Menu

Lorazepam

Brand namesAtivan

Lorazepam is used to treat anxiety disorders and short-term anxiety relief. It is available as Ativan and is commonly prescribed in the mental health category.

Reviewed by Zimmer Medical GroupUpdated 8 min read

About Lorazepam

Lorazepam is a short-to-intermediate-acting benzodiazepine (gaba-a receptor modulator) also known by the brand name Ativan. It is primarily used to is prescribed to treat: • Anxiety disorders and short term anxiety relief • Various related conditions in the mental health category • Associated symptoms and complications It is an important medication that helps manage these conditions effectively. Lorazepam is available in oral tablet (0.5 mg, 1 mg, 2 mg), oral concentrate solution (2 mg/ml), iv / im injection (2 mg/ml, 4 mg/ml), and sublingual tablet (1 mg, 2 mg) form. Healthcare providers commonly prescribe Lorazepam for conditions including Generalized Anxiety Disorder (GAD).

Lorazepam at a Glance

Brand names
Ativan
Drug class
Short-to-Intermediate-Acting Benzodiazepine (GABA-A Receptor Modulator)
DEA schedule
Schedule Schedule IV (controlled substance)
Pregnancy category
FDA Category Category D — Use during the first trimester has been associated with an increased risk of congenital malformations, including oral cleft. Use late in pregnancy may cause neonatal sedation, hypotonia, feeding difficulties, and withdrawal. Use during pregnancy only if the potential benefit clearly justifies the risk to the fetus.
Available forms
Oral tablet (0.5 mg, 1 mg, 2 mg), Oral concentrate solution (2 mg/mL), IV / IM injection (2 mg/mL, 4 mg/mL), Sublingual tablet (1 mg, 2 mg)
Therapeutic categories
Mental Health, Benzodiazepines, Anxiety
Conditions treated
1 related condition on this site

What Lorazepam Is Used For

is prescribed to treat:

Anxiety disorders and short-term anxiety relief • Various related conditions in the mental health category • Associated symptoms and complications

It is an important medication that helps manage these conditions effectively.

Dosage Quick Reference

These are general dosage guidelines for Lorazepam. Your doctor will determine the appropriate dose for your specific situation.

ConditionStarting DoseMaintenance Dose
Anxiety (adults)1–2 mg/day in 2–3 divided doses2–6 mg/day in divided doses; max 10 mg/day
Insomnia from anxiety2–4 mg orally at bedtimeShort-term use; reassess in 7–10 days
Status epilepticus (IV)4 mg IV over 2 minutesMay repeat 4 mg IV in 10–15 minutes; max 8 mg in 12 hours
Pre-procedural sedation (IM)0.05 mg/kg IM, max 4 mgSingle dose 2 hours before procedure
Older adults / debilitated patients0.5–1 mg/day in divided dosesTitrate slowly; max 2 mg/day initially

Side Effects

Common side effects may include:

Nausea or stomach upset • Headache • Dizziness or lightheadedness • Fatigue or tiredness • Mild rash or itching

Serious side effects (seek immediate medical attention):

• Severe allergic reactions (rash, hives, swelling, difficulty breathing) • Unusual bleeding or bruising • Severe stomach pain • Signs of liver problems (yellowing of skin/eyes, dark urine) • Chest pain or irregular heartbeat • Severe dizziness or fainting • Signs of serious adverse effects

See also: Drug Interactions ↓

Drug Interactions

Lorazepam is metabolized by glucuronidation rather than CYP450 enzymes, which means it has fewer pharmacokinetic interactions than many other benzodiazepines. The most important interactions are pharmacodynamic.

  • Opioids (e.g., oxycodone, hydrocodone, morphine, fentanyl, tramadol): Profound sedation, respiratory depression, coma, and death. An FDA Boxed Warning applies. Avoid co-prescription when possible; if combined, use the lowest effective doses for the shortest duration with close monitoring.
  • Other CNS depressants (alcohol, sedating antihistamines, gabapentinoids, muscle relaxants, sleep aids): Additive sedation, impaired psychomotor performance, falls, and respiratory depression. Counsel against alcohol and recreational sedatives.
  • Clozapine: Rare reports of severe respiratory depression, hypotension, and cardiorespiratory arrest when combined with parenteral lorazepam. Avoid IV/IM lorazepam in patients on clozapine.
  • Probenecid and valproate: Inhibit lorazepam glucuronidation, increasing lorazepam levels and prolonging effects. Reduce lorazepam dose by approximately 50 percent.
  • Theophylline and aminophylline: May antagonize the sedative effects of lorazepam, potentially reducing efficacy for sedation or anxiety.

