerol®, Meperitab® | 64 per 8 days |
Morphine Sulfate Immediate Release | MSIR® | 120 |
Oxycodone - Acetaminophen | Percocet®, Magnacet®, Roxicet® | 120 |
Oxycodone - Aspirin | Percodan®, Endodan® | 120 |
Oxycodone - Ibuprofen | Combunox®, Xylon-10® | 120 |
Oxycodone - Acetaminophen | Percocet®, Magnacet® | 120 |
Oxycodone Immediate Release | OxyIR®, Roxicodone®, Oxecta® | 120 |
Oxymorphone Immediate Release | Opana IR® | 120 |
Tapentadol | Nucynta® | 120 |
Tramadol | Ultram® | 240 |
Tramadol- Acetaminophen | Ultracet® | 180 |
Long Acting Opioid Analgesics - Alphabetically by Generic Name (Oral and Topical ONLY)
Drug Generic Name | Drug Brand Name | Quantity Limit Amount per 30 Days |
Buprenorphine transdermal | Butrans® | 10 |
Fentanyl transdermal system | Duragesic® | 10 |
Hydrocodone Extended Release | Zohydro ER®, Xartemis XR® | 60* and 120** |
Hydromorphone Extended Release | Exalgo® | 30* |
Levorphanol | Levo-dromoran® | 60 |
Morphine Controlled Release | MS Contin® | 90 |
Morphine Extended Release Capsule | Avinza® | 30 |
Morphine Extended Release Capsule | Kadian® | 60 |
Morphine Sulfate- Naltrexone | Embeda® | 60 |
Oxycodone Controlled Release | Oxycontin® | 60 |
Oxymorphone Extended Release | Opana ER® | 60 |
Tapentadol | Nucynta ER® | 60 |
Tramadol Extended Release | Ultram ER®, Ryzolt®, ConZip® | 30 |
* Special PA or other restrictions apply
** Xartemis XR special PA or other restrictions apply
Clinical Notes:
Acetaminophen Hepatotoxicity
- Acetaminophen has been associated with severe hepatotoxicity following acute and chronic ingestion.
- Maximum recommended dose of acetaminophen for adults is (4) four grams/day.
- Be sure to consider and ask about all potential sources of acetaminophen (e.g., OTC, combination analgesics) when determining daily acetaminophen dose.
- Risk may increase with concurrent alcohol use, underlying liver disease, and/or the fasting state.
Constipation
- Common adverse effect with chronic opioid use; prescribe stool softener +/- laxative with narcotic.
Black Box Warning – Long-acting opioid analgesics
The FDA requests that practitioners who prescribe extended-release and long-acting opioid analgesics should be used ONLY for pain severe enough to require daily, around-the-clock long-term opioid treatment for which alternative therapies are inadequate. Due to the risk of addiction, abuse, and misuse, these drugs should be reserved for patients in whom non-opioid alternatives or immediate-release opioids have not been tolerated or ineffective in managing pain.
The FDA has approved class-wide label changes for ALL extended release and long acting opioid products. In addition, a the black box warning cautions that long-term maternal use of opioid analgesics during pregnancy can lead to neonatal opioid withdrawal syndrome, which can be life-threatening.
Please reserve these medications for only the most severe pain and consider tapering and withdrawing these products whenever possible.
For more information visit the FDA website here: http://www.fda.gov/Drugs/DrugSafety/InformationbyDrugClass/ucm363722.htm
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