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MHCP Enrolled Providers – Pharmacies Fee-for-Service PA Criteria Sheet – Butrans (March 2011) Drug Strengths Butrans (buprenorphine) transdermal patches [Purdue] 5 mcg/hour, 10 mcg/ hour, 20 mcg/hour FDA approved indication Butrans (buprenorphine) is indicated for the management of moderate to severe chronic pain in patients requiring a continuous, around-the-clock opioid analgesic for an extended period of time. Butrans is a transdermal system (patch) providing systemic delivery of buprenorphine continuously for 7 days. Criteria Patient has chronic pain requiring opiate therapy The patient has been tried on sustained release morphine but experienced intolerable adverse events. Ineffectiveness of morphine to control pain is not a criteria for approval Quantity Limits Apply: Only 4 patches per fill and only one strength allowed per patient. The maximum dose of Butrans per label is 20 mcg/hour per label. Butrans 15 mcg/ hour (one 5 mcg/hour [patch and one 10 mcg/hour patch) will not be approved. Exclusion Criteria Payment for Butrans will be denied in the following situations: Butrans is add-on therapy to another long acting opioid. If patient is being transitioned from one opioid to Butrans, then a discontinuation plan of the first opiod must be provided Patient’s current long acting ± short acting opioid dose is >80 mg morphine equivalents per day Patient’s current opiate is fentanyl patch strengths ≥50 mcg/hour Approximate opioid equivalents to oral morphine Total mg per day Morphine 80 mg/day Codeine 250 mg/day Hydrocodone 40 mg/day Hydromorphone 10 mg/day Meperidine 400 mg/day Methadone 30 mg/day Oxycodone (OxyContin) 40 mg/day Pentazocine 240 mg/day Tramadol 800 mg/day MHCP Provider Call Center (651) 431-2700 or 1-800-366-5411