(ve-cure-oh-nee-yum) ,


(trade name)


Therapeutic: neuromuscular blocking agents nondepolarizing
Pregnancy Category: C


Induction of skeletal muscle paralysis and facilitation of intubation after induction of anesthesia in surgical procedures.Facilitation of compliance during mechanical ventilation.


Prevents neuromuscular transmission by blocking the effect of acetylcholine at the myoneural junction. Has no analgesic or anxiolytic properties

Therapeutic effects

Skeletal muscle paralysis.


Absorption: Following IV administration, absorption is essentially complete.
Distribution: Rapidly distributes in extracellular fluid; minimal penetration of the CNS.
Metabolism and Excretion: Some metabolism by the liver (20%), with conversion to at least one active metabolite; 35% excreted unchanged by the kidneys
Half-life: Infants: 65 min; Children: 41 min; Adults: 65–75 min (↓ near term in pregnant patients, ↑ in hepatic impairment).

Time/action profile

IV1–3 min3–5 min30–40 min


Contraindicated in: Hypersensitivity; Hypersensitivity to bromides;
Use Cautiously in: Dehydration or electrolyte abnormalities (should be corrected); Fractures or muscle spasm; Hyperthermia (↑ duration/intensity of paralysis); Significant hepatic impairment; Shock; Extensive burns (may be more resistant to effects); Low plasma pseudocholinesterase levels (may be seen in association with anemia, dehydration, cholinesterase inhibitors/insecticides, severe liver disease, pregnancy, or hereditary predisposition); Obese patients ; Obstetric / Lactation: Safety not established (use only if benefit outweighs potential risk to fetus) Pediatric: Children <7 wk (safety and effectiveness not established)
Exercise Extreme Caution in: Neuromuscular diseases such as myasthenia gravis (small test dose may be used to assess response).

Adverse Reactions/Side Effects


  • bronchospasm


  • rash


  • allergic reactions including anaphylaxis (life-threatening)


Drug-Drug interaction

Intensity and duration of paralysis may be prolonged by pretreatment with succinylcholine, general anesthesia (inhalation), aminoglycosides, vancomycin, tetracyclines, polymyxin B, colistin, clindamycin, lidocaine, and other local anesthetics, lithium, quinidine, procainamide, beta-adrenergic blocking agents, potassium-losing diuretics, or magnesium.Higher infusion rates may be required and duration of action may be shortened in patients receiving long-term carbamazepine or phenytoin.


Intravenous (Adults and Children >10 yr) Intubation—0.08–0.1 mg/kg (0.06–0.085 mg/kg if given after steady-state anesthesia achieved or 0.04–0.06 mg/kg after succinylcholine-assisted intubation and anesthesia; wait for disappearance of succinylcholine effects; or 0.05–0.06 mg/kg during balanced anesthesia); Maintenance dose—0.01–0.015 mg/kg 25–40 min after initial dose, then q 12–15 min as needed; Continuous infusion— 0.8–1.2 mcg/kg/min.
Intravenous (Children 1–10 yr) 0.1 mg/kg q 1 hr as needed.
Intravenous (Infants 7 wk– 1 yr) 0.1 mg/kg q 1 hr as needed or as a continuous infusion of 1–1.5 mcg/kg/min.

Availability (generic available)

Powder for injection: 10 mg/vial, 20 mg/vial

Nursing implications

Nursing assessment

  • Assess respiratory status continuously throughout therapy with vecuronium. Should be used only to facilitate intubation or in patients already intubated.
  • Neuromuscular response should be monitored with a peripheral nerve stimulator intraoperatively. Paralysis is initially selective and usually occurs sequentially in the following muscles: levator muscles of eyelids, muscles of mastication, limb muscles, abdominal muscles, muscles of the glottis, intercostal muscles, and the diaphragm. Recovery of muscle function usually occurs in reverse order.
  • Monitor ECG, heart rate, and BP throughout administration.
  • Observe for residual muscle weakness and respiratory distress during the recovery period.
  • Monitor infusion site frequently. If signs of tissue irritation or extravasation occur, discontinue and restart in another vein.
  • If overdose occurs, use peripheral nerve stimulator to determine the degree of neuromuscular blockade. Maintain airway patency and ventilation until recovery of normal respirations occurs.
    • Administration of anticholinesterase agents (neostigmine, pyridostigmine) may be used to antagonize the action of neuromuscular blocking agents once the patient has demonstrated some spontaneous recovery from neuromuscular block. Atropine is usually administered prior to or concurrently with anticholinesterase agents to counteract the muscarinic effects.
    • Administration of fluids and vasopressors may be necessary to treat severe hypotension or shock.

