EN - Anglická CZ - Česká SK - Slovenská PL - Polská RO - Rumunská RU - Ruská TR - Turecká UA - Ukrajinská
EN - Anglická
  • CZ - Česká
  • SK - Slovenská
  • PL - Polská
  • RO - Rumunská
  • RU - Ruská
  • TR - Turecká
  • UA - Ukrajinská

NARKAMON 100 mg/ml solution for injection

Homepage Products Veterinary products NARKAMON 100 mg/ml solution for injection

Ketamin. Short term general anaesthesia in dogs, cats, horses and donkeys for diagnostic and therapeutic procedures

type of preparative: Analeptic, anaesthetic, hypnotics
target species animals: Dog, Cat, Horse

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1 ml of clear, colourless solution for injection contains:

Active ingredient: ketaminum 100 mg (as ketamine hydrochloride 115.4 mg)

Excipients:

Benzethonium-chloride                  0.10 mg
Disodium - edetate (dihydrate)       0.10 mg

INDICATION:

Short term general anaesthesia in dogs, cats, horses and donkeys for diagnostic and therapeutic procedures.

CONTRAINDICATION:

Pregnancy, cardiovascular insufficiency, hypertension, liver and kidney insufficiency, epilepsy. Application of ketamine in horses for unmanageable excitation.

ADVERSE REACTIONS:

High doses could result in respiratory depression.

TARGET SPECIES:

Dogs, cats, horses and donkeys.


DOSAGE:

Method of administration: intramuscular or intravenous.
The dosage should be adjusted individually to individual patients.

Horse

The usual dose is 2 ml of the product / 100 kg of live weight  (i.e. 2 mg of ketamine/kg of live weight) quickly intravenously.
NARKAMON 100 mg/ml solution for injection is suitable to lay down the animal, for shorter general anaesthesia, or for the initiation of inhalation anaesthesia in horses. The horse lies down spontaneously.
To extend or possibly to enhance the general anaesthesia may be administered an additional same dose.
For safe effect of ketamine is required sedative premedication e.g. acepromazin 0.1 mg/kg of live weight, then guaifenesine 90-120 mg/kg of live weight or xylazine 0.4-0.6 mg/kg of live weight i.v.

Dog

Monoanaesthesia 0.1-0.2 ml of the product/kg of live weight (i.e. 10 - 20 mg of ketamine/kg of live weight) intramuscularly
Combination options: atropin 0.05 mg/kg of live weight i.v., i.m., s.c. together with acepromazine in a dose of 0.1 mg/kg of live weight, after initiation of their effect NARKAMON 100 mg/ml solution for injection in a dose
of 0.2 ml/10 kg of live weight. (i.e. 2 mg of ketamine/kg of live weight) intravenously
Another option: atropin 0.05 mg/kg of live weight together with xylazine in a dose of 2 mg/kg of live weight i.m., after initiation of their effect NARKAMON 100 mg/ml solution for injection in a dose of 0.05 - 0.1 ml/kg of live weight. (i.e. 5 - 10 mg of ketamine/kg of live weight) intramuscularly

Cat

Monoanaesthesia 0.2-0.4 ml of the product/kg of live weight (i.e. 20 - 40 mg of ketamine/kg of live weight) intramuscularly
Combined anaesthesia: 0.1-0.2 ml of the product/kg of live weight (i.e. 10 - 20 mg of ketamine/kg of live weight) intramuscularly
Combination options: to reduce salivation atropin in a dose of 0.05 mg/kg of live weight together with acepromazine in a dose of 0.1 - 0.15 mg/kg of live weight.
After onset of their effect NARKAMON 100 mg/ml of solution for injection in a dose of 0.2 ml/kg of live weight (i.e. 20 mg of ketamine/kg of live weight) intramuscularly or atropin together with xylazine in a dose
of 2 mg/kg of live weight i.m., s.c. and after initiation of their effect NARKAMON 100 mg/ml solution for injection in a dose of 0.1 ml/kg of live weight. (i.e. 10 mg of ketamine/kg of live weight) intramuscularly.

ADVICE ON CORRECT ADMINISTRATION:

Intravenous administration is recommended in large animals.
The plug is tested for up to 50 punctures.

WITHDRAWAL PERIOD:

Not intended for food-producing animals.Do not use in horses and donkeys, meat and milk of which is intended for human consumption.

SPECIAL STORAGE PRECAUTIONS:

Keep out of the reach of children. Keep the vial in a box, protected against light.
Protect from frost. Do not use after the expiry date stated on the carton.
Shelf life after the first opening of the package: 28 days.

SPECIAL WARNING(S):

Special warnings for use in animals
The animal needs to be properly examined before the actual administration.
Special precautions to be taken by the persons administering the veterinary medicinal product to animals
This veterinary medicinal product is characterized by very strong effects. Avoid accidental self injection. Protect the needle till the moment of product administration.
Avoid contact of the product with the eyes and skin.
In case of contact with skin, immediately wash affected site with sufficient amount of water and remove contaminated clothing and shoes.
In case of eye contact, immediately wash the affective eye with large amount of water.  In case of adverse reactions, seek medical advice.
In case of an accidental ingestion of the preparation, drink large amount of water, seek medical advice immediately and show the package insert or label to the treating physician. DO NOT DRIVE MOTOR VEHICLES
In case of an accidental self administration of the preparation, seek medical advice immediately and show the package insert or label to the treating physician. DO NOT DRIVE MOTOR VEHICLES
Do not smoke, eat and drink during administration.
The product should not be administered by pregnant and breastfeeding women, elderly, patients with cardiac problems, individuals with circulatory and respiratory problems and diabetic patients.

Package

10 ml, 50 ml


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