(Bold for FDA approved)
• May bind selectively to a subtype of the benzodiazepine receptor, the alpha 1 isoform
• May enhance GABA inhibitory actions that provide sedative hypnotic effects more selectively than other actions of GABA
• Boosts chloride conductance through GABA-regulated channels
• Inhibitory actions in sleep centers may provide sedative hypnotic effects
• Generally takes effect in less than an hour
• Unpleasant taste
• Sedation
• Dizziness
• Dose-dependent amnesia
• Nervousness
• Dry mouth, headache
• Respiratory depression, especially when taken with other CNS depressants in overdose
• Rare angioedema
unusual
common
• Wait
• To avoid problems with memory, take eszopiclone only if planning to have a full night’s sleep
• Lower the dose
• Switch to a shorter-acting sedative hypnotic
• Administer flumazenil if side effects are severe or life-threatening
• 2–3 mg at bedtime
• Tablet 1 mg, 2 mg, 3 mg
• No development of tolerance was seen in studies up to 6 months
• Eszopiclone is a Schedule IV drug
• Some patients could develop dependence and/or tolerance with drugs of this class; risk may be theoretically greater with higher doses
• History of drug addiction may theoretically increase risk of dependence
• Dose adjustment not generally necessary
• Dose adjustment not generally recommended for mild-to-moderate hepatic impairment
• For severe impairment, recommended initial dose 1 mg at bedtime; maximum dose 2 mg at bedtime
• Dosage adjustment may not be necessary
• May be more susceptible to adverse effects
• Initial dose 1 mg at bedtime; maximum dose generally 2 mg at bedtime
• Safety and efficacy have not been established
• Long-term effects of eszopiclone in children/adolescents are unknown
• Should generally receive lower doses and be more closely monitored
• Effective June 30, 2015, the FDA requires changes to the content and format of pregnancy and lactation information in prescription drug labels, including the elimination of the pregnancy letter categories; the Pregnancy and Lactation Labeling Rule (PLLR or final rule) applies only to prescription drugs and will be phased in gradually for drugs approved on or after June 30, 2001
• Controlled studies have not been conducted in pregnant women
• Infants whose mothers took sedative hypnotics during pregnancy may experience some withdrawal symptoms
• Neonatal flaccidity has been reported in infants whose mothers took sedative hypnotics during pregnancy
• Unknown if eszopiclone is secreted in human breast milk, but all psychotropics are assumed to be secreted in breast milk
• Recommended either to discontinue drug or bottle feed
Based on data Published online by Cambridge University Press
Compiled by Dr. Jash Ajmera