Label: ISOFLURANE liquid

WARNING: Not for use in horses intended for food

Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Isoflurane, USP is a nonflammable, nonexplosive general inhalation anesthetic agent. Its chemical name is l-chloro-2,2,2-trifluoroethyl difluoromethyl ether, and its structural formula is:

Each mL contains 99.9% isoflurane.

Some physical constants are:

**Equation for vapor pressure calculation:

log10Pvap= A + B/T        where:             A = 8.056

                                                               B = -1664.58

                                                               T = °C + 273.16 (Kelvin)

MAC (Minimum Alveolar Concentration) is 1.31% in horses1 and 1.28% in dogs.6

Isoflurane is a clear, colorless, stable liquid containing no additives or chemical stabilizers. Isoflurane has a mildly pungent, musty, ethereal odor. Samples stored in indirect sunlight in clear, colorless glass for five years, as well as samples directly exposed for 30 hours to a 2 amp, 115 volt, 60 cycle long wave U.V. light were unchanged in composition as determined by gas chromatography. Isoflurane in one normal sodium methoxide-methanol solution, a strong base, for over six months consumed essentially no alkali, indicative of strong base stability. Isoflurane does not decompose in the presence of soda lime (at normal operating temperatures), and does not attack aluminum, tin, brass, iron or copper.

Isoflurane is an inhalation anesthetic. Induction and recovery from anesthesia with isoflurane are rapid.2,5  The level of anesthesia may be changed rapidly with isoflurane.  Isoflurane is a profound respiratory depressant.  RESPIRATION MUST BE MONITORED CLOSELY IN THE HORSE AND DOG AND SUPPORTED WHEN NECESSARY.  As anesthetic dose is increased, both tidal volume and respiratory rate decrease.3,6  This depression is partially reversed by surgical stimulation, even at deeper levels of anesthesia.

Blood pressure decreases with induction of anesthesia but returns toward normal with surgical stimulation.  Progressive increases in depth of anesthesia produce corresponding decreases in blood pressure; however, heart rhythm is stable and cardiac output is maintained with controlled ventilation and normal PaCO2 despite increasing depth of anesthesia.  The hypercapnia which attends spontaneous ventilation during isoflurane anesthesia increases heart rate and raises cardiac output above levels observed with controlled ventilation.3  Isoflurane does not sensitize the myocardium to exogenously administered epinephrine in the dog.

Muscle relaxation may be adequate for intra-abdominal operations at normal levels of anesthesia. However, if muscle relaxants are used to achieve greater relaxation, it should be noted that: ALL COMMONLY USED MUSCLE RELAXANTS ARE MARKEDLY POTENTIATED WITH ISOFLURANE, THE EFFECT BEING MOST PROFOUND WITH THE NONDEPOLARIZING TYPE.  Neostigmine reverses the effect of nondepolarizing muscle relaxants in the presence of isoflurane but does not reverse the direct neuromuscular depression of isoflurane. 

Isoflurane is used for induction and maintenance of general anesthesia in horses and dogs.

Isoflurane is contraindicated in horses and dogs with known sensitivity to isoflurane or to other halogenated agents.

Increasing depth of anesthesia with isoflurane may increase hypotension and respiratory depression.  The electroencephalographic pattern associated with deep anesthesia is characterized by burst suppression, spiking, and isoelectric periods.4

Since levels of anesthesia may be altered easily and rapidly, only vaporizers producing predictable percentage concentrations of isoflurane should be used.  (See DOSAGE AND ADMINISTRATION).

The action of nondepolarizing relaxants is augmented by isoflurane.  Less than the usual amounts of these drugs should be used.  If the usual amounts of nondepolarizing relaxants are given, the time for recovery from myoneural blockade will be longer in the presence of isoflurane than in the presence of other commonly used anesthetics.

Not for use in horses intended for food.

Keep out of reach of children.

Isoflurane, like other inhalational anesthetics, can react with desiccated carbon dioxide (CO2) absorbents to produce carbon monoxide which may result in elevated carboxyhemoglobin levels in some patients. Case reports suggest that barium hydroxide lime and soda lime become desiccated when fresh gases are passed through the CO2 absorber canister at high flow rates over many hours or days.  When a clinician suspects that CO2 absorbent may be desiccated, it should be replaced before the administration of isoflurane.

Usage in pregnancy:  Reproduction studies have been performed in mice and rats with no evidence of fetal malformation attributable to isoflurane.  Adequate data concerning the safe use of isoflurane in pregnant and breeding horses and dogs have not been obtained.

Hypotension, respiratory depression, and arrhythmias have been reported. 

