ZOLETIL 100 (50 mg/ml + 50 mg/ml) lyophilisate and solvent for solution for injection for dogs and cats

Država: Irska

Jezik: engleski

Izvor: HPRA (Health Products Regulatory Authority)

Kupi sada

Svojstava lijeka Svojstava lijeka (SPC)
05-02-2023
DSU DSU (DSU)
05-02-2023

Aktivni sastojci:

Tiletamine; Zolazepam

Dostupno od:

Virbac S.A.

ATC koda:

QN01AX99

INN (International ime):

Tiletamine; Zolazepam

Doziranje:

100 milligram(s)/millilitre

Farmaceutski oblik:

Lyophilisate and solvent for solution for injection

Tip recepta:

POM: Prescription Only Medicine as defined in relevant national legislation

Terapijska grupa:

Cats, Dogs

Područje terapije:

other general anesthetics, combinations

Terapijske indikacije:

Anaesthetic/Analgesic

Status autorizacije:

Authorised

Datum autorizacije:

2016-04-15

Svojstava lijeka

                                2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
ZOLETIL 100 (50 mg/ml+50 mg/ml) lyophilisate and solvent for solution
for injection for dogs and
cats
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each vial of 970 mg lyophilisate contains:
Active substances:
Tiletamine (as hydrochloride)
250.00 mg
Zolazepam (as hydrochloride)
250.00 mg
Each vial of 5 ml solvent contains:
Benzyl alcohol (E1519)
0.100 g
Water for injections
5.00 ml
Each ml of reconstituted solution contains:
Active substances:
Tiletamine (as hydrochloride)
50.00 mg
Zolazepam (as hydrochloride)
50.00 mg
Excipient:
Benzyl alcohol (E1519)
20.00 mg
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Lyophilisate and solvent for solution for injection.
Appearance of the lyophilisate: White to slightly yellow compact mass;
Appearance of the solvent: Clear colourless liquid;
Appearance of the reconstituted solution: Clear, colourless to
slightly green-yellow solution, free from
particles.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Dogs and cats.
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
General anaesthesia.
4.3
CONTRAINDICATIONS
Do not use in cases of hypersensitivity to the active substances or to
any of the excipients.
Do not use in animals with severe cardiac or respiratory disease, or
in animals with renal, pancreatic or
hepatic insufficiency.
Do not use in the event of severe hypertension.
Do not use in rabbits.
Do not use in animals with head trauma or intracranial tumours.
Do not use for caesarean section.
Do not use in pregnant bitches and queens.
3
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
In dogs, since zolazepam is eliminated more quickly than tiletamine,
there is a shorter duration of
tranquilisation than there is of anaesthesia.
4.5
SPECIAL PRECAUTIONS FOR USE
i) Special precautions for use in animals
Animals should be fasted for 12 hours prior to anaesthesia.
Remove anti-parasite collar 24 hours before anaesthesia.
If necessary, hypersalivation can be controlled with the
administration of anticholinergic agent
                                
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