DOLETHAL 200 MG/ML SOLUTION FOR INJECTION

Ülke: İrlanda

Dil: İngilizce

Kaynak: HPRA (Health Products Regulatory Authority)

Aktif bileşen:

PENTOBARBITAL SODIUM

Mevcut itibaren:

Vetoquinol Ireland Limited

ATC kodu:

QN51AA01

INN (International Adı):

PENTOBARBITAL SODIUM

Doz:

200 Mg/Ml

Farmasötik formu:

Solution for Injection

Reçete türü:

VPO-Vet.Practitioner Only

Terapötik grubu:

Canine, Feline

Terapötik alanı:

Pentobarbital

Terapötik endikasyonlar:

Neurological Preparations

Yetkilendirme durumu:

Authorised

Yetkilendirme tarihi:

1990-10-01

Ürün özellikleri

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Dolethal 200 mg/ml Solution for Injection
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Solution for injection.
A red aqueous solution.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Dogs, cats.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Euthanasia of dogs and cats.
4.3 CONTRAINDICATIONS
Not for anaesthetic use.
Not for use in animals intended for animal or human consumption.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
It may be necessary to increase the dose for older animals weighing more than 10 kg.
Each ml contains:
Active substance
Pentobarbital Sodium
200 mg
Excipients
Benzyl Alcohol
0.0104 ml
Cochineal Red A (E124)
0.01 mg
For a full list of excipients, see section 6.1
HEALTH PRODUCTS REGULATORY AUTHORITY
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_Date Printed 14/08/2015_
_CRN 7021600_
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4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
None.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE MEDICINAL PRODUCT TO ANIMALS
Lethal to humans.
Particular care should be taken to avoid accidental exposure to the product.
In the case of accidental self-administration (injection, ingestion, skin absorption), seek URGENT medical attention,
advising medical services of barbiturate poisoning.
In the case of accidental contact with eyes, irrigate eyes immediately with flowing cold or tepid water.
In the case of contact with skin, wash immediately with water and then thoroughly with soap and water.
4.6 ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
None.
4.7 USE DURING PREGNANCY, LACTATION OR LAY
Not relevant.
4.8 INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF INTERACTION
None.
4