Potential Nursing Diagnoses

Ineffective breathing pattern (Indications)
Impaired verbal communication (Side Effects)
Fear (Side Effects)


  • high alert: Unplanned administration of a neuromuscular blocking agent instead of administration of the intended medication or administration of a neuromuscular blocking agent in the absence of ventilatory support has resulted in serious harm and death. Confusing similarities in packaging and insufficiently controlled access to these medications are often implicated in these medication errors.
  • Dose is titrated to patient response.
    • Vecuronium has no effect on consciousness or pain threshold. Adequate anesthesia/analgesia should always be used when vecuronium is used as an adjunct to surgical procedures or when painful procedures are performed. Benzodiazepines and/or analgesics should be administered concurrently when prolonged vecuronium therapy is used for ventilator patients, because patient is awake and able to feel all sensations.
    • If eyes remain open throughout prolonged administration, protect corneas with artificial tears.
    • Store in refrigerator.
    • Most neuromuscular blocking agents are incompatible with barbiturates and sodium bicarbonate. Do not admix.
  • Intravenous Administration
  • Intravenous: Reconstitute with bacteriostatic water (may be provided by manufacturer), D5W, 0.9% NaCl, D5/0.9% NaCl, or LR injection. Solution reconstituted with bacteriostatic water is stable if refrigerated for 5 days. If other diluents are used, solution is stable for 24 hr if refrigerated. Discard all unused solution.
  • Concentration: Maximum of 2 mg/ml. Titrate dose according to patient response.
  • Continuous Infusion: Diluent: Dilute to a concentration of 1 mg/ml in D5W, 0.9% NaCl, or LR. Use sterile water for injection instead of manufacturer-provided diluent (contains benzyl alcohol) when reconstituting for use in neonates.
  • Rate: Titrate rate of infusion according to patient response.
  • Y-Site Compatibility: alemtuzumab, alfentanil, alprostadil, amifostine, amikacin, aminophylline, amiodarone, ampicillin, ampicillin/sulbactam, anidulafungin, argatroban, azithromycin, aztreonam, bivalirudin, bleomycin, bumetanide, buprenorphine, butorphanol, calcium chloride, calcium gluconate, carboplatin, carmustine, caspofungin, cefazolin, cefotetan, cefoxitin, ceftazidime, ceftriaxone, cefuroxime, chlorpromazine, ciprofloxacin, cisplatin, clindamycin, cyclophosphamide, cyclosporine, cytarabine, dactinomycin, daptomycin, dexamethasone sodium phosphate, dexmedetomidine, dexrazoxane, digoxin, diltiazem, diphenhydramine, dobutamine, docetaxel, dolasetron, dopamine, doxorubicin hydrochloride, doxorubicin liposomal, doxycycline, droperidol, enalaprilat, ephedrine, epinephrine, epirubicin, eptifibatide, ertapenem, erythromycin, esmolol, etoposide, etoposide phosphate, famotidine, fenoldopam, fentanyl, fluconazole, fludarabine, fluorouracil, foscarnet, gemcitabine, gentamicin, glycopyrrolate, granisetron, haloperidol, heparin, hydralazine, hydrocortisone sodium succinate, hydromorphone, idarubicin, ifosfamide, insulin, irinotecan, isoproterenol, labetalol, leucovorin calcium, levofloxacin, lidocaine, linezolid, lorazepam, magnesium sulfate, mannitol, mechlorethamide, melphalan, meperidine, meropenem, methotrexate, methyldopate, metoclopramide, metoprolol, metronidazole, midazolam, milrinone, mitoxantrone, morphine, moxifloxacin, mycophenolate, nalbuphine, naloxone, nesiritide, nicardipine, nitroglycerin, nitroprusside, norepinephrine, octreotide, ondansetron, oxaliplatin, paclitaxel, palonosetron, pamidronate, pemetrexed, pentazocine, pentobarbital, phenobarbital, phenylephrine, potassium acetate, potassium chloride, potassium phosphates, procainamide, prochlorperazine, promethazine, propranolol, quinupristin/dalfopristin, ranitidine, remifentanil, sodium acetate, sodium bicarbonate, sodium phosphates, streptozocin, succinylcholine, sufentanil, tacrolimus, teniposide, theophylline, thiotepa, ticarcillin/clavulanate, tigecycline, tirofiban, tobramycin, trimethoprim/sulfamethoxazole, vancomycin, vasopressin, verapamil, vinblastine, vincristine, vinorelbine, voriconazole, zidovudine, zolendronic acid
  • Y-Site Incompatibility: acyclovir, allopurinol, amphotericin B cholesteryl, amphotericin B colloidal, amphotericin B lipid complex, amphotericin B liposome, busulfan, cefepime, cefotaxime, chloramphenicol, dantrolene, diazepam, etomidate, furosemide, ganciclovir, ibuprofen, imipenem/cilastatin, ketorolac, methohexital, methylprednisolone sodium succinate, micafungin, nafcillin, pantoprazole, pentamidine, phenytoin, piperacillin/tazobactam, thiopental

