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Presentation
A water soluble crystalline white powder and solvent for solution for injection. Each vial contains 583 mg xylazine hydrochloride. Each pack contains 1 vial of 50 ml of solvent which contains 0.70 mg/ml methyl hydroxybenzoate (Ph Eur) and 0.30 mg/ml propyl hydroxybenzoate (Ph Eur) as preservatives.
Uses
For use in horses and zoo animals where sedation is required, including—
1) Handling fractious animals, e.g. for transportation
2) Medical examinations, e.g. x-ray examination, removal of bandages, examination of teats, penis and oral cavity.
3) Premedication for minor superficial operations, painful manipulative procedures and local or regional anaesthesia.
Contra-indications, warnings, etc
Not for use in zoo animals intended for human consumption.
Caution is required when pulmonary disease is present or suspected.
In recumbent ruminants tympany should be prevented by maintaining sternal recumbency.
For operations on ruminants in lateral or dorsal recumbency it is advisable to lower the head and neck in order to avoid inhalation of saliva or ruminal fluids.
It must be noted that the swallowing reflex is reduced during the period when the action of the drug is at its peak.
When high doses are to be employed the animal should be fasted for some hours beforehand.
After high doses animals are likely to remain drowsy for several hours and should be kept in the shade.
In case of accidental overdosage leading to respiratory failure cold water douches and artificial respiration are indicated.
In the event of respiratory failure manual compression of the thorax is usually sufficient to restore normal respiration.
Following intravenous injection in horses there is a transient rise followed by a fall in blood pressure.
With horses and zoo animals the usual precautions required for handling should always be observed even when a high dose of Rompun has been given.
Transient hyperglycaemia is a common finding after Rompun sedation.
Operator Warnings
Xylazine is an alpha adrenoceptor agonist acting primarily on alpha-2 receptors.
Care should be taken to avoid accidental self-administration (see above).
It is recommended that once the required dose has been withdrawn from the vial, the needle should be kept guarded until the product is administered. Alternatively, it should be removed from the syringe and immediately inserted into the injection site and the syringe should then be connected to it.
Wash splashes from skin and eyes immediately.
In the event of accidental self-administration, seek medical advice and show the label and other product literature to medical staff. DO NOT DRIVE as changes in blood pressure may occur.
Information for Doctors
1.Human sedative dose: 0.3-0.6 mg/kg (1-2 ml Rompun 2%; 0.25-0.5 ml Rompun Dry Substance 10% solution).
2.Xylazine is an alpha adrenoceptor agonist whose toxicity may cause clinical effects including sedation, respiratory depression and coma, bradycardia, hypotension and hyperglycaemia. Ventricular arrhythmias have also been reported.
3.Treatment should be supportive with appropriate intensive therapy.
Withdrawal Periods
Horse
Meat:
Not to be used in horses intended for human consumption.
Treated horses may never be slaughtered for human consumption. The horse must have been declared as not intended for human consumption under national horse passport legislation.
Zoo Animals: Contra-indicated for animals intended for human consumption.
Pharmaceutical precautions
Do not store above 25°C
Store in a dry place.
Reconstitute the solution immediately before use.
Discard any unused solution.
Use solvent within 28 days of first broaching vial.
Do not use solvent if it becomes visibly contaminated.
Any unused product and containers should be disposed of in accordance with national requirements.
Further information
Xylazine, 5, 6-dihydro-2-(2, 6-xylidino)-4H-1, 3-thiazine, is a thiazine derivative with sedative, hypnotic, local anaesthetic and hypotensive properties. It also has muscle relaxant and analgesic effects; the degree of relaxation/analgesia depends upon the animal species.
Xylazine is an agonist of the alpha-2 adrenergic receptors. It acts on pre-synaptic and post-synaptic receptors of the central and peripheral nervous system. Both the sedation and the analgesia are due to stimulation of central alpha-2 adrenergic receptors.
Xylazine is absorbed extremely rapidly and distributed widely throughout tissues. After intramuscular injection maximum plasma concentrations are achieved within 12-14 minutes in all species.
Bioavailability varies after intramuscular injection; in the dog it is between 52 and 90%, in the sheep. 17-73% and in the horse 40-48%. Metabolism is extremely rapid. The molecule is broken down into several metabolites. Elimination after intramuscular and intravenous application takes place with a half-life of between 23 and 60 minutes depending on species. The half-life for total elimination, which is dependent on the route of administration and dosage, is 2-3 hours.
Analeptics will shorten the period or reduce the depth of sedation. Alpha-2 blockers such as atipamazole are effective in reversing the sedation and other physiological effects of the drug.
