Ketamine (Anaesthesia/Sedation)
Brand names: Ketalar
Ketamine is a dissociative anaesthetic used for anaesthesia and procedural sedation, and at lower doses for analgesia; it is valued where airway reflexes and blood pressure need to be preserved (e.g. trauma, asthma).
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
US labelling (FDA)
Reference — US labelling, may differ from UKSee Full Prescribing Information for important dosage and administration instructions. ( 2 ) Induction of anesthesia: -- Intravenous route : Initially, 1 to 4.5 mg/kg administered slowly (over a period of 60 seconds). Alternatively, administer a dose of 1 to 2 mg/kg at a rate of 0.5 mg/kg/min. ( 2.2 ) -- Intramuscular route : Initially, 6.5 to 13 mg/kg. ( 2.2 ) Maintenance of anesthesia: Increments of one-half to the full induction dose may be repeated as needed ( 2.2 ). Adjust the dose according to the patient's anesthetic needs and whether an additional anesthetic agent is employed. ( 2.2 ) Supplement to other anesthetic agents : The regimen of a reduced dose of KETALAR supplemented with …
Source: US FDA prescribing information (openFDA / DailyMed), label dated 2026-03-27. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.
Clinical monograph
How it works
It is mainly an NMDA-receptor antagonist, producing dissociative anaesthesia with relative preservation of airway tone and respiration, bronchodilation and sympathetic stimulation.
Prescribing in practice
- It tends to maintain or raise blood pressure and causes bronchodilation, useful in shock or severe asthma.
- Emergence phenomena (vivid dreams, hallucinations, agitation) occur — a quiet recovery and a benzodiazepine can help; it increases secretions.
- It is a controlled drug with recognised misuse potential.
Monitoring
Monitor conscious level, airway, oxygenation, heart rate and blood pressure; observe during emergence.
Counselling the patient
- You may feel detached or have vivid dreams as it wears off.
- Do not drive or make important decisions for the rest of the day.
Evidence & guidelines
Used for anaesthesia/procedural sedation and analgesia, particularly where haemodynamic stability or bronchodilation is wanted.
Reference: Miller's Anaesthesia; WHO Model List of Essential Medicines; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Modified Mallampati Classification · Airway Assessment
- Richmond Agitation-Sedation Scale (RASS) · Sedation Assessment
- Confusion Assessment Method for ICU (CAM-ICU) · Delirium Assessment
- ASA Physical Status Classification · Pre-operative Risk
- Aldrete Score for Post-Anaesthesia Discharge · Post-operative
- Ramsay Sedation Scale · Sedation
- Paracetamol overdose · TOXBASE/NPIS; MHRA DSU 2012/2024; SNAP regimen (Lancet 2014)
- TCA overdose · TOXBASE/NPIS; AACT/EAPCCT position statements; Resuscitation Council UK ALS
- Opioid overdose · TOXBASE/NPIS; Resuscitation Council UK
- Anticholinergic toxidrome · TOXBASE/NPIS; AACT/EAPCCT
- Benzodiazepine overdose · TOXBASE/NPIS; AACT/EAPCCT
- β-blocker overdose · TOXBASE/NPIS; AACT/EAPCCT; ESC