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Bedside Snapshot
- Core dose: Seizures: 0.15–0.2 mg/kg IV (max 10 mg) at ≤5 mg/min, may repeat once; agitation: 2–10 mg IV titrated to effect; alcohol withdrawal: 10–20 mg IV/PO every 5–15 min until calm; rectal 0.5 mg/kg (max 20 mg) if no IV
- Onset/duration: IV onset 1–3 min, rectal 5–10 min; anticonvulsant effect ~15–30 min after single IV bolus due to redistribution; elimination half-life 20–50 h (active metabolites 30–100+ h)
- Key danger: Respiratory depression/apnea (especially with opioids or alcohol); hypotension; accumulation with repeated dosing (long-acting metabolites); paradoxical agitation (rare); avoid IM (erratic absorption)
- Special: Benzodiazepine (GABA_A positive allosteric modulator); high lipophilicity → rapid CNS penetration but redistributes quickly; can use rectal route if no IV; flumazenil is reversal agent (use cautiously in seizure patients); propylene glycol vehicle
Brand & Generic Names
- Generic Name: diazepam (oral/IV/rectal)
- Brand Names: Valium (PO/IV), Diastat/Diastat AcuDial (rectal gel)
Medication Class
Benzodiazepine; anticonvulsant, anxiolytic, sedative-hypnotic, muscle relaxant
Pharmacology
Mechanism of Action:
- Positive allosteric modulator of GABA_A receptors at the benzodiazepine site
- Rapid CNS penetration due to high lipophilicity
- Anticonvulsant effect is fast but redistributes from brain to peripheral tissues within ~15–30 min after IV dose
Pharmacokinetics (clinically relevant):
- Onset: IV 1–3 min; PR ~5–10 min; IM is erratic/slow—avoid for emergencies
- Duration (anticonvulsant): ~15–30 min after single IV bolus due to redistribution (despite long elimination half-life)
- Half-life: diazepam ~20–50 h; active metabolite desmethyldiazepam (nordiazepam) 30–100+ h → accumulation with repeated dosing, especially elderly/hepatic impairment
- Metabolism: hepatic (CYP2C19, CYP3A4) to desmethyldiazepam, temazepam, oxazepam
- Protein binding: highly protein bound (~98–99%)
- Elimination: hepatic/biliary; renal excretion of metabolites. Not dialyzable in overdose to any meaningful degree
Indications
- Status epilepticus/acute repetitive seizures
- Sedation and agitation control in hyperadrenergic states (e.g., stimulant toxicity), serotonin syndrome (adjunct), and tetanus
- Alcohol withdrawal/DTs (symptom-triggered or loading strategies)
- Muscle spasm (e.g., severe back spasm) and spasticity (adjunct)
- Chemical agent/nerve agent seizure control (CANA auto-injector; military/CBRN protocols)
Conditions Treated
- Status epilepticus
- Acute repetitive seizures
- Stimulant toxicity (agitation control)
- Serotonin syndrome
- Alcohol withdrawal syndrome / Delirium tremens
- Severe muscle spasm and spasticity
- Tetanus
- Nerve agent exposure (seizure control)
Dosing & Administration
Available Forms:
- Injection: 5 mg/mL (2 mL = 10 mg; 10 mL = 50 mg)
- Rectal gel (Diastat): weight-based prefilled doses (2.5–20 mg)
- Oral tablets: 2 mg, 5 mg, 10 mg
Adult Dosing:
| Indication | Dose | Notes |
|---|---|---|
| Status epilepticus/active seizure | 0.15–0.2 mg/kg IV (max 10 mg) at ≤5 mg/min | May repeat once after 5–10 min. If IV unavailable, PR 0.5 mg/kg (max 20 mg) |
| Acute agitation/hyperadrenergic toxicity | 2–10 mg IV | Repeat titrated to effect and BP/respiratory status |
| Alcohol withdrawal | 10–20 mg IV/PO every 5–15 min until calm but arousable | Then scheduled/PRN per CIWA or ICU protocol; high cumulative doses may be required |
| Muscle spasm | 2–10 mg PO/IV every 6–8 h as needed | Use lowest effective dose |
Pediatric Dosing:
- Seizure: IV/IO 0.2 mg/kg (max 10 mg), may repeat once; PR 0.5 mg/kg (max 20 mg)