Legal category
POM-V (previously POM)
Packaging Quantities
Carton containing 5 bottles of 500 mg Xylazine and one 50 ml bottle of solvent each with a pierceable rubber stopper.
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Presentation
A clear colourless aqueous solution for injection. Each ml contains 23.32 mg xylazine hydrochloride (equivalent to 20 mg xylazine) and 1 mg methyl 4-hydroxybenzoate (E218) as a preservative.
Uses
Xylazine is an alpha-2 agonist with sedative, some analgesic and muscle relaxant properties, for use in cattle, horses, dogs and cats. In cattle, which are more sensitive to the agent, the degree of sedation can be predetermined according to the dose administered.
Indications: All cases where sedation is required including—
1) Handling fractious animals, e.g. for transportation
2) Medical examinations, e.g. x-ray examination, removal of bandages, examination of teats, penis and oral cavity.
3) Premedication for minor superficial operations, painful manipulative procedures and local or regional anaesthesia.
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Dosage and administration
Use two sterile needles one to fill the syringe from the bottle and one to inject the patient. Once the required dose has been withdrawn from the vial, the syringe should be removed from the needle. A separate sterile needle should be inserted into the injection site and the syringe connected to it. The needles should be discarded into a closed container.
Syringes and needles must be sterile. Clean area of injection site and swab with spirit.
Cattle
Rompun is given by intramuscular injection. The dose rate is 0.05–0.3 mg/kg (0.25–1.5 ml per 100 kg) bodyweight, according to the degree of sedation required. Very fractious animals may require the higher dose rates not exceeding 0.3 mg/kg (Dose rate 4)
Dose 1
Sedation, with a slight decrease of muscle tone. The ability to stand is maintained.
Dose 2
Sedation, marked decrease of muscle tone and some analgesia. The animal usually remains standing, but may lie down.
Dose 3
Deep sedation, further decrease of muscle tone and a degree of analgesia. The animal lies down.
Dose 4
Very deep sedation, a profound decrease in muscle tone and a degree of analgesia. The animal lies down.
Animals should not be disturbed until Rompun has taken its full effect. The first effects are usually seen within 5 minutes of injection and the maximum effect is produced ten minutes later. There is no struggling or excitement during induction or recovery.
If the required depth of sedation is not achieved, it is unlikely that repetition of the dose will prove more effective. It is advisable to allow complete recovery, repeating the procedure with a higher dose after 24 hours. When any surgical treatment is carried out using Rompun additional local anaesthesia should be employed.
When any surgical treatment is carried out using xylazine, additional local anaesthesia should be employed.
Horses
Administer by slow intravenous injection, taking from one to two minutes to administer. Dosage depends on the degree of sedation required and the response of the animal and is 0.6–1 mg/kg (3–5 ml/100 kg) bodyweight. Nervous or highly excitable horses generally require the higher dose. Experience has shown that older horses and those that have undergone severe exertion before treatment respond more readily to Rompun.
Depending on the dosage, light to deep sedation with individually variable analgesia is obtained. The horse does not become recumbent.
Animals should not be disturbed until Rompun has taken its full effect. This is usually obtained within 5 minutes of intravenous injection and lasts for approximately 20 minutes.
If the required depth of sedation is not achieved, it is unlikely that repetition of the dose will prove more effective. It is advisable to allow complete recovery, repeating the procedure using Rompun Dry Substance, with a higher dose rate, after 24 hours.
For operations and painful procedures, additional local or regional anaesthesia should be used.
Rompun can also be administered to horses as a premedicant for operations on the recumbent animal using chloral hydrate, barbiturates, ketamine or halothane.
Cats
Administer intramuscularly at a dose rate of 3 mg/kg (0.15 ml/kg) bodyweight. The effect is adequate for procedures that are not associated with any considerable degree of pain. Premedication with atropine is advantageous. When used in conjunction with ketamine, Rompun premedication eliminates muscular stiffness during anaesthesia and maintains sedation throughout the recovery period.
Barbiturate anaesthesia should not be induced until sedation is at its deepest, i.e. about 20 minutes after administration of Rompun. Under these conditions the dose of barbiturates is reduced by about half.
Dogs
Administer by intramuscular injection at a dose rate of 1–3 mg/kg (0.05–0.15 ml/kg) bodyweight. Other routes of administration may be used, but the effect is less predictable. Good sedation is usually achieved at the lower end of the dose range given above, but excitable or vicious animals require a higher dose. The effect is adequate for procedures that are not associated with any considerable degree of pain. For painful procedures use in combination with a local anaesthetic. Premedication with atropine may be advantageous.