In the event of overdosage, or what may appear to be overdosage, the following action should be taken:

Stop drug administration, establish that the airway is clear and initiate assisted or controlled ventilation with pure oxygen as circumstances dictate.

Caution: Operating rooms should be provided with adequate ventilation to prevent the accumulation of anesthetic vapors.

Premedication: A premedication regimen, which may be employed depending upon the patient status, to avert excitement during induction, might include an anticholinergic, a tranquilizer, a muscle relaxant, and a short-acting barbiturate.

Inspired concentration: The delivered concentration of isoflurane should be known.  Isoflurane may be vaporized using a flow-through vaporizer specifically calibrated for isoflurane.  Vaporizers delivering a saturated vapor which is then diluted (e.g. Vernitrol® vaporizer) also may be used.  The delivered concentration from such a vaporizer may be calculated using the formula:

% Isoflurane =  100 PVFV

                        FT (PA – PV)

where:            

PA = Pressure of atmosphere

PV = Vapor pressure of isoflurane

FV = Flow of gas through vaporizer (mL/min)

FT = Total gas flow (mL/min)

Isoflurane contains no stabilizer. Nothing in the drug product alters calibration or operation of these vaporizers.

Induction:

Horses: Inspired concentrations of 3.0% to 5.0% isoflurane alone with oxygen following a barbiturate anesthetic induction are usually employed to induce surgical anesthesia in the horse.

Dogs: Inspired concentrations of 2.0% to 2.5% isoflurane alone with oxygen following a barbiturate anesthetic induction are usually employed to induce surgical anesthesia in the dog.

These concentrations can be expected to product surgical anesthesia in 5 to 10 minutes.

Maintenance:  The concentration of vapor necessary to maintain anesthesia is much less than that required to induce it.

Horses: Surgical levels of anesthesia in the horse may be sustained with a 1.5% to 1.8% concentration of isoflurane in oxygen.

Dogs:  Surgical levels of anesthesia in the dog may be sustained with a 1.5% to 1.8% concentration of isoflurane in oxygen.

The level of blood pressure during maintenance is an inverse function of isoflurane concentration in the absence of other complicating problems. Excessive decreases, unless related to hypovolemia, may be due to depth of anesthesia and in such instances may be corrected by lightening the level of anesthesia. 

Recovery from isoflurane anesthesia is typically uneventful.2

Isoflurane, USP is packaged in 100 mL (NDC 11695-6777-1) and 250 mL (NDC 11695-6777-2) amber-colored bottles.

Storage:

Store at room temperature 20oC to 25oC (68oF to 77oF); excursions permitted to 15°C to 30°C (59°F to 86°F) [See USP Controlled Room Temperature].

1. Steffey, E.P., Howland, D. Jr., Giri, S. and Eger, E.I. II.: Enflurane, halothane and isoflurane potency in horses. Am. J. Vet. Res. 1977; 38(7): 1037-1039.
2. Auer, J.A., Garner, H.E., Amend, J.F., Hutcheson, D.P. and Salem, C.A., Recovery from anesthesia in ponies: A comparative study of the effects of isoflurane, enflurane, methoxyflurane and halothane. Equine Vet. J. 1978; 10(1): 18-23.
3. Steffey, E.P. and Howland, D. Jr., Comparison of circulatory and respiratory effects of isoflurane and halothane anesthesia in horses. Am. J. Vet. Res. 1980; 41(5): 821-825.
4. Auer, J.A., Amend, J.F., Garner, H.E., Hutcheson, D.P. and Salem, C.A., Electroencephalographic responses during volatile anesthesia in domestic ponies: A comparative study of isoflurane, enflurane, methoxyflurane, and halothane. Equine Practice. 1979:3:130-134.
5. Klide, A.M., Cardiopulmonary effects of enflurane and isoflurane in the dog. Am. J. Vet. Res. 1976; 37(2): 127-131.
6. Steffey, E.P., and Howland, D. Jr., Isoflurane potency in the dog and cat. Am. J. Vet. Res. 1977; 38(11): 1833-1936.

Text revised: January 2023

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Dublin, OH 43017
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Product of India

To report suspected adverse drug events, for technical assistance or to obtain a copy of the Safety Data Sheet, contact Covetrus® at

1-855-724-3461. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS, or online at http://www.fda.gov/reportanimalae.

Approved by FDA under ANADA # 200-237

Label

NDC: 11695-6777-1

Isoflurane, USP

100mL

A nonflammable, nonexplosive
inhalation anesthetic
For use in horses and dogs

Label

NDC: 11695-6777-2

Isoflurane, USP

250mL

A nonflammable, nonexplosive
inhalation anesthetic
For use in horses and dogs