- Rectal gel (Diastat) rescue: 0.2–0.5 mg/kg with rounding to prefilled strengths; one repeat dose after 4–12 h per labeling/protocol
Administration:
- Administer undiluted IV push into a large vein; avoid mixing with other drugs/fluids
- Injection is nonaqueous and incompatible with many solutions—administer via slow IV push into a running line
- Do not mix with other medications
Contraindications
Contraindications:
- Acute narrow-angle glaucoma
- Severe respiratory insufficiency without ventilatory support
- Hypersensitivity to benzodiazepines
Boxed Warnings:
- Concomitant use with opioids may cause profound sedation, respiratory depression, coma, and death
- Risk of abuse, misuse, and addiction
- Physical dependence and withdrawal reactions
Precautions:
- Use caution in hepatic impairment (risk of oversedation/encephalopathy)
- Elderly (falls, delirium)
- Sleep apnea
- Myasthenia gravis
- Substance use disorders
- Pregnancy (neonatal CNS/respiratory depression if used near delivery)
- Avoid routine IM route (erratic absorption, tissue irritation)
Opioid Combination: Concomitant use with opioids increases risk of profound sedation, respiratory depression, coma, and death.
Adverse Effects
Dose-related CNS Depression:
- Somnolence
- Ataxia
- Confusion
- Anterograde amnesia
- Paradoxical agitation (rare)
Cardiorespiratory:
- Respiratory depression, especially with other CNS depressants or rapid IV push
- Hypotension
Local:
- Pain, thrombophlebitis
- Propylene glycol–containing injection can cause hypotension/metabolic acidosis with high cumulative dosing
Drug Interactions
- Opioids, alcohol, antihistamines, antipsychotics, other sedatives: Additive CNS/respiratory depression
- CYP3A4/CYP2C19 inhibitors (fluconazole, fluoxetine, omeprazole, cimetidine, clarithromycin): May increase diazepam levels
- CYP inducers (rifampin, carbamazepine): May decrease effect
- Clozapine: Avoid during acute titration (respiratory/circulatory collapse reported); monitor closely if necessary
Clinical Pearls
Status Epilepticus: Follow diazepam with a longer-acting antiepileptic (e.g., levetiracetam, fosphenytoin, valproate) because anticonvulsant effect of a single bolus is short (redistribution).
Route Selection: Prefer IV/IO or rectal over IM for emergencies. If only IM route is available, midazolam is preferred.
Alcohol Withdrawal: Titrate using symptom-triggered protocols when possible; diazepam's long half-life smooths rebound between doses.
Flumazenil Caution: Avoid flumazenil in undifferentiated overdose or chronic benzodiazepine users—can precipitate refractory seizures; reserve for select iatrogenic cases with airway secured.
Stimulant Toxicity/Serotonin Syndrome: Benzodiazepines are first-line to control agitation and autonomic hyperactivity; treat hyperthermia with external cooling (avoid antipsychotics in severe stimulant toxicity).
Administration Compatibility: Injection is nonaqueous and incompatible with many solutions—administer undiluted via slow IV push into a running line; do not mix with other medications.
References
- 1. Papadopoulos, J. (2008). Pocket guide to critical care pharmacotherapy. Humana Press.
- 2. Medscape. (n.d.). Diazepam (Valium, Diastat) – drug monograph & dosing. Retrieved 2025-11-12, from https://reference.medscape.com
- 3. Medscape. (n.d.). Status epilepticus: Treatment & management. Retrieved 2025-11-12, from https://emedicine.medscape.com
- 4. Medscape. (n.d.). Alcohol withdrawal syndrome: Treatment. Retrieved 2025-11-12, from https://emedicine.medscape.com
- 5. DrugBank Online. (n.d.). Diazepam (DB00829). Retrieved 2025-11-12, from https://go.drugbank.com/drugs/DB00829