Product image of Ketanest S (Esketamine Hydrochloride) supplied by GNH India

Ketanest S

Active Ingredient:
Esketamine Hydrochloride
Origin:
EU

Ketanest S (Esketamine Hydrochloride)

Esketamine hydrochloride, the active ingredient in Ketanest S, is a NMDA receptor antagonist presented as a 50 mg/mL injectable solution for intramuscular and intravenous use. It provides rapid induction of general anesthesia, procedural sedation, and analgesia in adult patients undergoing surgical or diagnostic procedures.

GNH India supplies Ketanest S as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide. The company adheres to global quality standards and provides regulatory‑approved batches to healthcare institutions across multiple regions. It also ensures timely delivery and post‑market support.

Manufacturer / TM Owner

Pfizer Corporation Austria Ges.M.B.H.

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Indications & Clinical Uses

  • Esketamine hydrochloride, an NMDA receptor antagonist, is employed in anesthesia and sedation pathways.
  • Induction of general anesthesia: produces rapid unconsciousness and amnesia for surgical procedures.
  • Procedural sedation: provides safe, controllable sedation for diagnostic or minor surgical interventions.
  • Analgesia: delivers effective pain relief during and after operative procedures.

How It Works

  • Esketamine hydrochloride acts as a non‑competitive antagonist at the N‑methyl‑D‑aspartate (NMDA) receptor, binding within the ion channel and preventing calcium influx. This blockade disrupts excitatory neurotransmission, leading to dissociative anesthesia and analgesia. The drug also modulates opioid receptors and influences monoaminergic pathways, contributing to its analgesic and sedative properties without significant respiratory depression. Additionally, it reduces central sensitization to painful stimuli.

Side Effects

Esketamine may be associated with a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Hypertension: transient increase in blood pressure.
  • Tachycardia: elevated heart rate.
  • Nausea: feeling of sickness.
  • Vomiting: expulsion of stomach contents.
  • Dissociation: sense of detachment from environment.
  • Psychomimetic symptoms: vivid dreams or hallucinations.

Serious or Rare Side Effects

  • Respiratory depression: reduced breathing effort.
  • Seizures: convulsive episodes.
  • Severe hypertension: sustained high blood pressure.
  • Allergic reactions: rash, itching, anaphylaxis.

Precautions & Warnings

  • When using Ketanest S, clinicians should observe several safety measures to minimize risk.
  • Patient assessment: evaluate cardiovascular status and airway before administration.
  • Monitoring: continuously observe blood pressure, heart rate, and oxygen saturation during the procedure.
  • Drug interactions: avoid concurrent use with other central nervous system depressants unless closely supervised.
  • Contraindications: do not use in patients with known hypersensitivity to esketamine or other NMDA antagonists.
  • Pregnancy and lactation: consider potential risks as safety data are limited; use only if benefits outweigh risks.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Esketamine can interact with other medications, affecting its safety profile or efficacy.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of hypertensive crisis.
  • CYP2B6 inhibitors (e.g., clopidogrel): may increase esketamine plasma levels.
  • Other NMDA antagonists: additive dissociative effects.

Moderate Interactions (Monitor Closely)

  • CNS depressants (benzodiazepines, opioids): may enhance sedation and respiratory depression.
  • Sympathomimetic agents (e.g., epinephrine): may exacerbate hypertension.
  • Serotonergic drugs (SSRIs, SNRIs): monitor for serotonin syndrome signs.

Frequently Asked Questions

Ketanest S is an injectable formulation of esketamine hydrochloride used by anesthesiologists to induce rapid general anesthesia, provide procedural sedation, and deliver analgesia during surgical or diagnostic interventions.

Esketamine acts as a non‑competitive antagonist at the NMDA receptor, blocking calcium influx and disrupting excitatory neurotransmission. This produces dissociative anesthesia and analgesia, while also modulating opioid and monoaminergic pathways to enhance its sedative effects.

The dose of Ketanest S is determined by the prescribing clinician based on the patient’s age, weight, medical condition, and the required depth of anesthesia. Dosing is individualized and should follow the institution’s anesthesia protocols.

Safety data for esketamine in pregnancy and lactation are limited. The product is classified as having an unknown pregnancy category, so it should only be used when the potential benefits justify any possible risk to the fetus or infant.

To order Ketanest S, submit an enquiry on the product page at gnhindia.com with 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 any necessary import documentation.

Ketanest S contains esketamine, the S‑enantiomer of ketamine, which generally offers a higher potency and a more favorable side‑effect profile than racemic ketamine. Both provide dissociative anesthesia, but esketamine may require lower doses and produce fewer psychomimetic reactions.

Ketanest S should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Use aseptic technique when drawing the solution into syringes, and keep the product in its original packaging until use.

Ketanest S is administered by a trained healthcare professional either intravenously or intramuscularly. The injection is performed under continuous monitoring of vital signs, and the dose is titrated to achieve the desired depth of anesthesia or sedation.

The most serious risks associated with Ketanest S include respiratory depression, severe hypertension, seizures, and rare allergic reactions such as anaphylaxis. Continuous monitoring of airway, breathing, and cardiovascular status is essential during administration.

Ketanest S should be avoided in patients with known hypersensitivity to esketamine or other NMDA antagonists, those with uncontrolled hypertension, severe cardiovascular disease, or a history of seizures unless the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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