Comprehensive Guide to Ketamine: Uses, Dosage, Side Effects, and More
What is Ketamine?
Overview of Ketamine
Generic Name: Ketamine
Brand Name: Ketalar, Spravato (esketamine nasal spray), generics
Drug Group: Dissociative anesthetic (NMDA antagonist)
Commonly Used For
- Induce and maintain general anesthesia.
- Manage acute pain in emergencies.
- Treat treatment-resistant depression (TRD).
Key Characteristics
Form: Injectable solution (10 mg/mL, 50 mg/mL, 100 mg/mL), intranasal spray (esketamine 28 mg), or oral (off-label) (detailed in Dosage section).
Mechanism: Blocks NMDA receptors, producing dissociative anesthesia and rapid antidepressant effects.
Approval: FDA-approved (1970 for Ketalar); esketamine approved (2019 for TRD) and EMA-approved for specific indications.

Indications and Uses of Ketamine
Ketamine is indicated for a range of anesthetic, analgesic, and psychiatric conditions, leveraging its unique pharmacological profile:
General Anesthesia: Induces and maintains anesthesia in surgical procedures, particularly in resource-limited settings, per anesthesiology guidelines, supported by trials showing stable hemodynamics.
Acute Pain Management: Treats severe pain in trauma or burn patients, reducing opioid reliance, recommended in emergency medicine protocols with evidence of rapid onset.
Treatment-Resistant Depression (TRD): Alleviates depressive symptoms in TRD patients, with esketamine showing response rates of 50–70% within 24 hours, per psychiatry studies.
Post-Traumatic Stress Disorder (PTSD): Investigated off-label to reduce flashbacks and hyperarousal, with psychotherapy-enhanced outcomes, supported by trauma research.
Chronic Pain Syndromes: Managed off-label for neuropathic pain or fibromyalgia, improving quality of life, with pain management data.
Status Epilepticus: Explored off-label as a second-line treatment, controlling seizures, per neurology studies.
Sedation in Pediatrics: Used off-label for procedural sedation in children, with pediatric anesthesiology evidence.
Suicidal Ideation: Initiated off-label to reduce acute suicidal thoughts, with psychiatric emergency research.
Alcohol Withdrawal: Investigated off-label to manage severe agitation, with addiction medicine data.
Opioid-Sparing Anesthesia: Applied off-label to minimize intraoperative opioid use, with surgical anesthesiology studies.
Dosage of Ketamine
Dosage for Adults
General Anesthesia:
IV: 1–2 mg/kg for induction, followed by 0.5–1 mg/kg/hour for maintenance.
IM: 6.5–13 mg/kg for induction, with effects lasting 10–20 minutes.
Acute Pain Management:
IV: 0.1–0.5 mg/kg over 10–15 minutes, repeated every 1–2 hours as needed.
IM: 0.5–1 mg/kg every 4–6 hours.
Treatment-Resistant Depression (TRD):
Intranasal (Esketamine): 56 mg or 84 mg twice weekly for 4 weeks, then tapered, under psychiatric supervision.
Dosage for Children (≥3 months)
Procedural Sedation (Off-Label):
IV: 0.5–2 mg/kg, with maintenance doses of 0.25–0.5 mg/kg as needed.
IM: 4–6 mg/kg, adjusted based on age and weight, under pediatric oversight.
Dosage for Pregnant Women
Pregnancy Category B: Use only if benefits outweigh risks; consult an obstetrician and anesthesiologist, with fetal monitoring.
Dosage Adjustments
Renal Impairment: No adjustment needed for mild cases; reduce dose in severe impairment (CrCl <30 mL/min) and monitor.
Hepatic Impairment:
Mild to moderate (Child-Pugh A or B): Use cautiously with reduced dose; severe (Child-Pugh C): Avoid due to prolonged clearance.
Concomitant Medications: Adjust if combined with CNS depressants (e.g., benzodiazepines), increasing sedation risk; monitor respiratory status.
Elderly: Start with lower doses (e.g., 0.5 mg/kg IV); monitor for cardiovascular effects.
Psychiatric Use: Limit to supervised settings with follow-up to assess psychological impact.
Additional Considerations
- Administer this active ingredient in a controlled environment with resuscitation equipment available.
- Use intranasal esketamine with a 2-hour observation period post-dose for TRD.
- Avoid rapid IV bolus to minimize hemodynamic changes.
