Vetoryl 10 mg hard capsules for dogs

Country: Ireland

Bahasa: Inggeris

Sumber: HPRA (Health Products Regulatory Authority)

Beli sekarang

Ciri produk Ciri produk (SPC)
12-06-2017

Bahan aktif:

Trilostane

Boleh didapati daripada:

Dechra Ltd

Kod ATC:

QH02CA01

INN (Nama Antarabangsa):

Trilostane

Dos:

10 Milligrams per capsule

Borang farmaseutikal:

Capsule, hard

Jenis preskripsi:

POM: Prescription Only Medicine as defined in relevant national legislation

Kumpulan terapeutik:

Dogs

Kawasan terapeutik:

trilostane

Tanda-tanda terapeutik:

Hormone

Status kebenaran:

Authorised

Tarikh kebenaran:

2010-10-01

Ciri produk

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Vetoryl 10 mg hard capsules for dogs.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Hard capsule.
Ivory body and black cap with the capsule strength printed on the body
of the capsule.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Dogs.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
In dogs: for the treatment of pituitary-dependent and
adrenal-dependent hyperadrenocorticism (Cushing’s disease and
syndrome).
4.3 CONTRAINDICATIONS
Do not use in animals suffering from primary hepatic disease and/or
renal insufficiency.
Do not use in dogs weighing less than 3 kg.
Do not use where there is suspected hypersensitivity to the active
substance or to any of the excipients.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
An accurate diagnosis of hyperadrenocorticism is essential.
Where there is no apparent response to treatment, the diagnosis should
be re-evaluated. Dose increases may be
necessary.
Veterinarians should be aware that dogs with hyperadrenocorticism are
at increased risk of pancreatitis. This risk may
not diminish following treatment with trilostane.
1 capsule contains:
Active substance: Trilostane
10 mg
Excipients:
Titanium dioxide (E171)
0.942 mg
Ferric oxide (yellow) (E172)
0.035 mg
Ferric oxide (black) (E172)
0.532 mg
For a full list of excipients, see section 6.1.
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