Sevoflurane

DEA Class;  Rx

Common Brand Names; Ultane

  • General Anesthetics, Inhalation

Halogenated general anesthetic; depth of anesthesia is easily adjusted; induction and recovery from anesthesia is rapid; cardiorespiratory depression is minimal; generally safe in patients with coronary artery disease; appropriate for pediatric patients

Indicated For use in general anesthesia induction during inpatient or outpatient surgery.

For general anesthesia maintenance during inpatient or outpatient surgery.

Known or suspected genetic susceptibility to malignant hyperthermia

Known or suspected sensitivity to sevoflurane or to other halogenated inhalational anesthetics

  • Malignant hyperthermia
  • Dose-dependent hypotension
  • Bradycardia
  • Tachycardia
  • Hypotension
  • Hypertension
  • Nausea/vomiting
  • Cough
  • Agitation
  • Increased salivation
  • Airway obstruction
  • Laryngospasm
  • Apnea
  • Increased BUN
  • Increased ALT
  • Respiratory irritation
  • Nephrotoxicity
  • Glycosuria
  • Proteinuria
  • Seizures (majority of cases in children and young adults, most had no medical history of seizures)
  • Cardiac arrest
  • Cases of mild, moderate and severe post-operative hepatic dysfunction or hepatitis with or without jaundice
  • Malignant hyperthermia
  • Allergic reactions (eg, rash, urticaria, pruritus, bronchospasm, anaphylactic or anaphylactoid reactions)
  • Transient elevations in glucose, liver function tests, and WBC count
  • Bradycardia in patients with Down syndrome

Volatile liquid; use appropriate vaporizer for inhalation

Agitation/delirium may occur

Postoperative hepatitis reported

Closely monitor patients with anemia, hepatic impairment, myxedema, renal impairment

Can induce malignant hyperthermia in genetically susceptible individuals

Advise patients that performance of activities requiring mental alertness, such as driving or operating machinery, may be impaired after sevoflurane anesthesia

Reports of QT prolongation, associated with torsade de pointes (in exceptional cases, fatalities reported); exercise caution when administering to susceptible patients (eg, congenital long QT syndrome, coadministration with drugs that prolong QT interval)

Should not be used as a sole agent of induction in patients with ventricular dysfunction

Risk of perioperative hyperkalemia in pediatric patients reported (rare); some resulting in cardiac arrhythmia and death

There are no adequate and well-controlled studies in pregnant women; in animal reproduction studies, reduced fetal weights were noted following exposure to 1 MAC sevoflurane for three hours a day during organogenesis

The concentrations of sevoflurane in milk are probably of no clinical importance 24 hours after anesthesia; because of rapid washout, sevoflurane concentrations in milk are predicted to be below those found with many other volatile anesthetics

Adults

Specific maximum dosage information is not available. Dosage must be individualized.

Elderly

Specific maximum dosage information is not available. Dosage must be individualized.

Adolescents

Specific maximum dosage information is not available. Dosage must be individualized.

Children

Specific maximum dosage information is not available. Dosage must be individualized.

Sevoflurane

liquid

  • 100%

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