Sedative-hypnotic agents are used widely for the treatment of anxiety and insomnia. As a group, they are one of the most frequently prescribed medications. Barbiturates (See Barbiturates), benzodiazepines (See Benzodiazepines), antihistamines (See Antihistamines), skeletal muscle relaxants (See Skeletal Muscle Relaxants), antidepressants (See Antidepressants, General (Noncyclic) and Antidepressants, Tricyclic), and anticholinergic agents (See Anticholinergics) are discussed elsewhere in this book. This section and Table II–53 list some of the less commonly used hypnotic agents.
Table II-53 Sedative-Hypnotic Agentsa |Favorite Table|Download (.pdf)
Table II-53 Sedative-Hypnotic Agentsa
Usual Adult Oral Hypnotic Dose (mg)
Approximate Lethal Dose (g)
Toxic Concentration (mg/L)
Usual Half–lifeb (h)
Mechanism of toxicity. The exact mechanism of action and the pharmacokinetics (see Table II–61) vary for each agent. The major toxic effect that causes serious poisoning or death is CNS depression resulting in coma, respiratory arrest, and pulmonary aspiration of gastric contents.
Toxic dose. The toxic dose varies considerably between drugs and also depends largely on individual tolerance and the presence of other drugs, such as alcohol. For most of these drugs, ingestion of 3–5 times the usual hypnotic dose results in coma. However, co-ingestion of alcohol or other drugs may cause coma after smaller ingestions, whereas individuals who chronically use large doses of these drugs may tolerate much higher acute doses.
Clinical presentation. Overdose with any of these drugs may cause drowsiness, ataxia, nystagmus, stupor, coma, and respiratory arrest. Deep coma may result in absent reflexes, fixed pupils, and depressed or absent electroencephalographic (EEG) activity. Hypothermia is common. Most of these agents also slow gastric motility and decrease muscle tone. Hypotension with a large overdose is caused primarily by depression of cardiac contractility and, to a lesser extent, loss of venous tone.
is metabolized to trichloroethanol, which also has CNS-depressant activity. In addition, trichloroethanol may sensitize the myocardium to the effects of catecholamines, resulting in cardiac arrhythmias.
may cause nausea, vomiting, drowsiness, and miosis. There have been no reported deaths.
Ethchlorvynol has a pungent odor, sometimes described as pearlike, and gastric fluid often has a pink or green color, depending on the capsule form (200- and 500-mg capsules are red; 750-mg capsules are green).
Glutethimide often produces mydriasis (dilated pupils) and other anticholinergic side effects, and patients may exhibit prolonged and cyclic or fluctuating ...