Maximum Dose of Lorazepam (Ativan)
The maximum daily dose of lorazepam for adults is 10 mg/day, though the usual therapeutic range is 2-6 mg/day in divided doses, with elderly or debilitated patients requiring a maximum of only 2 mg/day. 1
Standard Adult Dosing
For anxiety disorders, the FDA-approved dosing is:
- Usual range: 2-6 mg/day in divided doses, with the largest dose at bedtime 1
- Absolute maximum: 10 mg/day 1
- Initial dosing: Most patients require 2-3 mg/day given twice or three times daily 1
For insomnia due to anxiety, a single daily dose of 2-4 mg may be given at bedtime 1
For status epilepticus in adults, the dose is 0.05-0.10 mg/kg IV (maximum 4 mg per dose), which may be repeated every 10-15 minutes if seizures continue 2. Research demonstrates that doses less than 4 mg for status epilepticus result in significantly higher progression to refractory status epilepticus (87% vs 62%), supporting the use of the full 4 mg dose 3.
PRN Dosing Guidelines
For acute anxiety or agitation, lorazepam 0.5-1 mg PRN can be given orally or IV every 4-6 hours as needed, with a maximum of 4 mg/24 hours 4. For nausea/vomiting in oncology settings, 0.5-2 mg PRN every 4-6 hours may be used 4.
Special Population Adjustments
Elderly or Debilitated Patients
Critical dose reduction is mandatory in elderly patients:
- Initial dose: 0.25-0.5 mg, with a maximum of 1-2 mg/day in divided doses 4, 1
- Absolute maximum: 2 mg/24 hours 4, 5
- Elderly patients face significantly higher risks of falls, cognitive decline, and paradoxical agitation (occurring in approximately 10% of patients) 4, 5
Hepatic Impairment
For patients with advanced liver disease, the initial dose should be reduced to 0.25 mg orally 2-3 times daily 4, 5
Frail or COPD Patients
Use lower doses of 0.25-0.5 mg, especially when combining with antipsychotics, due to increased risk of respiratory depression 4, 5
Critical Safety Warnings
Propylene glycol toxicity: Parenteral lorazepam formulations contain propylene glycol, which can cause metabolic acidosis and acute kidney injury. Total daily IV doses as low as 1 mg/kg can cause toxicity. An osmol gap greater than 10-12 mOsm/L may identify patients with significant propylene glycol accumulation 4.
Respiratory depression risk: There is an increased incidence of apnea when lorazepam is combined with other sedative agents. Monitor oxygen saturation and be prepared to provide respiratory support 2.
Paradoxical reactions: Approximately 10% of patients experience paradoxical agitation, particularly younger children and elderly patients 2, 5.
Tolerance and dependence: Regular use leads to tolerance, addiction, depression, and cognitive impairment 4, 5.
Dosing Principles
When increasing dosage, the evening dose should be increased before daytime doses 1. Dose increases should be gradual to avoid adverse effects 1.
For discontinuation, use a gradual taper to reduce withdrawal risk. If withdrawal reactions develop, pause the taper or increase back to the previous dose level, then decrease more slowly 1.
Common Pitfalls to Avoid
- Never exceed 10 mg/day in standard adults or 2 mg/day in elderly patients 1, 4
- Do not combine with other sedatives without careful monitoring, as this significantly increases respiratory depression risk 4
- Avoid chronic use beyond 2-4 weeks when possible, as benzodiazepines carry risks that outweigh benefits for long-term management 4
- Do not use as first-line for agitated delirium in elderly patients, except for alcohol or benzodiazepine withdrawal 4, 6