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Vetflurane 1000 Mg/G Inhalation Vapour, Liquid

Revised: February 2016

AN: 01092/2014

SUMMARY OF PRODUCT CHARACTERISTICS


1. NAME OF THE VETERINARY MEDICINAL PRODUCT


Vetflurane 1000 mg/g Inhalation vapour, liquid


2. QUALITATIVE AND QUANTITATIVE COMPOSITION


Each millilitre contains:

Active substance:

Isoflurane 1000 mg/g.


The veterinary medicinal product contains no excipients.


3. PHARMACEUTICAL FORM


Inhalation vapour, liquid

Clear, colourless liquid


4. CLINICAL PARTICULARS


4.1 Target species


Horses, dogs, cats, ornamental birds, reptiles, rats, mice, hamsters, chinchillas, gerbils, guinea pigs and ferrets.


4.2 Indications for use, specifying the target species


Induction and maintenance of general anaesthesia.


4.3 Contraindications


Do not use in case of known susceptibility to malignant hyperthermia.

Do not use in cases of known hypersensitivity to isoflurane or to other halogenated agents.


4.4 Special warnings


The metabolism of birds, and to an extent small mammals, is affected more profoundly by decreases in body temperature, due to high surface area to body weight ratio. Drug metabolism in reptiles is slow and highly dependent upon environmental temperature.


The absorption, distribution and elimination of isoflurane are rapid, and it is eliminated largely unchanged via the lungs. These characteristics may make it suitable for groups of patients including the young or old, or those with impaired hepatic, renal or cardiac function, however anaesthetic protocols should be decided on a case by case basis.

4.5 Special precautions for use


Special precautions for use in animals


Isoflurane has little or no analgesic properties. Adequate analgesia should always be given before surgery. The analgesic requirements of the patient should be considered before general anaesthesia is ended.


The use of the product in patients with cardiac disease should be considered only after a risk/ benefit assessment by the veterinarian.

It’s important to monitor breathing and pulse for the frequency and its features. It’s important to maintain airways free and properly oxygenate tissues during the maintenance of anaesthesia.

When using isoflurane to anaesthetise an animal with a head injury, consideration should be given as to whether artificial ventilation is appropriate to maintain normal CO2 levels, so that cerebral blood flow does not increase.


As isoflurane is a respiratory depressant, it could be advised to monitor the respiratory rate and depth during anaesthesia.


Special precautions to be taken by the person administering the veterinary medicinal product to animals


In case of a known hypersensitivity to isoflurane, the professional must not handle this product.

Do not breathe the vapour.

Users should consult their National Authority for advice on Occupational Exposure Standards for isoflurane.

Operating rooms and recovery areas should be provided with adequate ventilation or scavenging systems to prevent the accumulation of anaesthetic vapour. All scavenging/ extraction systems must be adequately maintained.

Pregnant and breast- feeding women should not have any contact with the product and should avoid operating rooms and animal recovery areas.

Avoid using masking procedures for prolonged induction and maintenance of general anaesthesia.

Use cuffed endotracheal intubation when possible for the administration of this product during maintenance of general anaesthesia.

To protect the environment, it is considered good practice to use charcoal filters with scavenging equipment.

Care should be taken when dispensing isoflurane, with any spillage removed immediately using an inert and absorbent material e.g. sawdust.

Wash any splashes from skin and eyes, and avoid contact with the mouth. If severe accidental exposure occurs remove the operator from the source of exposure, seek urgent medical assistance and show this label.

Halogenated anaesthetic agents may induce liver damage. In case of isoflurane this is an idiosyncratic response very rarely seen after repeated exposure.

Advice to Doctors: Ensure a patent airway and give symptomatic and supportive treatment. Note that adrenaline and catecholamines may cause cardiac dysrhythmias.

4.6 Adverse reactions (frequency and seriousness)


Isoflurane produces hypotension and respiratory depression in a dose- related manner. Cardiac arrhythmias and transient bradycardia have been reported only rarely.

Malignant hyperthermia has been reported very rarely in susceptible animals.

Respiratory arrest should be treated by assisted ventilation.

In the case of cardiac arrest, perform a complete cardio pulmonary resuscitation.


4.7 Use during pregnancy, lactation or lay


Pregnancy:

Use only according to the benefit/risk assessment by the responsible veterinarian. Isoflurane has been safely used for anaesthesia during caesarean section in the dog and cat.


Lactation:

Use only according to the benefit/risk assessment by the responsible veterinarian.


4.8 Interaction with other medicinal products and other forms of interaction


Concurrent inhalation of nitrous oxide enhances the effect of isoflurane in man and similar potentiation might be expected in animals.


The concurrent use of sedative or analgesic drugs is likely to reduce the level of isoflurane required to induce and maintain anaesthesia.


In horses, detomidine and xylazine have been reported to reduce MAC for isoflurane.


In dogs, morphine, oxymorphone, acepromazine, medetomidine plus midazolam have been reported to reduce the MAC for isoflurane. The concomitant administration of midazolam/ketamine during isoflurane anaesthesia may result in marked cardiovascular effects, particularly arterial hypotension. The depressant effects of propanolol on myocardial contractility are reduced during isoflurane anaesthesia, indicating a moderate degree of -receptor activity.


