Product image of Ketolar (Ketamine Hydrochloride) supplied by GNH India

Ketolar

Active Ingredient:
Ketamine Hydrochloride
Origin:
EU

Ketolar (Ketamine Hydrochloride)

Ketamine, the active ingredient in Ketolar, is a NMDA receptor antagonist presented as a sterile injectable solution for intramuscular and intravenous use. It is employed in anesthesia, analgesia and sedation, and is also investigated off‑label for treatment‑resistant depression in appropriate clinical settings.

GNH India supplies Ketolar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Pfizer S.L.

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Indications & Clinical Uses

Ketolar acts on the central nervous system by blocking NMDA receptors, providing anesthetic and analgesic effects.

  • Anesthesia: induces a reversible loss of consciousness and analgesia for surgical procedures.
  • Analgesia: provides profound pain relief during and after surgery or in acute pain management.
  • Sedation: facilitates deep sedation for diagnostic or therapeutic interventions.
  • Treatment‑resistant depression (off‑label): may produce rapid antidepressant effects under specialist supervision.

How It Works

  • Ketamine is a non‑competitive antagonist of the N‑methyl‑D‑aspartate (NMDA) receptor, binding to the receptor-associated ion channel and reducing calcium influx. This inhibition disrupts excitatory neurotransmission, leading to decreased neuronal firing and modulation of downstream pathways such as opioid receptors and monoaminergic systems, which together produce anesthetic, analgesic, and dissociative effects.

Side Effects

Ketolar may cause a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Hypertension: transient increase in blood pressure during administration.
  • Tachycardia: elevated heart rate observed in some patients.
  • Nausea: mild to moderate feeling of queasiness.
  • Vomiting: occasional emesis following dosing.
  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Visual disturbances: blurred vision or altered perception.

Serious or Rare Side Effects

  • Respiratory depression: reduced breathing effort requiring support.
  • Emergence reactions: vivid dreams, agitation, or hallucinations during recovery.
  • Cardiac arrhythmias: irregular heart rhythms in susceptible individuals.
  • Elevated intracranial pressure: worsening of pre‑existing conditions.
  • Hepatotoxicity: rare liver enzyme elevations.
  • Allergic reactions: rash, itching, or anaphylaxis in extreme cases.

Precautions & Warnings

Ketolar should be administered by qualified healthcare professionals with appropriate monitoring.

  • Cardiovascular assessment: evaluate blood pressure and heart rate before use.
  • Respiratory monitoring: ensure adequate ventilation and oxygenation during and after administration.
  • Psychiatric history: consider risk of emergence reactions in patients with psychosis.
  • Substance abuse: use caution in individuals with a history of ketamine misuse.
  • Drug interactions: review concomitant medications for potential additive CNS effects.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Ketolar can interact with other agents that affect the central nervous system or cardiovascular function.

Major Interactions (Avoid)

  • Central depressants (e.g., benzodiazepines, opioids): may cause profound respiratory depression.
  • Sympathomimetic agents (e.g., epinephrine): can exacerbate hypertension and tachycardia.

Moderate Interactions (Monitor Closely)

  • Monoamine oxidase inhibitors: risk of hypertensive crisis.
  • Anticholinergic drugs: may increase intra‑ocular pressure.
  • CYP450 substrates (e.g., CYP2B6, CYP3A4): ketamine metabolism may be altered, affecting drug levels.

Frequently Asked Questions

Ketolar contains ketamine hydrochloride and is used primarily as an anesthetic agent to induce loss of consciousness, provide analgesia during surgery, and facilitate deep sedation for diagnostic or therapeutic procedures. It may also be employed off‑label for treatment‑resistant depression under specialist supervision.

Ketamine blocks the NMDA receptor, a type of glutamate receptor in the brain, preventing calcium influx and reducing excitatory neurotransmission. This action leads to dissociation, analgesia, and anesthesia, while also influencing opioid and monoaminergic pathways that contribute to its pain‑relieving and mood‑modulating effects.

The dosage of Ketolar is determined by the prescribing clinician based on the patient’s age, weight, medical condition, and the intended procedure. Healthcare professionals calculate the appropriate amount and route of administration to achieve the desired anesthetic or analgesic effect.

The safety of ketamine during pregnancy or lactation has not been definitively established. It is generally classified as a drug with unknown pregnancy category, and clinicians weigh potential benefits against risks before prescribing to pregnant or nursing individuals.

To request Ketolar, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and any required import documentation.

Ketolar (ketamine) differs from many inhalational or opioid‑based anesthetics by providing both dissociative anesthesia and analgesia without significant respiratory depression. Its rapid onset and short duration make it useful for short procedures, whereas agents like propofol may cause deeper sedation but require airway management.

Ketolar should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Maintaining the cold‑chain ensures the stability and sterility of the injectable solution.

Ketolar is supplied as a sterile solution for intramuscular or intravenous injection. Administration is performed by qualified healthcare personnel, who monitor vital signs and adjust the dose as needed to achieve the desired anesthetic depth or analgesic effect.

Serious risks include respiratory depression, emergence reactions such as vivid dreams or hallucinations, cardiovascular effects like hypertension and tachycardia, and rare allergic reactions. Continuous monitoring during and after administration helps detect and manage these events promptly.

Ketolar is contraindicated in patients with known hypersensitivity to ketamine or its excipients, those with uncontrolled hypertension, severe cardiovascular disease, or a history of psychosis that may be exacerbated by dissociative effects. Clinical judgment is essential to determine suitability.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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