When used for pre-anaesthetic medication, Rompun reduces the dose required in the case of barbiturates by about half. Rompun can also be used as a premedicant for ketamine induced anaesthesia.
Further Information Applicable to all Species
i)Analeptics will shorten the period or reduce the depth of sedation.
ii)Limited information available suggests tha alpha-2 blockers such as atipamezole may be effective in reversing the sedation and other physiological effects of the drug.
iii)Transient hyperglycaemia is a common finding after xylazine sedation.
Use During Pregnancy and Lactation
Do not use in the latter stages of pregnancy except at parturition. As the safety of xylazine use during organogenesis has not been fully demonstrated by current methods it should be used with caution during the first month of pregnancy.
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Contra-indications, warnings, etc
Observe aseptic precautions.
Do not use in horses intended for human consumption.
In the cat and dog, because of the emetic effect which is sometimes produced, do not use Rompun in mechanical complications of the alimentary tract e.g. obstruction of the oesophagus, gastric torsion or hernia.
Caution is required when pulmonary disease is present.
Tympany should be prevented in recumbent cattle by sternal recumbency.
For operations in lateral or dorsal recumbency, lower head and neck to prevent inhalation of ruminal contents.
Maintain recumbent and drowsy animals in the shade. In case of accidental overdosage leading to respiratory failure, cold water douches and artificial respiration are indicated.
Following intravenous injection in horses a transient rise and fall in blood pressure may be seen.
Sedated animals should remain under observation until normal. Segregate sedated animals.
The concurrent intravenous use of potentiated sulphonamides with alpha-2 agonists has been reported to cause cardiac arrhythmias which may be fatal. Whilst no such effects have been reported with Rompun, it is recommended that intravenous administration of Trimethoprim/Sulphonamide containing products should not be undertaken when horses have been sedated with xylazine.
In the event of respiratory failure manual compression of the thorax is usually sufficient to restore normal respiration.
In cats and dogs if the stomach is full, vomiting occurs before sedation is complete. This is an advantage if general anaesthesia is to follow. The emetic effect is reduced by fasting for 6 to 24 hours beforehand.
It must be noted that the swallowing reflex is reduced during the period when the action of the drug is at its peak.
After dose levels 3 and 4 cattle are likely to remain drowsy for several hours and should be kept in the shade.
Concurrent administration of adrenoceptor stimulants is not recommended.
Premedication with atropine in cats and dogs may reduce salivation and bradycardia effects.
Use with care in elderly or debilitated patients which may be adversely affected by profound cardiovascular changes.
Withdrawal Periods
Animals must not be slaughtered for human consumption during treatment.
Cattle: Meat: 6 daysCattle: Milk: 24 hours
Horse (meat): In accordance with the Horse Passport legislation (Commission Decision 2000/68/EC as implemented in national legislation), a 6 month withdrawal period applies to the use of this product
Operator Warnings
Xylazine is a powerful alpha-adrenergic agonist acting primarily on alpha-2 receptors.
Care should be taken to avoid accidental self-injection (see above).
It is recommended that, once the required dose has been withdrawn from the vial, the needle should be kept guarded until the product is administered. Alternatively it should be removed from the syringe and immediately inserted in the injection site, and the syringe should then be connected to it.
In the event of accidental self-administration, seek medical advice and show the product label and other product literature. DO NOT DRIVE as variations in blood pressure may be seen.
Wash splashes from skin and eyes immediately.
Pharmaceutical precautions
Do not store above 25°C.
Protect from light.
Following withdrawal of the first dose use the product within 28 days. Discard unused material.
Unused product and containers should be disposed of in accordance with any guidance from an appropriate waste regulation authority.
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Legal category
POM-V (previously POM)
Packaging Quantities
Bottles of 25 ml with pierceable rubber stoppers.
Further information
Xylazine is an alpha-2 agonist with sedative, some analgesic and muscle relaxant properties, for use in cattle, horses, dogs and cats. In cattle, which are more sensitive to the agent, the degree of sedation can be predetermined according to the dose administered. A strong emetic effect is usual in cats and dogs. Xylazine induces a strong cardiovascular effects e.g. bradycardia and increased blood pressure. Hyperglycaemia is also induced. The duration of action of the agent varies between species.
Analeptics will shorten the period or reduce the depth of sedation. Limited information available suggests that alpha-2 blockers such as atipamazole may be effective in reversing the sedation and other physiological effects of the drug.
A strong emetic effect is usual in cats and dogs. Xylazine induces strong cardiovascular effects e.g. bradycardia and increased blood pressure.
Transient hyperglycaemia is a common finding after Rompun sedation.
Marketing authorisation number
Vm 00010/4093.
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