How to Use Ketamine
Administration:
IV: Infuse slowly over 1–2 minutes into a secure line, with continuous monitoring.
IM: Inject into a large muscle (e.g., deltoid or gluteal) for rapid effect.
Intranasal: Administer esketamine spray into alternating nostrils, following device instructions.
Timing: Administer as a single dose or continuous infusion based on procedure or condition, with TRD doses spaced per protocol.
Monitoring: Watch for respiratory depression, hypertension, or hallucinations; use pulse oximetry and ECG.
Additional Tips:
- Store at 20–25°C (68–77°F), protecting from light; refrigerate esketamine spray.
- Keep out of reach of children; restrict access due to abuse potential.
- Provide a quiet recovery environment to minimize emergence reactions.
- Educate patients on potential dissociative effects and need for a caregiver post-use.
- Schedule regular follow-ups for psychiatric patients to assess mood and side effects.
Contraindications for Ketamine
Hypersensitivity: Patients with a known allergy to Ketamine or its components.
Severe Hypertension or Heart Failure: Contraindicated due to cardiovascular stimulation risk.
Psychosis: Avoid in active schizophrenia or bipolar mania due to exacerbation risk.
Severe Liver Disease: Contraindicated in Child-Pugh Class C due to impaired metabolism.
Elevated Intracranial Pressure: Avoid in head injury or brain tumors due to increased pressure risk.
Severe Respiratory Depression: Contraindicated in patients with compromised airways.
Concurrent Use with MAOIs: Avoid within 14 days due to hypertensive crisis risk.
Warnings & Precautions for Ketamine
General Warnings
Respiratory Depression: Risk with high doses or rapid administration; monitor with capnography.
Emergence Reactions: Risk of hallucinations or agitation post-anesthesia; use benzodiazepines if needed.
Cardiovascular Stimulation: Risk of hypertension or tachycardia; assess cardiac status.
Increased Intraocular Pressure: Risk in glaucoma patients; avoid unless benefits outweigh risks.
Dependence Potential: Risk of psychological dependence with repeated use; limit to supervised settings.
Additional Warnings
Liver Injury: Rare elevation of liver enzymes; monitor hepatic function in chronic use.
Cognitive Impairment: Risk of memory issues with repeated doses; assess neuropsychiatric status.
Anaphylaxis: Rare severe allergic reactions; discontinue if swelling occurs.
Renal Impairment: Risk of accumulation; monitor creatinine in severe cases.
Hypersensitivity Reactions: Rare rash or bronchospasm; stop if severe.
Use in Specific Populations
Pregnancy: Category B; use with caution, monitoring fetal outcomes.
Breastfeeding: Use caution; monitor infant for sedation.
Elderly: Higher risk of cardiovascular effects; start with reduced doses.
Children: Safe for sedation with pediatric oversight.
Renal/Hepatic Impairment: Adjust or avoid based on severity.
Additional Precautions
- Inform your doctor about heart conditions, psychiatric history, or liver disease before starting this medication.
- Avoid alcohol or sedatives during therapy to reduce respiratory risk.
- Use protective measures (e.g., side rails) during recovery to prevent injury from agitation.
Overdose and Management of Ketamine
Overdose Symptoms
- Drowsiness, nystagmus, or hypertension.
- Severe cases: Respiratory arrest, coma, or cardiovascular collapse.
- Hallucinations, vomiting, or seizures as early signs.
- Profound sedation or death with extremely high doses.
Immediate Actions
Contact the Medical Team: Seek immediate medical help if overdose is suspected.
Supportive Care: Secure airway, provide oxygen, and support ventilation if needed.
Specific Treatment: No specific antidote; use benzodiazepines for agitation or physostigmine for severe hallucinations under specialist guidance.
Monitor: Check vital signs, oxygen saturation, and mental status for 24–48 hours.
Patient Education: Advise against self-administering and to store securely.
Additional Notes
- Overdose risk is high with recreational use; store in a locked location.
- Report persistent symptoms (e.g., confusion, irregular breathing) promptly.
Side Effects of Ketamine
Common Side Effects
- Hallucinations (10–20%, managed with benzodiazepines)
- Nausea (5–15%, relieved with antiemetics)
- Dizziness (5–10%, decreases with rest)
- Hypertension (3–8%, monitored with BP checks)
- Vomiting (2–6%, controlled with hydration)
These effects may subside with adaptation or dose adjustment.
Serious Side Effects
Seek immediate medical attention for:
- Respiratory: Apnea or severe depression.
