KETATHESIA
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
KETATHESIA (Ketamine HCl Injection, USP)CIIIVeterinary Injection for Intramuscular Use in Cats and Subhuman Primates Only
ANADA 200-073, Approved by FDA
FEDERAL LAW RESTRICTS THIS DRUG TO USE BY OR ON THE ORDER OF A LICENSED VETERINARIAN.
COLOR OF SOLUTION MAY VARY FROM COLORLESS TO VERY SLIGHTLY YELLOWISH AND MAY DARKEN UPON PROLONGED EXPOSURE TO LIGHT. THIS DARKENING DOES NOT AFFECT POTENCY. DO NOT USE IF PRECIPITATE APPEARS.
NOT MORE THAN 0.1 MG/ML BENZETHONIUM CHLORIDE ADDED AS A PRESERVATIVE.
KETATHESIA (Ketamine HCl Injection, USP) is a rapid-acting, nonnarcotic, nonbarbiturate agent for anesthetic use in cats and for restraint in subhuman primates. It is chemically designated dl2-(ochlorophenyl)-2-(methylamino) cyclohexanone hydrochloride and is supplied as a slightly acid (pH 3.5 to 5.5) solution for intramuscular injection in a concentration containing the equivalent of 100 mg ketamine base per milliliter and contains not more than 0.1 mg/mL benzethonium chloride as a preservative.
ACTION
KETATHESIA is a rapid-acting agent whose pharmacological action is characterized by profound analgesia, normal pharyngeal-laryngeal reflexes, mild cardiac stimulation and respiratory depression. Skeletal muscle tone is variable and may be normal, enhanced or diminished. The anesthetic state produced does not fit into the conventional classification of stages of anesthesia, but instead KETATHESIA produces a state of unconsciousness which has been termed "dissociative" anesthesia in that it appears to selectively interrupt association pathways to the brain before producing somesthetic sensory blockade.
In contrast to other anesthetics, protective reflexes, such as coughing and swallowing are maintained under KETATHESIA anesthesia. The degree of muscle tone is dependent upon level of dose; therefore, variations in body temperature may occur. At low dosage levels there may be an increase in muscle tone and a concomitant slight increase in body temperature. However, at high dosage levels there is some diminution in muscle tone and a resultant decrease in body temperature, to the point where supplemental heat may be advisable.
In cats, there is usually some transient cardiovascular stimulation, increased cardiac output with slight increase in mean systolic pressure with little or no change in total peripheral resistance. At higher doses, the respiratory rate is usually decreased.
The assurance of a patent airway is greatly enhanced by virtue of maintained pharyngeal-laryngeal reflexes. Although some salivation is occasionally noted, the persistence of the swallowing reflex aids in minimizing the hazards associated with ptyalism. Salivation may be effectively controlled with atropine sulfate in dosages of 0.04 mg/kg (0.02 mg/lb) in cats and 0.01 to 0.05 mg/kg (0.005 to 0.025 mg/lb) in subhuman primates.
Other reflexes, e.g., corneal, pedal, etc., are maintained during KETATHESIA anesthesia, and should not be used as criteria for judging depth of anesthesia. The eyes normally remain open with the pupils dilated. It is suggested that a bland ophthalmic ointment be applied to the cornea if anesthesia is to be prolonged.
Following administration of recommended doses, cats become ataxic in about 5 minutes with anesthesia usually lasting from 30 to 45 minutes at higher doses. At the lower doses, complete recovery usually occurs in 4 to 5 hours but with higher doses recovery time is more prolonged and may be as long as 24 hours.
In studies involving 14 species of subhuman primates represented by at least 10 anesthetic episodes for each species, the median time to restraint ranged from 1.5 [Aotus trivirgatus (night monkey) and Cebus capucinus (white-throated capuchin)] to 5.3 minutes [Macaca nemestrina (pig-tailed macaque)]. The median duration of restraint ranged between 20 and 55 minutes in all but five of the species studied. Total time from injection to end of restraint ranged from 43 [Saimiri sciureus (squirrel monkey)] to 183 minutes [Macaca nemestrina (pigtailed macaque)] after injection. Recovery is generally smooth and uneventful. The duration is dose related.
By single intramuscular injection, KETATHESIA usually has a wide margin of safety in cats and subhuman primates. In cats, cases of prolonged recovery and death have been reported.
Uses
INDICATIONS
KETATHESIA may be used in cats for restraint or as the sole anesthetic agent for diagnostic or minor, brief, surgical procedures that do not require skeletal muscle relaxation. It may be used in subhuman primates for restraint.
CONTRAINDICATIONS
KETATHESIA is contraindicated in cats and subhuman primates suffering from renal or hepatic insufficiency.KETATHESIA is detoxified by the liver and excreted by the kidneys; therefore, any preexistent hepatic or renal pathology or impairment of function can be expected to result in prolonged anesthesia; related fatalities have been reported.