In cats, intravenous administration of midazolam-butorphanol has been reported to alter several cardio-respiratory parameters in isoflurane-induced cats as has epidural fentanyl and medetomidine. Isoflurane has been shown to reduce the sensitivity of the heart to adrenaline (epinephrine).


In cockatoos, butorphanol has been reported to reduce the MAC for isoflurane.

In pigeons, midazolam has been reported to reduce the MAC for isoflurane.


For reptiles and small mammals, there are no data available.


Isoflurane has a weaker sensitising action on the myocardium, to the effects of circulating dysrhythmogenic catecholamines, than halothane.


Isoflurane may be degraded to carbon monoxide by dried carbon dioxide absorbents.

4.9 Amounts to be administered and administration route


Isoflurane should be administered using an accurately calibrated vaporiser in an appropriate anaesthetic circuit, since levels of anaesthesia may be altered rapidly and easily.


Isoflurane may be administered in oxygen or oxygen/nitrous oxide mixtures.

The MAC (minimal alveolar concentration in oxygen) or effective dose ED50values and suggested concentrations given below for the target species should be used as a guide or starting point only. The actual concentrations required in practice will depend on many variables, including the concomitant use of other drugs during the anaesthetic procedure and the clinical status of the patient.


Isoflurane may be used in conjunction with other drugs commonly used in veterinary anaesthetic regimes for premedication, induction and analgesia. Some specific examples are given in the individual species information.


Recovery from isoflurane anaesthesia is usually smooth and rapid. The analgesic requirements of the patient should be considered before the termination of general anaesthesia.


The concurrent use of sedative or analgesic drugs is likely to reduce the level of isoflurane required to produce and maintain anaesthesia.


HORSE


The MAC for isoflurane in the horse is approximately 1.31%


Premedication


Isoflurane may be used with other drugs commonly used in veterinary anaesthetic regimes. The following drugs have been found to be compatible with isoflurane: acepromazine, butorphanol, detomidine, diazepam, dobutamine, dopamine, guaiphenesin, ketamine, morphine, pethidine, thiamylal, thiopentone and xylazine. Drugs used for premedication should be selected for the individual patient. However, the potential interactions below should be noted.


Interactions


See section 4.8.


Induction


As it is not normally practicable to induce anaesthesia in adult horses using isoflurane, induction should be by the use of a short acting barbiturate such as thiopentone sodium, ketamine or guaiphenesin. Concentrations of 3 to 5% isoflurane may then be used to achieve the desired depth of anaesthesia in 5 to 10 minutes


Isoflurane at a concentration of 3 to 5% in a high flow oxygen may be used for induction in foals.


Maintenance


Anaesthesia may be maintained using 1.5% to 2.5% isoflurane.


Recovery


Recovery is usually smooth and rapid.


DOG


The MAC for isoflurane in the dog is approximately 1.28%.


Premedication


Isoflurane may be used with other drugs commonly used in veterinary anaesthetic regimes. The following drugs have been found to be compatible with isoflurane: acepromazine, atropine, butorphanol, buprenorphine, bupivacaine, diazepam, dobutamine, ephedrine, epinephrine, glycopyrrolate, ketamine, medetomidine, midazolam, methoxamine, oxymorphone, propofol, thiamylal, thiopentone and xylazine. Drugs used for premedication should be selected for the individual patient. However, the potential interactions below should be noted.


Interactions


See section 4.8.


Induction


Induction is possible by face mask using up to 5% isoflurane, with or without premedication.


Maintenance


Anaesthesia may be maintained using 1.5% to 2.5% isoflurane.


Recovery


Recovery is usually smooth and rapid.


CAT


The MAC for isoflurane in the cat is approximately 1.63%.


Premedication


Isoflurane may be used with other drugs commonly used in veterinary anaesthetic regimes. The following drugs have been found to be compatible with isoflurane: acepromazine, atropine, diazepam, ketamine, and oxymorphone. Drugs used for premedication should be selected for the individual patient. However, the potential interactions below should be noted.


Interactions


See section 4.8.


Induction


Induction is possible by face mask using up to 4% isoflurane, with or without premedication.


Maintenance


Anaesthesia may be maintained using 1.5% to 3% isoflurane.


Recovery


Recovery is usually smooth and rapid.


ORNAMENTAL BIRDS


Few MAC/ED50values have been recorded. Examples are 1.34% for the Sandhill crane, 1.45% for the racing pigeon, reduced to 0.89% by the administration of midazolam, and 1.44% for cockatoos, reduced to 1.08% by the administration of butorphanol analgesic.


The use of isoflurane anaesthesia has been reported for many species, from small birds such as zebra finches, to large birds such as vultures, eagles and swans.


Drug interactions/compatibilities


Propofol has been demonstrated in the literature to be compatible with isoflurane anaesthesia in swans.


Interactions


See section 4.8.


Induction


Induction with 3 to 5% isoflurane is normally rapid. Induction of anaesthesia with propofol, followed by isoflurane maintenance, has been reported for swans.


