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Parenteral Manual |
Nalbuphine
Disclaimer: Official controlled document is the CHEO online copy. It is the responsibility of user to ensure that any paper copy version is the same as the online version before use.
Classification:
Analgesic, Narcotic; Opiate Partial Agonist
Indications:
- Prevention or treatment of opiod-induced pruritis
Reconstitution and Stability:
- Nalbuphine is available as 10 mg/mL solution for injection in 1 mL ampoules
- Store at room temperature; protect from excessive light; store in carton until used
Compatibility:
- Solution Compatible: Dextrose up to D10, 0.9% NaCl, Ringer's Lactate
- Additives/Above Cassette Compatible: None
- Y-site Compatible: Cefazolin, Cefotaxime, clindamycin, diphenhydramine, midazolam, metronidazole, ranitidine, KCl
Incompatible: diazepam, dimenhydrinate, furosemide, hydrocortisone, ketorolac, methylprednisolone, piperacillin, piperaciilin/tazobactam
Administration:
(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)
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SC
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YES |
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IM
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YES |
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IV Direct
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YES - Undiluted
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IV Intermittent Infusion
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Yes
Usual dilution: 0.1 mg/mL
Infusion time: 5-10 minutes; larger dose should be administered over 10-15 minutes
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IV Continuous Infusion
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NO |
Dosage:
(For neonatal dosages, refer to Neonatal IV Drug Manual.)
Pediatric:
- Opioid induced pruritus: 0.05 mg/kg/dose (Max 5 mg/dose) IV Q4-6H PRN
Adult:
- Opiod induced pruritus: 2.5 - 5 mg IV; may repeat dose
Potential hazards of parenteral administration:
- hypotension, tachycardia, bradycardia
- drowsiness, dizziness, dysphoria, sedation
- urticaria, pruritus, hypersensitivity reactions
- nausea, vomiting
- urinary retention
- respiratory depression
- blurred vision
Notes:
- Monitor: respiratory and mental status, blood pressure, pulse
- Analgesic potency: 1 mg = 1 mg morphine
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