Nalbuphine Dosing Regimen for Pain Management
The standard adult dosing regimen for nalbuphine is 10 mg administered subcutaneously, intramuscularly, or intravenously every 3-6 hours as necessary, with a maximum single dose of 20 mg and a maximum total daily dose of 160 mg. 1
Adult Dosing Guidelines
- Initial dose: 10 mg for a 70 kg individual administered subcutaneously, intramuscularly, or intravenously 1
- Frequency: Every 3-6 hours as necessary 1
- Maximum single dose: 20 mg in non-tolerant individuals 1
- Maximum total daily dose: 160 mg 1
- Dosage should be adjusted according to:
- Severity of pain
- Physical status of the patient
- Other medications the patient may be receiving, particularly CNS depressants 1
Special Clinical Situations
As Supplement to Balanced Anesthesia
- Induction doses: 0.3 mg/kg to 3 mg/kg intravenously administered over 10-15 minutes 1
- Maintenance doses: 0.25 to 0.5 mg/kg in single IV administrations as required 1
For Opioid-Induced Pruritus
- Small doses of 0.5-1 mg IV every 6 hours as needed are effective for treating opioid-induced pruritus without reversing analgesia 2, 3
Titration and Maintenance
- Individually titrate nalbuphine to a dose that provides adequate analgesia while minimizing adverse reactions 1
- Continually reevaluate patients to assess pain control and monitor for adverse reactions 1
- If pain increases after dosage stabilization, identify the source of increased pain before increasing the nalbuphine dosage 1
- If unacceptable opioid-related adverse reactions occur, consider reducing the dosage 1
Pharmacokinetic Considerations
- Mean elimination half-life: 2.2-2.6 hours, regardless of dose or administration route 4
- Time to maximum concentration: 30-40 minutes after intramuscular or subcutaneous administration 4
- Bioavailability: Approximately 80% for both intramuscular and subcutaneous routes 4
- Intramuscular and subcutaneous routes appear to be interchangeable based on pharmacokinetic parameters 4
Recent Research on Optimal Dosing
- For post-operative pain management after laparoscopic surgery, an appropriate administration of nalbuphine is 0.1 to 0.2 mg/kg during the initial four hours, which can be modified to a lower dosage (0.05 mg/kg) later in post-operative management 5
Discontinuation
- When discontinuing nalbuphine in physically dependent patients, taper the dose gradually by 25% to 50% every 2-4 days while monitoring for withdrawal symptoms 1
- If withdrawal symptoms develop, increase the dose to the previous level and taper more slowly 1
- Never abruptly discontinue nalbuphine in physically dependent patients 1
Safety Considerations
- Nalbuphine should be administered only by persons trained in the use of intravenous analgesics and management of respiratory effects of potent opioids 1
- Naloxone, resuscitative equipment, intubation equipment, and oxygen should be readily available 1
- Monitor patients closely for respiratory depression, especially within the first 24-72 hours of initiating therapy and following dosage increases 1
- Nalbuphine has a "ceiling effect" for respiratory depression, but at usual analgesic doses, respiratory depression is comparable to that with morphine 6