- Cardiovascular: Myocardial infarction or arrhythmias.
- Neurological: Prolonged psychosis or seizures.
- Hepatic: Liver failure (rare with chronic use).
- Allergic: Anaphylaxis or rash (rare).
Additional Notes
Regular monitoring with ECG and respiratory support is advised during administration.
Patients with a history of substance abuse should be closely watched for dependence.
Report any unusual symptoms (e.g., chest pain, persistent hallucinations) immediately to a healthcare provider.
Long-term use requires liver function tests and psychiatric evaluations to assess cognitive impact.
Drug Interactions with Ketamine
This active ingredient may interact with:
- CNS Depressants: Increases sedation (e.g., opioids, benzodiazepines); monitor respiration.
- MAOIs: Enhances hypertensive risk; avoid within 14 days.
- Thyroid Hormones: Amplifies cardiovascular effects; use cautiously.
- Anticholinergics: Potentiates tachycardia; adjust dose.
- Antidepressants: May alter mood effects; monitor closely.
Action: Provide your healthcare provider with a complete list of medications.
Patient Education or Lifestyle
Medication Adherence: Use this anesthetic as prescribed for anesthesia or depression, following medical guidance.
Monitoring: Report hallucinations, breathing issues, or mood changes immediately.
Lifestyle: Avoid driving for 24 hours post-dose; limit alcohol.
Diet: No specific restrictions; take with water if oral.
Emergency Awareness: Know signs of overdose or respiratory distress; seek care if present.
Follow-Up: Schedule regular check-ups to monitor mental health and liver function.
Pharmacokinetics of Ketamine
Absorption: IV (immediate), IM (peak 5–15 minutes), intranasal (peak 20–40 minutes); bioavailability ~20–50% (oral).
Distribution: Volume of distribution ~3 L/kg; 20–50% protein-bound.
Metabolism: Hepatic via CYP3A4 and CYP2B6 to norketamine (active metabolite).
Excretion: Primarily renal (as metabolites); half-life 2–3 hours.
Half-Life: 2–3 hours, with norketamine extending effects.
Pharmacodynamics of Ketamine
This drug exerts its effects by:
Blocking NMDA receptors, producing dissociative anesthesia and analgesia.
Increasing glutamate release, contributing to rapid antidepressant effects.
Exhibiting dose-dependent risks of psychosis and respiratory depression.
Storage of Ketamine
Temperature: Store at 20–25°C (68–77°F); protect from light.
Protection: Keep in original container, away from heat and humidity.
Safety: Store in a secure, locked location out of reach of children due to abuse risk.
Disposal: Dispose of unused vials or sprays per local regulations or consult a pharmacist.
Frequently Asked Questions (FAQs)
Q: What does Ketamine treat?
A: This medication treats anesthesia and depression.
Q: Can this active ingredient cause hallucinations?
A: Yes, hallucinations are common; report if severe.
Q: Is Ketamine safe for children?
A: Yes, for sedation with supervision.
Q: How is this drug taken?
A: Via IV, IM, or intranasal, as directed.
Q: How long is Ketamine treatment?
A: Varies by use, from single dose to weeks for depression.
Q: Can I use Ketamine if pregnant?
A: Yes, with caution; consult a doctor.
Regulatory Information
This medication is approved by:
U.S. Food and Drug Administration (FDA): Approved in 1970 (Ketalar) for anesthesia; 2019 (Spravato) for TRD.
European Medicines Agency (EMA): Approved for anesthesia and esketamine for TRD.
Other Agencies: Approved globally for anesthesia; consult local guidelines.
References
- U.S. Food and Drug Administration (FDA). (2023). Ketalar (Ketamine) Prescribing Information.
- Official FDA documentation detailing the drug’s approved uses, dosage, and safety.
- European Medicines Agency (EMA). (2023). Ketamine Summary of Product Characteristics.
- EMA’s comprehensive information on the medication’s indications and precautions in Europe.
- National Institutes of Health (NIH). (2023). Ketamine: MedlinePlus Drug Information.
- NIH resource providing detailed information on the drug’s uses, side effects, and precautions.
- World Health Organization (WHO). (2023). WHO Model List of Essential Medicines: Ketamine.
- WHO’s inclusion of Ketamine for anesthesia.
- Journal of Clinical Psychiatry. (2022). Ketamine in Depression.
- Peer-reviewed article on Ketamine efficacy (note: access may require a subscription).