Patient/Family Teaching

  • Explain all procedures to patient receiving vecuronium therapy without general anesthesia, because consciousness is not affected by vecuronium alone.
  • Reassure patient that communication abilities will return as medication wears off.

Evaluation/Desired Outcomes

  • Adequate suppression of the twitch response when tested with peripheral nerve stimulation and subsequent muscle paralysis.
  • Improved compliance during mechanical ventilation.
Drug Guide, © 2015 Farlex and Partners


A brand name for VECTURONIUM.
Collins Dictionary of Medicine © Robert M. Youngson 2004, 2005
References in periodicals archive ?
Genel anestezi induksiyonunda 5 mg [kg.sup.-1] tiyopental (Pental 0,5 gr flakon, Ibrahim Ethem Ulagay, Turkiye) ve 0,1 mg [kg.sup.-1] vekuronyum (Norcuron flakon, MSD, USA) yapildi ve hastalar entube edildi.
Subsequent testing showed positive reaction to atropine, Dormicum, Esmeron, Lysthenon, Norcuron and Rapifen.
Clinical pharmacology of Org NC45 (Norcuron): A new nondepolarizing muscle relaxant.
Sample Collection and Storage: After overnight fasting animals were anaesthetized with Norcuron (150 l/100gof body weight) blood samples were collected in serum gel vaccutainers directly by cardiac puncture.
He was given medications, including Norcuron, Versed, and Ativan, which rendered him motionless.
Rocuronium and vecuronium are marketed in Europe under the trade names ESMERON and NORCURON, respectively.
The nurse obtained and administered the neuromuscular blocking agent vecuronium (Norcuron) instead, which led to a fatal heart arrhythmia.
"The names NARCAN (naloxone) and NORCURON (vecuronium) look alike when orders are handwritten and sound alike when orders are transmitted verbally.
Norcuron is included to finalize the euthanizing act for the remaining 10 percent.
After several failed attempts, the patient was at last weaned from the ventilator and given doses of morphine and Versed, standard medications in the palliative procedure known as "terminal sedation." To these drugs Thompson added a third, a neuromuscular blocking agent called Norcuron. The patient died soon thereafter in 2002.
Two anaesthetic drugs, propofol (Fresofol [R], Fresenius Kabi Austria GmbH, Graz, Austria), and vecuronium (Norcuron [R], N.V.