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Vecuronium bromide injection

Presentation

Powder for solution for injection containing vecuronium bromide.

Drugs List

  • vecuronium bromide 10mg powder for solution for injection vial
  • Therapeutic Indications

    Uses

    Neuromuscular blockade to facilitate intubation during surgery

    An adjunct to general anaesthesia to facilitate tracheal intubation and skeletal muscle relaxation during surgery.

    Dosage

    Individual requirements vary and the recommended dosages are only a guide.

    The anaesthetic method used, the expected duration of surgery, the concomitant medication used and the patient condition should be taken into account when determining the dose.

    The use of an appropriate neuromuscular monitoring technique is recommended to monitor neuromuscular block and recovery.

    Adults

    Tracheal intubation
    Loading dose
    80micrograms/kg to 100micrograms/kg by intravenous injection.

    Maintenance
    20micrograms/kg to 30micrograms/kg by intravenous injection, to be given when twitch height has recovered to 25% of control twitch height.
    Alternatively, 0.8micrograms/kg/minute to 1.4micrograms/kg/minute by continuous intravenous infusion can be used to maintain neuromuscular block. Monitoring of neuromuscular block is recommend as infusion rate requirements vary in individual patients.

    Surgical procedures after intubation with suxamethonium
    If suxamethonium is used for intubation, the administration of vecuronium bromide should be delayed until the patient has recovered from the neuromuscular block induced by suxamethonium.
    Maintenance
    30micrograms/kg to 50micrograms/kg.

    Children

    Children aged 12 to 18 years
    Tracheal intubation
    Loading dose
    80micrograms/kg to 100micrograms/kg by intravenous injection.

    Maintenance
    20micrograms/kg to 30micrograms/kg by intravenous injection, to be given when twitch height has recovered to 25% of control twitch height.

    Children aged 2 to 12 years
    Dose requirements in children are higher than for adults and neonates. However, the same loading and maintenance doses by intravenous injection are usually sufficient. See Dosage; Adult.

    The duration of action is shorter in children, maintenance doses are required more frequently.

    Children aged 4 months to 2 years
    The onset time of vecuronium bromide in patients in this age group is shorter in comparison to adults and older children. The use of high intubating doses in general are not required for early development of good intubating conditions.
    The duration of action is shorter in children, maintenance doses are required more frequently. However, the dose requirements by intravenous injection are the same as adults. See Dosage; Adult.

    Neonates from birth up to 4 months of age
    Initial
    As sensitivity of the neuromuscular junction may vary, an initial test dose of 10micrograms/kg to 20micrograms/kg is recommended. Followed by incremental doses until 90 to 95% depression of twitch response is achieved.
    Maximum dose 100micrograms/kg.

    Administration

    To be administered by intravenous bolus injection or in adults only by a continuous intravenous infusion.

    Contraindications

    None known

    Precautions and Warnings

    Burns
    Cachexia
    Children under 4 months
    Elderly
    Hypoproteinaemia
    Hypothermia
    Obesity
    Oedema
    Biliary tract disorder
    Breastfeeding
    Cardiovascular disorder
    Dehydration
    Electrolyte imbalance
    Hepatic impairment
    Hypercapnia
    Hypermagnesaemia
    Hypocalcaemia
    Hypokalaemia
    Metabolic acidosis
    Myasthenia gravis
    Myasthenic Eaton-Lambert syndrome
    Neuromuscular disorder
    Poliomyelitis
    Pregnancy
    Renal impairment

    Correct existing water and electrolyte disturbances before administration
    Resuscitation facilities must be immediately available
    To be administered by anaesthetist or a doctor trained in intensive care
    Ventilatory support is mandatory until adequate respiration is restored
    Monitor neuromuscular function
    Neonates are particularly sensitive to non-depolarising NMBDs
    May cause anaphylactic / anaphylactoid reactions
    Burns patients may require dose modification
    In obese patients dosing should be based on ideal weight
    Driving or operating machinery not advisable following treatment

    Pregnancy and Lactation

    Pregnancy

    Use vecuronium bromide with caution during pregnancy.

    The manufacturer states that vecuronium bromide should only be used in pregnancy if the potential benefits outweigh the potential risks.

    Briggs (2015) state that the use of vecuronium bromide during pregnancy has not been shown to result in any adverse effects on pregnancy rate, the foetus or the newborn. Due to the lack of animal studies using vecuronium bromide during pregnancy, a risk to the embryo during organogenesis cannot be excluded.

    Studies with vecuronium bromide, administered in doses up to 100micrograms/kg, have shown its safety for use in caesarean section. In caesarean section the dose should not exceed 100micrograms/kg. In several clinical studies vecuronium bromide did not affect Apgar score, foetal muscle tonus or cardiorespiratory adaptation. Umbilical cord blood sampling shows that very little placental transfer of vecuronium bromide occurs, and no clinical adverse effects in the newborn were reported.

    Lactation

    Use vecuronium bromide with caution during breastfeeding.

    The manufacturer recommends to decide whether to discontinue the use of vecuronium bromide or breastfeeding during treatment with vecuronium bromide. Taking into account the potential benefits and risks to the mother and infant.

    It is unknown if vecuronium bromide is excreted into breast milk. No animal studies have been performed.

    Briggs (2015) states that it is unlikely that clinically significant amounts of vecuronium bromide would be excreted into breast milk. Vecuronium bromide's relatively low molecular weight and it's low lipid solubility would inhibit its excretion into breast milk, therefore Briggs (2015) suggests a lack of risk to breastfed infants.

    Side Effects

    Anaphylactic reaction
    Anaphylactic shock
    Anaphylactoid reaction
    Angioedema
    Apnoea
    Bronchospasm
    Cardiovascular disturbances
    Circulatory collapse
    Erythema at injection site
    Erythematous rash
    Facial oedema
    Flushing
    Hypersensitivity reactions
    Hypotension
    Injection site reactions
    Itching (injection site)
    Local pain (injection site)
    Muscle weakness
    Myopathy
    Paralysis
    Rash
    Respiratory insufficiency
    Shock
    Tachycardia
    Urticaria

    Overdosage

    It is strongly recommended that the UK National Poisons Information Service be consulted on cases of suspected or actual overdose where there is doubt over the degree of risk or about appropriate management.

    The following number will direct the caller to the relevant local centre (0844) 892 0111

    Information may be obtained if you have access to ToxBase the primary clinical toxicology database of the National Poisons Information Service. This is available via password on the internet ( www.toxbase.org ) or if this is unavailable at the backup site ( www.toxbasebackup.org ).

    Further Information

    Last Full Review Date: March 2019

    Reference Sources

    Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk, 10th edition (2015) ed. Briggs, G., Freeman, R. Wolters Kluwer Health, Philadelphia.

    Summary of Product Characteristics: Vecuronium bromide 10mg powder for solution for injection. Kent Pharmaceuticals Ltd. Revised February 2016.

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