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Oxazepam

Short-acting benzodiazepine (no active metabolites) · Anxiolytic

START
10–15 mg PO 3 times daily (elderly: 10 mg BID–TID)
TYPICAL MAX
120 mg/day (alcohol withdrawal); 60 mg/day anxiety
STOP IF
Dependence signs, falls, or significant sedation
WATCH
Falls, cognition (elderly), respiratory status, taper plan
CDSCO approvedATC N05BA04
Dose laddermg/d
30start/day60anxiety max120withdrawal
Renal dose adjustmenteGFR mL/min/1.73m²
FULLNo dose adjustment at any eGFR90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
45minONSET2.5hPEAK10h5hDURATION
ONSET
45min · absorption
PEAK
2.5h · Tmax
10h ·
DURATION
5h · per dose
EXCRETION
Renal — glucuronide conjugate
route + CYP
INTERACTIONS
12 major
SEVERE in our sources
PREGNANCY
Avoid (cleft palate, neonatal withdrawal).
FDA category + note
Top interactionssee all 12
  • MethylnaltrexoneSevereTextbookG&G 14e
  • NalmefeneSevereTextbookG&G 14e
  • NaloxoneSevereTextbookG&G 14e
  • NaltrexoneSevereTextbookG&G 14e

Mechanism

Allosteric agonist at GABA-A receptor benzodiazepine site, potentiating chloride conductance; metabolised purely by glucuronidation (no oxidative metabolism), with no active metabolites — favoured in elderly and hepatic impairment.

Indications

Anxiety disorders (short-term)Anxiety associated with depression (short-term adjunct)Alcohol withdrawal (in elderly / hepatic impairment)

Dosing

Adult
10–30 mg PO 3–4 times daily; alcohol withdrawal up to 120 mg/day. Short-term use only.
Pediatric
Not generally recommended.
Renal adjustment
No specific adjustment.
Hepatic adjustment
Preferred benzodiazepine (no active metabolites); usual dose.
Geriatric
Preferred over long-acting BZDs; start 10 mg twice–thrice daily.
Max dose
120 mg/day (alcohol withdrawal); 60 mg/day chronic anxiety (short-term)

Pharmacokinetics

Onset
~30–60 min (oral)
Peak effect
~2–3 h
Duration
~4–6 h (per dose)
Half-life
~5–15 h (no active metabolites)
Bioavailability
Well absorbed orally
Protein binding
~87%
Metabolism
Hepatic glucuronidation only (Phase II)
Excretion
Renal (glucuronide)

Contraindications

  • Severe respiratory insufficiency / sleep apnoea
  • Acute angle-closure glaucoma
  • Myasthenia gravis
  • Pregnancy/breastfeeding
  • Hypersensitivity

Side effects

Common
DrowsinessDizzinessFatigueConfusion (elderly)
Serious
  • Dependence/withdrawal
  • Falls/fractures (elderly)
  • Respiratory depression (with opioids/alcohol)
  • Paradoxical agitation

Pregnancy & lactation

Pregnancy

Avoid (cleft palate, neonatal withdrawal).

Lactation

Avoid (low milk levels but cumulative effect).

Drug interactions

Methylnaltrexone
Severe
Textbook

Increased rates of accidental overdose and death.

Caution is advised, especially for patients with a history of drug abuse.

Source: G&G 14e

Nalmefene
Severe
Textbook

Increased rates of accidental overdose and death.

Caution is advised, especially for patients with a history of drug abuse.

Source: G&G 14e

Naloxone
Severe
Textbook

Increased rates of accidental overdose and death.

Caution is advised, especially for patients with a history of drug abuse.

Source: G&G 14e

Naltrexone
Severe
Textbook

Increased rates of accidental overdose and death.

Caution is advised, especially for patients with a history of drug abuse.

Source: G&G 14e

Other Cns Depressants
Severe
Textbook

Typically fatal if combined in overdose.

Use with extreme caution; avoid if possible.

Source: G&G 14e

Alfentanil
Severe
Database

Increased rates of accidental overdose and death.

Caution is advised, especially for patients with a history of drug abuse.

Source: DDInter

Benzhydrocodone
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Buprenorphine
Severe
Database

Increased rates of accidental overdose and death.

Caution is advised, especially for patients with a history of drug abuse.

Source: DDInter

Butorphanol
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Clozapine
Severe
Database

Drug interaction classified as: synergy.

Source: DDInter

Codeine
Severe
Database

Increased rates of accidental overdose and death.

Caution is advised, especially for patients with a history of drug abuse.

Source: DDInter

Dextropropoxyphene
Severe
Database

Clinical effect not specified

Source: DDInter

Related guidelines

Ask House about Oxazepam

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Katzung·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20