Somulose Solution for Injection

Land: Ierland

Taal: Engels

Bron: HPRA (Health Products Regulatory Authority)

Werkstoffen:

Secobarbital sodium ; Cinchocaine Hydrochloride

Beschikbaar vanaf:

Dechra Ltd

ATC-code:

QN05CB02

INN (Algemene Internationale Benaming):

Secobarbital sodium ; Cinchocaine Hydrochloride

Dosering:

400/25 milligram(s)/millilitre

farmaceutische vorm:

Solution for injection

Prescription-type:

VPO: Veterinary Practitioner Only as defined in relevant national legislation

Therapeutische categorie:

Cats, Cattle, Dogs, Non food-producing horses

Therapeutisch gebied:

barbiturates in combination with other drugs

therapeutische indicaties:

Neurological Preparations

Autorisatie-status:

Authorised

Autorisatie datum:

2006-10-06

Productkenmerken

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Somulose Solution for Injection
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Solution for injection.
Clear slightly straw coloured viscous solution.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Dogs, cats, horses and cattle.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For euthanasia in dogs, cats, horses and cattle only.
4.3 CONTRAINDICATIONS
The combination product must not be used for anaesthesia, it is
non-sterile.
When used in horses or cattle do not use the carcass for animal
consumption.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
Non-vascular administration may delay onset of effect, cause pain and
result in excitement.
Rarely, horses may show resistance to euthanasia and prior use of
sedation should be considered in each case (see also
under section 4.9). It is always advisable to have an alternative
method of euthanasia available.
1 ml contains:
ACTIVE SUBSTANCES:
Secobarbital Sodium (Quinalbarbitone Sodium)
400 mg
Cinchocaine Hydrochloride
25
mg
For the full list of excipients, see section 6.1
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4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
Care should be taken not to excite the animal.
The dose is to be administered intravenously only (see also under
section