Product image of Ketalar (Ketamine) supplied by GNH India

Ketalar

Active Ingredient:
Ketamine
Origin:
EU

Ketalar (Ketamine)

Ketamine, the active ingredient in Ketalar, is an NMDA receptor antagonist presented as a sterile injectable solution for intramuscular and intravenous use. It produces dissociative anesthesia and analgesia, and is employed in surgical and procedural settings for patients requiring rapid induction of unconsciousness or pain control.

GNH India supplies Ketalar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide, including tertiary care centers, surgical suites and emergency departments, with adherence to global quality standards and ensuring reliable delivery across regulated markets.

Manufacturer / TM Owner

Pfizer Limited

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Indications & Clinical Uses

Ketalar is used in the anesthetic pathway to provide rapid dissociative anesthesia and analgesia.

  • Induction of anesthesia: enables quick loss of consciousness for surgical procedures.
  • Analgesia: provides pain relief during painful procedures or trauma care.
  • Sedation: facilitates moderate sedation for diagnostic or therapeutic interventions.

How It Works

  • Ketamine acts as a non‑competitive antagonist at the N‑methyl‑D‑aspartate (NMDA) receptor, binding to the phencyclidine site within the ion channel. By blocking calcium influx, it interrupts excitatory neurotransmission, producing dissociative anesthesia, analgesia, and cataleptic states. Additional actions at opioid receptors, monoaminergic pathways, and voltage‑gated calcium channels contribute to its analgesic and sympathomimetic effects.

Side Effects

Ketamine may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Hypertension: transient increase in blood pressure.
  • Tachycardia: elevated heart rate.
  • Nausea: feeling of sickness.
  • Vomiting: expulsion of stomach contents.
  • Dizziness: light‑headed sensation.
  • Visual disturbances: blurred or altered vision.

Serious or Rare Side Effects

  • Respiratory depression: reduced breathing effort.
  • Laryngospasm: sudden closure of the vocal cords.
  • Hallucinations: vivid perceptual disturbances.
  • Severe hypertension: dangerous rise in blood pressure.
  • Allergic reaction: rash, itching, swelling, or anaphylaxis.

Precautions & Warnings

When using Ketalar, clinicians should observe several safety measures to minimize risk.

  • Patient assessment: evaluate cardiovascular and respiratory status before administration.
  • Dose titration: adjust dose based on age, weight, and clinical response.
  • Monitoring: continuously observe blood pressure, heart rate, and oxygen saturation during and after dosing.
  • Contraindications: avoid use in patients with known hypersensitivity to ketamine or severe uncontrolled hypertension.
  • Drug interactions: review concomitant medications that may potentiate CNS depression or sympathomimetic effects.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Ketalar can interact with other agents, altering its safety profile or efficacy.

Major Interactions (Avoid)

  • Benzodiazepines: may blunt anesthetic effects and increase respiratory depression risk.
  • Opioids: synergistic CNS depression can lead to profound sedation.
  • MAO inhibitors: heightened risk of hypertensive crisis.

Moderate Interactions (Monitor Closely)

  • Sympathomimetic agents (e.g., epinephrine): may exacerbate hypertension and tachycardia.
  • Anticholinergic drugs: can increase intra‑ocular pressure and affect heart rate.
  • CNS stimulants (e.g., amphetamines): may counteract sedative properties.

Frequently Asked Questions

Ketalar is a brand name for ketamine used primarily as a general anesthetic. It provides rapid induction of anesthesia, analgesia during painful procedures, and moderate sedation for diagnostic or therapeutic interventions in hospital settings.

Ketamine works by blocking the NMDA receptor, a key component of excitatory neurotransmission in the central nervous system. This antagonism prevents calcium influx, leading to dissociative anesthesia, analgesia, and a range of psychomimetic effects.

The dose of Ketalar is determined by the prescribing clinician based on the patient’s age, weight, clinical condition, and the intended procedure. Specific dosing regimens are not disclosed publicly and should follow the prescriber’s order.

Safety data for ketamine in pregnancy and lactation are limited. It should only be used when the potential benefit justifies any possible risk to the fetus or infant, and decisions should be made by the treating physician.

To order Ketalar, 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 and necessary import documentation.

Ketalar differs from agents such as propofol by providing dissociative anesthesia and preserving airway reflexes, while also producing analgesia. It has a distinct cardiovascular profile, often increasing blood pressure and heart rate, whereas propofol typically causes hypotension.

Ketalar should be stored at ambient temperature, protected from light and moisture, and kept in its original packaging. Do not freeze the product, and ensure that the container is sealed when not in use.

Ketalar is supplied as a sterile injectable solution and can be given either intravenously or intramuscularly. Administration is performed by qualified healthcare professionals in a controlled clinical environment, with continuous monitoring of vital signs.

Serious risks include respiratory depression, laryngospasm, severe hypertension, and rare allergic reactions such as anaphylaxis. Prompt recognition and supportive measures are essential when these events occur.

Ketalar should be avoided in patients with known hypersensitivity to ketamine, uncontrolled severe hypertension, or conditions where increased intracranial or intra‑ocular pressure is contraindicated. Clinicians must assess each patient individually before use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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