Benzodiazepine · Antiepileptic · Alcohol withdrawal

Lorazepam (Ativan)

Also called Ativan

Reviewed by Alex G, BSN, RN, CEN, CCRN, CMC, NREMT-P · From the Reference tab of the app

Indications

Dosing

WhereDose
Seizures and neuroLorazepam: 0.1 mg/kg IV (max 4 mg per dose), repeat once in 5–10 min
Seizures and neuroLorazepam: 0.5–2 mg IV/IM (alcohol withdrawal, stimulant toxicity)
Benzodiazepine equivalenceLorazepam: 1 mg (IV onset 5–10 min; no active metabolites)

On the quick cards

Mechanism of action

Lorazepam binds the benzodiazepine site in the GABA-A receptor's extracellular domain, between an α subunit (α1, α2, α3 or α5) and the γ2 subunit. It raises the receptor's affinity for GABA, so the chloride channel opens more often when GABA is released; without GABA it does nothing. High affinity and lower lipid solubility than diazepam mean it leaves the brain slowly, so one dose protects against seizures for hours.

Pharmacology

Pharmacokinetics

OnsetIV 5–10 min, peak sedation about 15–30 min; IM absorption is complete, peaking within 3 h (label)
DurationUsually 6–8 h (label)
Half-lifeAbout 14 h (injection label; 12 h in the oral label)
DistributionVd about 1.3 L/kg; less lipophilic than diazepam, so slower into the brain and slower out
Protein bindingAbout 91%
MetabolismDirect glucuronidation of the 3-hydroxy group to an inactive glucuronide; no CYP step, so liver disease, age and CYP drugs matter little
ClearanceAbout 1.1 mL/min/kg (label)
EliminationUrine 88%, mostly as the glucuronide
Organ failureLittle change in liver disease (label); the glucuronide accumulates in kidney failure
RoutesIV (dilute first), IM, oral and sublingual

Chemistry

Adverse effects and cautions

In the one-pagers

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Sources

  1. FDA label: Lorazepam injection (Hikma, 2021)
  2. Yahwak 2008 (osmolar gap)
  3. PubChem: lorazepam

For education and exam preparation only. Follow your institution’s protocols. Typical adult values for study. Follow the order, the label and your institution's protocols.