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The average amount required to produce 5 to 10 minutes of surgical anesthesia within 30 seconds following injection is 2 mg/kg. Administer Ketalar slowly (i.e., over a period of 60 seconds). Rapid administration may result in respiratory depression and enhanced vasopressor response. The induction dose may be administered as an.
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The initial dose of KETALAR administered intravenously may range from 1 mg/kg to 4.5 mg/kg. The average amount required to produce 5 to 10 minutes of surgical anesthesia within 30 seconds following injection is 2 mg/kg. Administer KETALAR slowly (i.e., over a period of 60 seconds). Rapid
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Ketalar is recommended: 1. as the sole anaesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. Ketalar is best suited for short procedures and it can be used with additional doses, for longer procedures; 2. for the induction of anaesthesia prior to the administration of other general anaesthetic agents, and 3. to supplement low-potency agents.
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KETALAR contains the active ingredient ketamine hydrochloride. KETALAR belongs to a group of medicines called anaesthetics and is used to make the body insensitive to surgical treatment. It may be used in combination with other medicines to induce anaesthesia. For more information, see Section 1. Why am I being treated with KETALAR? in the full.
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DESCRIPTION. Ketalar is a nonbarbiturate anesthetic chemically designated dl 2-(0-chlorophenyl)-2-(methylamino) cyclohexanone hydrochloride. It is formulated as a slightly acid (pH 3.5-5.5) sterile solution for intravenous or intramuscular injection in concentrations containing the equivalent of either 10, 50 or 100 mg ketamine base per milliliter and contains not more than 0.1 mg/mL Phemerol.
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WHEN KETALAR IS USED ON AN OUTPATIENT BASIS, THE PATIENT SHOULD NOT BE RELEASED UNTIL RECOVERY FROM ANESTHESIA IS COMPLETE AND THEN SHOULD BE ACCOMPANIED BY A RESPONSIBLE ADULT. DESCRIPTION KETALAR is a nonbarbiturate general anesthetic chemically designated dl 2-(0-chlorophenyl)-2 (methylamino) cyclohexanone hydrochloride.
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Ketalar 10mg/ml Solution for Injection/Infusion. Pfizer Healthcare Ireland PA0822/013/001. Main Information.. Kevin O'Malley House, Earlsfort Centre, Earlsfort Terrace, Dublin 2, Ireland, D02 XP77 +353 (1) 676 4971; [email protected] Follow @TheHPRA . Developed by Engine Solutions.
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When fluid restriction is required, KETALAR can be added to a 250 mL infusion as described above to provide a KETALAR concentration of 2 mg/mL. KETALAR 10 mg/mL vials are not recommended for dilution. 3 DOSAGE FORMS AND STRENGTHS. KETALAR injection is a clear, colorless, sterile solution available in multiple-dose vials containing.
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Ketalar 10mg/ml contains 53 mg of sodium per 20 ml of solution. For the full list of excipients see section 6.1. 3. Pharmaceutical form. An intravenous dose of 2 mg/kg of bodyweight usually produces surgical anaesthesia within 30 seconds after injection and the anaesthetic effect usually lasts 5 to 10 minutes. An intramuscular dose of 10 mg.
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KETALAR is used for one dose in one patient only. Any remaining contents should be discarded. Product description What it looks like KETALAR is a clear colourless solution in a glass vial. Ingredients KETALAR contains 200 mg/2 mL of ketamine as hydrochloride as the active ingredient. It also contains: benzethonium chloride (phemerol)
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Ketalar should not be used if the solution is coloured and/or contains particulate matter. 6.5 Nature and Contents of Container. Ketalar 200 mg (base)/2 mL, 5 x 2 mL glass vials. 6.6 Special Precautions for Disposal. In Australia, any unused medicine or waste material should be disposed of in accordance with local requirements.
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KETALAR 200 mg/2 mL, 5 x 2 mL vials. Australian Registration Number: AUST R 70073. Who distributes KETALAR. Pfizer Australia Pty Ltd Sydney NSW Toll Free Number: 1800 675 229 www.pfizer.com.au. This leaflet was prepared in September 2021. Keep Reading. What we're talking about.
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Coadministration with other CNS depressants, such as skeletal muscle relaxants, may cause respiratory depression, hypotension, profound sedation, coma, and/or death. Consider dose reduction of either or both agents to avoid serious adverse effects. Monitor for hypotension, respiratory depression, and profound sedation.
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KETALAR 200 mg/2 mL, 5 x 2 mL vials. Australian Registration Number: AUST R 70073. Who distributes KETALAR. Pfizer Australia Pty Ltd. Sydney NSW. Toll Free Number: 1800 675 229.
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Ketalar may cause serious side effects. Call your doctor at once if you have: painful or difficult urination, increased urination, loss of bladder control, blood in your urine; a light-headed feeling, like you might pass out; slow heart rate, weak or shallow breathing; or. jerky muscle movements that may look like convulsions.
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The onset of action of KETALAR is rapid; an intravenous dose of 2 mg/kg of body weight usually produces surgical anaesthesia within 30 seconds after injection, with the anaesthetic effect usually lasting 5 to 10 minutes. If a longer effect is desired, additional increments can be administered intravenously or intramuscularly.