Who can administer
Administration RESTRICTED - see Appendix 1
Important information
- To be used by anaesthetists only
- Anaphylactic reactions have been documented, as has cross-reactivity with other neuromuscular-blocking agents
- Dose obese patients based on Ideal Body Weight (Patient is obese if actual body weight is 20% or more above ideal body weight or BMI > 30 ) (ref 1,4)
- See under 'Dose' for adjustments required in renal or hepatic impairment
Available preparations
Pancuronium bromide 4mg per 2mL ampoule
Reconstitution
Already in solution
Draw up using a 5 micron filter needle
Methods of intravenous administration
Bolus intravenous injection
- Administer required dose over a few seconds (ref 2)
- Doses as below
Dose in adults
Intubation
- Initial dose: 50 to 80 microgram/kg (intubation accomplished within 150-120 seconds), or 80 to 100 micrograms/kg (intubation accomplished within 120-90 seconds)
- Incremental doses of 10 to 20 microgram/kg may be needed
- Reduce initial dose to 20 to 60 microgram/kg in patients who have recently received suxamethonium
- See under 'Further information' for use in ICU
Obesity
- To avoid excessive dosage in obese patients, dose should be calculated on the basis of Ideal Body Weight (IBW)- see further information (ref 1)
- In obese patients, doses based on a mg/kg of actual body weight may lead to overdose
Renal impairment
- Prolonged elimination likely as pancuronium is predominantly cleared by the kidneys
- Patients with chronic renal failure may require a larger initial dose of pancuronium. A 45% increase in dose requirement has been reported in patients with end-stage renal failure (this is because of an increased volume of distribution) (ref 3)
- Recovery from neuromuscular blockade may be prolonged
Hepatic disease or biliary tract disease
- The duration of action may be prolonged. Also, resistance to neuromuscular blockade may occur because of the increased volume of distribution of the drug
- In such conditions, the drug has a slower onset, and coupled with increased dosage requirements, there may be a prolongation of blockade and recovery time in these patients
Further information
- Not used for maintenance in ICU, however doses of 60 microgram/kg up to every 60 to 90 minutes, or even less frequently, are usually adequate (ref 2)
- Licensed for administration by bolus intravenous injection only. However, it may be diluted in Sodium chloride 0.9% or Glucose 5% and administered as an infusion if required (unlicensed) (also ref 2)
- Patient is obese if actual body weight is 20% or more above ideal body weight or BMI > 30 (ref 4)Ideal body weight (IBW) calculations
- Male 50kg + (2.3 x inches over 5 feet) or 50kg + (0.9 x cm over 152 cm)
- Female 45.5kg + (2.3 x inches over 5 feet) or 45.5kg + (0.9 x cm over 152 cm)
Storage
Store between 2 and 80C
References
SPC December 2020, SPC UK March 2021 (Hospira)
1: BNF 82
2: Injectable Medicines Administration Guide UCL Hospitals 3rd edition
3: Martindale - accessed online 08/11/2021
4: Sanford guide to antimicrobial therapy (information on obesity extrapolated from data on antimicrobials)- accessed online 16/11/2021
Therapeutic classification
Muscle relaxant