Maintenance


The maintenance dose depends on the species and individual. Generally, 2 to 3% is suitable and safe.

Only 0.6 to 1% may be needed for some stork and heron species.

Up to 4 to 5% may be needed for some vultures and eagles.

3.5 to 4% may be needed for some ducks and geese.

Generally, birds respond very rapidly to changes in concentration of isoflurane.


Recovery


Recovery is usually smooth and rapid.


REPTILES


The literature records isoflurane’s use on a wide variety of reptiles (eg. various species of lizard, tortoise, iguanas, chameleon and snakes).

The ED50was determined in the desert iguana to be 3.14% at 35˚C and 2.83% at 20˚C.


Drug interactions/ compatibilities


See section 4.8.


Induction


Induction is usually rapid at 2 to 4% isoflurane.


Maintenance


1 to 3% is a useful concentration


Recovery


Recovery is usually smooth and rapid


RATS, MICE, HAMSTERS, CHINCHILLAS, GERBILS, GUINEA PIGS AND FERRETS


The MAC for mice has been cited as 1.34%, and for the rat as 1.38%, 1.46% and 2.4%.


Drug interactions/ compatibilities


See section 4.8.


Induction


Isoflurane concentration 2 to 3%.


Maintenance

Isoflurane concentration 0.25 to 2%.


Recovery


Recovery is usually smooth and rapid.


Species

MAC (%)

Induction (%)

Maintenance (%)

Recovery

Horse

1.31

3.0 – 5.0 (foals)

1.5 – 2.5

Smooth and rapid

Dog

1.28

Up to 5.0

1.5 – 2.5

Smooth and rapid

Cat

1.63

Up to 4.0

1.5 – 3.0

Smooth and rapid

Ornamental birds

See posology

3.0 – 5.0

See posology

Smooth and rapid

Reptiles

See posology

2.0 – 4.0

1.0 – 3.0

Smooth and rapid

Rats, mice, hamsters, chinchillas, gerbils, guinea pigs and ferrets

1.34 (mouse)

1.38/1.46/2.40 (rat)


2.0 – 3.0


0.25 – 2.0

Smooth and rapid


4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary


Isoflurane overdose may result in profound respiratory depression. Therefore, respiration must be monitored closely and supported when necessary with supplementary oxygen and/ or assisted ventilation.

In cases of severe cardiopulmonary depression, administration of isoflurane should be discontinued, the breathing circuit should be flushed with oxygen, the existence of a patent airway ensured, and assisted or controlled ventilation with pure oxygen initiated. Cardiovascular depression should be treated with plasma expanders, pressor agents, antiarrhythmic agents or other appropriate techniques.


4.11 Withdrawal period(s)


Horse: withdrawal period for meat and offal : 2 days.

The product should not be used for the treatment of mares producing milk for human consumption.


5. PHARMACOLOGICAL PROPERTIES


Pharmacotherapeutic group: Anaesthetic, general - halogenated hydrocarbons

ATCvet code: QN01AB06


5.1 Pharmacodynamic properties


Isoflurane produces unconsciousness by its action on the central nervous system. It has little or no analgesic properties.

Like other inhalation anaesthetics of this type, isoflurane depresses the respiratory and cardiovascular systems.


5.2 Pharmacokinetic particulars


Isoflurane is absorbed on inhalation and is rapidly distributed via the bloodstream to other tissues, including the brain. Its blood/gas partition coefficient at 37ْC is 1.4. The absorption and distribution of isoflurane and the elimination of non-metabolised isoflurane by the lungs are all rapid, with the clinical consequences of rapid induction and recovery and easy and rapid control of the depth of anaesthesia.

Metabolism of isoflurane is minimal (about 0.2%, mainly to inorganic fluoride) and almost all of the administered isoflurane is excreted unchanged by the lungs.


6. PHARMACEUTICAL PARTICULARS


6.1 List of excipients


None


6.2 Incompatibilities


Isoflurane has been reported to interact with dry carbon dioxide absorbents to form carbon monoxide. In order to minimise the risk of formation of carbon monoxide in rebreathing circuits and the possibility of elevated carboxyhaemoglobin levels, carbon dioxide absorbents should not be allowed to dry out.

6.3 Shelf life


Shelf-life of the veterinary medicinal product as packaged for sale: 2 years.


6.4. Special precautions for storage


Do not store above 25 C.

Protect from direct sunlight and heat.

Store in tightly closed original container.


6.5 Nature and composition of immediate packaging


The product is packaged in a cardboard box containing 100 ml or 250 ml amber coloured glass bottles (Type III) with low density polyethylene-lined caps.


Not all pack sizes may be marketed.


6.6 Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products


Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.


7. MARKETING AUTHORISATION HOLDER


Virbac

1ère avenue - 2065m - LID

06516 Carros

France


8. MARKETING AUTHORISATION NUMBER


Vm 05653/4166


9. DATE OF FIRST AUTHORISATION


16 September 2010


10. DATE OF REVISION OF THE TEXT


February 2016


Approved: 09 February 2016

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