Ketalar50 mg/ml

Ketalar 50 mg/ml is recommended for: As the sole anesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. Ketalar 50 mg/ml is best suited for short procedures and it can be used with additional doses, for longer procedures. For the induction of anesthesia prior to the administration of other general anesthetic agents. To supplement low-potency agents, such as nitrous oxide. 

General (Intravenous) anesthetics

Ketalar 50 mg/ml is a noncompetitive N-methyl-D-aspartate receptor antagonist that blocks glutamate. It has a direct action on the cortex and limbic system. It produces a cataleptic-like state wherein the patient is withdrawn from the surrounding environment.

Adult:General Anesthesia- IV Induction: 1-4.5 mg/kg single dose IM Induction: 6.5-13mg IV Infusion: 1-2mg/kg at 0.5mg/kg/min Maintenance: The maintenance dose should be adjusted according to the patient's anesthetic needs and whether an additional anesthetic is employed. Increments of one-half to the full induction dose may be repeated as needed for maintenance of anesthesia.Rapid sequence Intubation, Induction - 2mg/kg IVPediatric:General Anesthesia: IV Induction: 1-2 mg/kg IV; range: 4-13 mg/kg IM Induction: 5-10 mg/kg; range: 0.5-4.5 mg/kg Maintenance: 0.01-0.03 mg/kg/min continuous IV infusion Maintenance: The maintenance dose should be adjusted according to the patient's anesthetic needs and whether an additional anesthetic is employed. Increments of one-half to the full induction dose may be repeated as needed for maintenance of anesthesia.

Rate of Administration: It is recommended that Ketalar 50 mg/ml should be administered slowly (over a period of 60 seconds). More rapid administration may result in respiratory depression and enhanced pressor response.The 100 mg/ml concentration of Ketalar 50 mg/ml should not be injected intravenously without proper dilution. It is recommended the drug be diluted with an equal volume of either Sterile Water for Injection, USP, Normal Saline, or 5% Dextrose in Water.

Prolonged recovery time with barbiturates or narcotics. May potentiate neuromuscular blocking effects of atracurium and tubocurarine including resp depression with apnoea. May increase risk of bradycardia, hypotension or decreased cardiac output with halogenated anaesthetics. May potentiate CNS depression and risk of resp depression with CNS depressants (e.g. phenothiazines, sedating H1-blockers, skeletal muscle relaxants). May antagonise hypnotic effect of thiopental. May increase risk of HTN with thyroid hormones. May increase risk of hypotension with antihypertensive agents. Reduction in seizure threshold resulting in unpredictable extensor-type seizures when given concurrently with theophylline.

CV disease including severe HTN; patients with increased intraocular or CSF pressure.

Emergence reactions (e.g. vivid dreams, hallucinations, confusion, irrational behaviour); increased muscle tone sometimes resembling seizures; temporary HTN and tachycardia, hypotension, bradycardia, arrhythmias, apnoea, laryngospasm, resp depression, diplopia, nystagmus, nausea, vomiting, lacrimation, hypersalivation, raised intraocular and CSF pressure, transient rash and pain at inj site, cystitis.

Pregnancy: The safe use of Ketalar 50 mg/ml in pregnancy has not been established, and such use is not recommended.Lactation: Ketalar 50 mg/ml is likely to be excreted in breast milk and therefore breastfeeding should be discontinued when Ketalar 50 mg/ml is in use.

Patient with cardiac decompensation, chronic alcoholic or acutely alcohol-intoxicated patients, pre-anaesth elevated CSF pressure, globe injuries, increased intraocular pressure (e.g. glaucoma), neurotic traits or psychiatric illness (e.g. schizophrenia, acute psychosis), acute intermittent porphyria, seizures, hyperthyroidism, pulmonary or upper resp infection, intracranial mass lesions, head injury, or hydrocephalus, hypovolaemia, dehydration, cardiac disease esp coronary artery disease (e.g. CHF, myocardial ischaemia, MI). Pregnancy and lactation.

Symptoms: Resp depression. Management: Employ supportive ventilation. Mechanical support of respiration is preferred to admin of analeptics.

Store between 20-25° C.

To prepare a dilute solution containing 1 mg of Ketalar 50 mg/ml per ml, aseptically transfer 10 ml (50 mg per ml vial) to 500 ml of Dextrose Injection, 5% or Sodium Chloride Injection, 0.9% and mix well. The resultant solution will contain 1 mg of Ketalar 50 mg/ml per ml.