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pancuronium (Pavulon)

 

Classes: Neuromuscular Blockers, Nondepolarizing

Dosing and uses of Pavulon (pancuronium)

 

Adult dosage forms and strengths

injectable solution

  • 1mg/mL
  • 2mg/mL

 

General Anesthesia Adjunct/Cesarean Section

Load: 0.04-0.1 mg/kg IV

Maintenance: 0.015-0.1 mg/kg IV q30-60min Or

Continuous infusion: 0.1 mg/kg/hr IV

Dose should be calculated based on ideal body weight

Monitoring of muscle twitch response to a peripheral nerve stimulator is advised

 

Endotracheal Intubation

Bolus dose 0.06-0.1 mg/kg

Usually effective with in 2-3 minutes

 

Other Indications & Uses

Skeletal muscle relaxation during surgery, endotracheal intubation, mechanical ventilation

 

Pediatric dosage forms and strengths

injectable solution

  • 1mg/mL
  • 2mg/mL

 

Neonates (<28 Days Old)

Load: 0.02 mg/kg IV

Maintenance: 0.05-0.1 mg/kg IV q0.5-4hr PRn

 

>1 Month Old

Load: 0.04-0.1 mg/kg IV

Maintenance: 0.015-0.1 mg/kg IV q30-60min Or

Continual infusion: 0.1 mg/kg/hr IV

 

Pavulon (pancuronium) adverse (side) effects

Frequency not defined

Slight elevation in pulse rate

Elevations in blood pressure

Excessive salivation

Excessive sweating (in children)

Transient rashes

Wheezing

Dose-related tachycardia

Histamine release (bronchospasm/hypotension)

CAUTION: adequate ventilatory support mandatory, may experience resistance with >25% TBSA burns, may experience incr sensitivity w/electrolyte disorders (hyperMg, hypoK, hypoCa)

 

Warnings

Black box warnings

The drug should be administered only by adequately trained individuals familiar with its actions, characteristics, and hazards

 

Contraindications

Lack of ventilatory support, neuromuscular disease

Hypersensitive to drug &/or bromides

 

Cautions

Additive/synergistic effects if administered with or following an opioid, sedative or anesthetic agent

In pts with poor renal perfusion or severe renal disease, preexisting tachycardia

Severe anaphylactic reactions to neuromuscular blocking agents have been reported; these reactions have, in some cases, been life threatening and fatal; because of the potential severity of these reactions, the necessary precautions, such as the immediate availability of appropriate emergency treatment, should be taken

 

Pregnancy and lactation

Pregnancy category: C

Lactation: not known if excreted in breast milk; effect on nursing infant not known

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Pavulon (pancuronium)

Half-Life:

2 hr (terminal phase)

Renal dysfunction may incr half-life 50%

 

Other Information

Onset: 1-2 min

Duration: 60 min

Protein Bound: 87% (range: 77-91%)

Metabolism: primarily none, some hepatic transformation to weakly active metabolite

Excretion: unchanged in urine

Little effect on intraocular/intracranial pressure

Very rarely causes release of histamine (and hypotension, bronchospasm, flushing); more commonly causes dose-related tachycardia by blocking cardiac ACh receptors

 

Mechanism of action

Non-depolarizing skeletal muscle relaxant; cholinergic receptor antagonist

 

Administration

IV Compatibilities

Additive: ciprofloxacin, verapamiL

Syringe: caffeine, heparin

Y-site: aminophylline, cefazolin, cefuroxime, cimetidine, dobutamine, dopamine, epinephrine, esmolol, etomidate, fenoldopam, fentanyl, fluconazole, gentamicin, heparin, Hextend, hydrocortisone, isoproterenol, levofloxacin, lorazepam, midazolam, milrinone, morphine, nitroglycerin, propofol (1 mg/mL), ranitidine, Na nitroprusside, trimethoprim/sulfamethoxazole, vancomycin

 

IV Incompatibilities

Y-site: diazepam, thiopentaL

 

IV Preparation

Solution: add to an empty Viaflex bag & infuse undiluted (2 mg/mL); however, if necessary, may be diluted in D5W, NS, or Lr

Continuous infusions may be given by using undiluted drug

 

IV Administration

Use controlled microinfusion device

 

Storage

Store at 2-8 C; stable at RT x 6mth