Key Considerations

Controlled substance

Lorazepam is a Schedule Schedule IV controlled substance under federal law. Prescriptions are regulated, refills may be restricted, and the medication has recognized potential for misuse or dependence. Use exactly as prescribed.

Known drug interactions

Lorazepam has documented interactions with other medications, supplements, and certain foods. Review the Drug Interactions section below and tell your healthcare provider about every medication you take, including over-the-counter products. Jump to section →

Multiple forms available

Lorazepam comes in more than one form (Oral tablet (0.5 mg, 1 mg, 2 mg), Oral concentrate solution (2 mg/mL), IV / IM injection (2 mg/mL, 4 mg/mL), Sublingual tablet (1 mg, 2 mg)). The right form for you depends on your condition, ease of use, and your provider's recommendation.

Additional Information

Lorazepam (Ativan) is a benzodiazepine used for anxiety, insomnia, status epilepticus, alcohol withdrawal, procedural sedation, and as an antiemetic in chemotherapy. Its pharmacokinetics make it the benzodiazepine of choice in several specific situations where others are less suitable.

Mechanism of Action

Lorazepam binds an allosteric site on the GABA-A receptor, increasing the frequency with which the chloride channel opens in response to GABA. Potentiating the principal inhibitory neurotransmitter produces anxiolysis, sedation, muscle relaxation, anterograde amnesia, and anticonvulsant activity.

Because it enhances GABA rather than acting directly on the channel, it cannot open it without GABA present — which is why benzodiazepines alone are comparatively difficult to overdose on fatally, and why combining them with opioids or alcohol removes that safety margin entirely.

Two pharmacokinetic features define lorazepam's place. It is conjugated directly by glucuronidation without requiring oxidative CYP metabolism, and it has no active metabolites. Most other benzodiazepines — diazepam and alprazolam among them — depend on hepatic oxidation and, in diazepam's case, generate long-lived active metabolites that accumulate.

That difference makes lorazepam the preferred benzodiazepine in liver disease and in older adults, where oxidative capacity declines and accumulation causes prolonged sedation and confusion. Glucuronidation is comparatively preserved in both groups.

Its intermediate half-life produces less inter-dose rebound than alprazolam while remaining shorter-acting than clonazepam. It is also reliably absorbed intramuscularly, unlike diazepam, which matters when intravenous access is unavailable in a seizing patient.

Clinical Use

In status epilepticus, intravenous lorazepam is a first-line agent, with a longer duration of anticonvulsant effect than diazepam because it redistributes out of the brain more slowly.

In alcohol withdrawal it is widely used, particularly in patients with liver disease where its metabolism is an advantage, and symptom-triggered dosing produces better outcomes than fixed schedules.

For anxiety, benzodiazepines have legitimate short-term uses — acute crisis, bridging the first weeks of an SSRI, procedural anxiety — but they are not first-line for chronic anxiety disorders. SSRIs and SNRIs such as sertraline and escitalopram, together with cognitive behavioural therapy, are, and CBT produces durable benefit that outlasts treatment in a way no medication does.

Tolerance develops to the anxiolytic effect with sustained use, so long-term benzodiazepine treatment often means taking a drug that no longer treats the condition while continuing to produce dependence. Where ongoing treatment is genuinely needed, the plan should be explicit from the outset. The St. Pete mental health guide covers alternatives, and our psychiatric team manages anxiety treatment.

Dependence and Withdrawal

Physical dependence develops with regular use over weeks and is a predictable pharmacologic consequence rather than a sign of addiction. It means abrupt cessation causes withdrawal, and benzodiazepine withdrawal is genuinely dangerous — unlike opioid withdrawal it can produce seizures and delirium and can be fatal.

Tapering must be gradual, over months rather than weeks after prolonged use. A patient taking lorazepam daily for years cannot simply be told to stop, and being told so is a common reason people obtain it elsewhere.

The FDA added a boxed warning in 2020 covering abuse, misuse, addiction, dependence, and withdrawal across the class, alongside the existing warning about combining benzodiazepines with opioids — a combination that substantially increases respiratory depression and overdose death. The FDA benzodiazepine safety communication sets this out.

