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atracurium (Tracurium)

Tradename: Tracurium. Indications: 1) to skeletal muscle relaxation during surgery 2) to increase pulmonary compliance during ventilator-assisted respiration 3) status asthmaticus refractory to other treatment 4) must always be used with a sedative (benzodiazepine) 5) should be used with an analgesic Dosage: 1) bolus: 0.4-0.5 mg/kg IV. 2) maintenance 2-10 ug/kg/min (0.4-0.8 mg/kg/hr) Injection: 10 mg/mL (10 mL) Dosage adjustment in renal failure: not needed Pharmacokinetics: 1) onset of action is within 2 minutes (IV) 2) maximal effects seen in 3-5 minutes (IV) 3) duration 20-30 min 4) non-enzymatic degradation in blood stream 5) further metabolism by plasma esterases 6) major metabolite laudanosine accumulates with renal failure 7) eliminated in urine & feces Adverse effects: 1) not common (1-10%) - flushing, generally mild & due to histamine release 2) uncommon (< 1%) a) muscle weakness, bradycardia/tachycardia, erythema at site of injection, increased risk of DVT, prolonged paralysis, salivation, potentiation of adverse effects of hyperkalemia or hypokalemia b) laudanosine accumulation is associated with hypotension, excitation & possibly seizures Drug interactions: 1) coadministration of aminoglycosides, tetracyclines or clindamycin prolongs & increased neuromuscular blockade 2) coadministration of corticosteroids prolongs muscle weakness 3) K+ depleting agents (thiazides, loop diuretics, amphotericin B, corticosteroids) can increase & prolong neuromuscular paralysis 4) reduce dosage by 33% in patients receiving isoflurane or enflurane 5) reduce by 20% in patients receiving halothane Reversal: 1) neostygmine, pyridostigmine, edrophonium, cholinesterase inhibitors are used with atropine to reverse neuromuscular blockade 2) neostigmine 1-3 mg slow IV push (0.5 mg in child) with or immediately after atropine 1-1.5 mg IV push Mechanism of action: 1) intermediate-acting, non-depolarizing neuromuscular junction blocker 2) skeletal muscle relaxation produced by diminished response to acetylcholine at the neuromuscular junction 3) block access of acetylcholine to motor end-plate

Interactions

drug interactions

General

aromatic compound heterocyclic compound, 2 rings neuromuscular blocker (paralyzing agent)

Properties

MISC-INFO: elimination route PLASMA pregnancy-category C safety in lactation ?

Database Correlations

PUBCHEM correlations

References

  1. Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed. Gilman et al, eds. Permagon Press/McGraw Hill, 1990, pg 169
  2. Drug Information & Medication Formulary, Veterans Affairs, Central California Health Care System, 1st ed., Ravnan et al eds, 1998 - not on National VA formulary
  3. Kaiser Permanente Northern California Regional Drug Formulary, 1998
  4. Deprecated Reference