
Survec10 mg/vial
Healthcare Pharmaceuticals Ltd.
Vecuronium Bromide is an FDA-approved, established treatment indicated as an adjunct to general anesthesia for the following uses: Facilitation of endotracheal intubation: Vecuronium Bromide is used…
Vecuronium Bromide is an FDA-approved, established treatment indicated as an adjunct to general anesthesia for the following uses:
Vecuronium Bromide has no sedative, analgesic, or anesthetic properties of its own and must always be given together with adequate general anesthesia or sedation and analgesia.
Vecuronium Bromide is administered only as an intravenous injection or infusion by, or under the direct supervision of, an anesthesiologist or clinician experienced in the use of neuromuscular blocking agents and airway management, with facilities for immediate tracheal intubation and mechanical ventilation available at all times.
| Purpose | Dose | Notes |
|---|---|---|
| Initial (intubating) dose | 0.08-0.1 mg/kg IV bolus | Produces intubation conditions in approximately 2.5-3 minutes |
| Initial dose with prior succinylcholine | 0.04-0.06 mg/kg IV | Provides approximately 25-40 minutes of muscle relaxation |
| Initial dose with volatile (inhalation) anesthetics | Reduced by approximately 15% (0.06-0.085 mg/kg) | Volatile anesthetics potentiate neuromuscular blockade |
| Maintenance dose | 0.01-0.015 mg/kg IV | Given at approximately 12-15 minute intervals, guided by twitch response monitoring |
| Continuous IV infusion | Approximately 0.8-1.2 mcg/kg/min (range up to 1.4 mcg/kg/min) | Initiated after early spontaneous recovery from an initial bolus, titrated to maintain the desired degree of twitch suppression |
Dosing should always be individualized and guided by peripheral nerve stimulator (twitch) monitoring where available. See Reconstitution for preparation instructions and Use in Special Populations for dosing in obesity and other conditions.
The most significant risk associated with Vecuronium Bromide is an extension of its expected pharmacological action beyond the period needed, resulting in prolonged skeletal muscle weakness or paralysis, including of the respiratory muscles, which can lead to respiratory insufficiency or apnea if not properly managed with ventilatory support.
Other reported side effects include:
Rare but serious: severe anaphylactic or anaphylactoid reactions, which can be life-threatening, have been reported with Vecuronium Bromide and other neuromuscular blocking agents. Prolonged use in the intensive care unit has been associated with prolonged muscle weakness, myopathy, and muscle atrophy that may take an extended period to resolve.
Vecuronium Bromide is contraindicated in patients with a known history of hypersensitivity to vecuronium bromide or the bromide ion. There are no other well-established absolute contraindications to Vecuronium Bromide; conditions such as hepatic/renal impairment, myasthenia gravis, electrolyte imbalance, and obesity are important precautions requiring dose adjustment and enhanced monitoring rather than absolute contraindications (see Precautions and Warnings).
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