PRECAUTIONS
In cats, doses in excess of 50 mg/kg during any single procedure should not be used. The maximum recommended dose in subhuman primates is 40 mg/kg.
To reduce the incidence of emergence reactions, animals should not be stimulated by sound or handling during the recovery period. However, this does not preclude the monitoring of vital signs.
Apnea, respiratory arrest, cardiac arrest and death have occasionally been reported with ketamine used alone, and more frequently when used in conjunction with sedatives or other anesthetics. Close monitoring of patients is strongly advised during induction, maintenance and recovery from anesthesia.
ADVERSE REACTIONS
Respiratory depression may occur following administration of high doses of KETATHESIA. If at any time respiration becomes excessively depressed and the animal becomes cyanotic, resuscitative measures should be instituted promptly. Adequate pulmonary ventilation using either oxygen or room air is recommended as a resuscitative measure.Adverse reactions reported have included emesis, salivation, vocalization, erratic recovery and prolonged recovery, spastic jerking movements, convulsions, muscular tremors, hypertonicity, opisthotonos, dyspnea and cardiac arrest. In the cat, myoclonic jerking and/or mild tonic convulsions can be controlled by ultrashortacting barbiturates which should be given to effect. The barbiturates should be administered intravenously at a dose level of one-sixth to one-fourth the usual dose for the product being used. Acepromazine may also be used. However, recent information indicates that some phenothiazine derivatives may potentiate the toxic effects of organic phosphate compounds such as found in flea collars and certain anthelmintics. A study has indicated that ketamine hydrochloride alone does not potentiate the toxic effects of organic phosphate compounds.
ADMINISTRATION AND DOSAGE
KETATHESIA is well tolerated by cats and subhuman primates when administered by intramuscular injection.
Fasting prior to induction of anesthesia or restraint with KETATHESIA is not essential; however, when preparing for elective surgery, it is advisable to withhold food for at least six hours prior to administration of KETATHESIA.
Anesthesia may be of shorter duration in immature cats. Restraint in subhuman primate neonates (less than 24 hours of age) is difficult to achieve.
As with other anesthetic agents, the individual response to KETATHESIA is somewhat varied depending upon the dose, general condition and age of the subject so that dosage recommendations cannot be absolutely fixed.
DosageCats:
Subhuman Primates: Cercocebus torquatus Papio cynocephalusPantroglodytes verusPapio anubisPongo pygmaeusMacaca nemestrinaPresbytis entellusGorilla gorilla gorillaAotus trivirgatusMacaca mulattaCebus capucinusMacaca fascicularisMacaca radiataSaimiri sciureus
A single intramuscular injection produces restraint suitable for TB testing, radiography, physical examination or blood collection.
HOW SUPPLIED
KETATHESIA is supplied as the hydrochloride in concentrations equivalent to ketamine base.
Each 10 mL vial contains 100 mg/mL.
NDC 11695 0700 1 - 10 mL vial
CLINICAL STUDIES
KETATHESIA has been clinically studied in subhuman primates in addition to those species listed under Administration and Dosage. Dosages for restraint in these additional species, based on limited clinical data, are: Cercopithecus aethiops (grivet), Papio papio (guinea baboon) 10 to 12 mg/kg; Erythrocebus patas patas (patas monkey) 3 to 5 mg/kg; Hylobates lar (white-handed gibbon) 5 to 10 mg/kg; Lemur catta (ringtailed lemur) 7.5 to 10 mg/kg; Macaca fuscata (Japanese macaque) 5 mg/kg; Macaca speciosa (stumptailed macaque) and Miopithecus talapoin (mangrove monkey) 5 to 7.5 mg/kg; and Symphalangus syndactylus (siamangs) 5 to 7 mg/kg.
Manufactured for Putney, Inc.
Distributed By
Principal Display Panel - 10 mL vial
BUTLER SCHEIN ANIMAL HEALTH - A Henry Schein Company
PUTNEY
NDC 11695-0700-1
KETATHESIA™
Ketamine HCl Injection USP
CIII
Equivalent to 100 mg/mL Ketamine
ANADA #200-073, APPROVED BY FDA
CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Net Contents: 10 mL
Distributed Exclusively by
Butler Schein Animal Health
Dublin, OH 43017
www.butlerschein.com
83307677, R.O
REORDER #043012
Principal Display Panel - 144 vial shipper
KETATHESIA™
Ketamine HCl Injection, USP
100 mg/mL
QTY: 144 Vials (12 Packs of 12)
Lot: 12345WW
NDC 11695-0700-1
Exp: MMM YYYY
ANADA #200-073
Distributed by:
Butler Schein Animal Health
Dublin, OH 43017
Made in USA
83307758, R.1
KETATHESIAketamine hydrochloride INJECTION, SOLUTION
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