Monitoring and Follow-Up

No laboratory monitoring is required. What must be monitored is the pattern of use: dose, frequency, whether it is escalating, whether early refills are requested, and whether the original indication still applies.

Prescription drug monitoring program checks are appropriate given the controlled-substance status. Falls, cognitive complaints, and daytime sedation should be assessed at each review, particularly in older patients.

Anterograde amnesia is a genuine effect and is exploited deliberately in procedural sedation, but it also means patients may not recall conversations or instructions given while taking it — worth knowing when important information is being conveyed.

The key review question is whether there is a plan. A patient with a documented taper plan and concurrent SSRI or therapy is in a different position from one refilled indefinitely with neither. The MedlinePlus lorazepam entry covers prescribing detail.

Special Populations

In older adults, benzodiazepines appear on lists of medications to avoid. They increase falls, fractures, motor vehicle accidents, and confusion, and are associated with cognitive impairment. Lorazepam is the least problematic of the class in this group because of its metabolism, which makes it the usual choice when one is genuinely required — but that is a relative rather than an absolute reassurance. The benzodiazepine deprescribing article covers tapering safely, which is often more valuable than any new prescription.

In hepatic impairment, lorazepam is preferred over oxidatively metabolised benzodiazepines. In pregnancy they are generally avoided, with neonatal withdrawal a concern with third-trimester use. They pass into breast milk. Lorazepam is contraindicated in narrow-angle glaucoma and warrants caution in significant respiratory disease and sleep apnea. A history of substance use disorder markedly raises the risk of problematic use.

Driving deserves an explicit word. Benzodiazepines impair reaction time and judgement measurably, the effect persists longer than the subjective sense of sedation, and it is additive with alcohol. Patients should not drive until they know how a dose affects them, and should not drive at all after a dose taken for acute anxiety.

When to Contact Your Doctor

Seek emergency care for extreme sleepiness, confusion, slowed or difficult breathing, or unresponsiveness — particularly if opioids, alcohol, or other sedatives are also involved.

Never stop lorazepam abruptly after regular use. Report withdrawal symptoms during a taper — anxiety, insomnia, tremor, sweating, sensory disturbance — so it can be slowed, and seek urgent care for seizure or severe confusion.

Report falls, memory problems, or daytime sedation. If the dose no longer lasts, or you are taking more than prescribed, raise it directly; that is a treatable situation rather than a reason for a difficult conversation.

To discuss anxiety treatment, plan a safe taper, or review whether a benzodiazepine is still appropriate, contact us or schedule a visit.

Frequently Asked Questions

Oral lorazepam is absorbed within 20 to 30 minutes, with peak effect in about 2 hours. Sublingual and IM routes work somewhat faster, and IV produces effects within minutes. Duration of clinical effect is typically 6 to 8 hours, which is why anxiety dosing is usually divided across the day.
Yes. Physical dependence can develop within 2 to 4 weeks of regular daily use, even at therapeutic doses, and tolerance to anti-anxiety effects often develops over months. Stopping abruptly after prolonged use can trigger withdrawal symptoms — anxiety, insomnia, tremor, and rarely seizures. Any taper should be gradual and physician-supervised.
The American Geriatrics Society Beers Criteria flag benzodiazepines as potentially inappropriate in adults 65 and older because of substantially increased risks of falls, hip fracture, motor vehicle accidents, cognitive impairment, and delirium. Older patients clear lorazepam more slowly, magnifying side effects. Non-benzodiazepine options should be considered first.
No. Combining alcohol with lorazepam significantly amplifies sedation, impairs coordination and judgment, and can dangerously suppress breathing. Even small amounts of alcohol can produce a much larger effect than expected. Avoid alcohol entirely while on this medication.
If you remember within an hour or two of the missed dose, take it as soon as possible. If it is close to the next scheduled dose, skip the missed one and resume your regular schedule — do not double up. If you have been taking lorazepam regularly and miss multiple doses, contact your prescriber to discuss safe restart and any withdrawal-mitigation steps.

Medical Disclaimer: This information is for educational purposes only and should not be considered medical advice. Always consult with your healthcare provider before starting, stopping, or changing any medication. Your doctor can provide personalized recommendations based on your specific health condition and medical history.