Country: New Zealand
Bahasa: Inggeris
Sumber: Ministry for Primary Industries
carbimazole
Schering-Plough Animal Health Limited
carbimazole
carbimazole 100 g/kg
Endocrine agent (hormone)
ACVM Registered
2011-06-14
VIDALTA 10 30 and 100 tablets – Leaflet, Carton and Label Page 1 of 7 Vidalta 10 26-Mar-20 Leaflet DANGER RESTRICTED VETERINARY MEDICINE KEEP OUT OF THE REACH OF CHILDREN FOR ANIMAL TREATMENT ONLY VIDALTA ® 10 100 MG TABLETS FOR CATS (CONTAINING 10 MG OF CARBIMAZOLE) VIDALTA 10 are round pink tablets, each containing 10 mg carbimazole and 0.25 mg red ferric oxide (E 172). READ ENTIRE LEAFLET BEFORE USE. INDICATIONS For the treatment of hyperthyroidism and hyperthyroidism-associated clinical signs in cats. DIRECTIONS FOR USE DOSAGE AND ADMINISTRATION For oral use only. VIDALTA 10 tablets should be administered at the same time every day, in particular with relation to feeding. Do not break or crush VIDALTA 10 tablets as this will affect the sustained release properties of the tablet. The prolonged release formulation of VIDALTA 10 enables a 24-hour dosing interval. The aim of treatment is to maintain total thyroxin concentrations (TT4) in the lower end of the reference range. Accordingly, the following dose recommendations for dosing during adjustment and maintenance phases are suggested. However, dosing adjustment should be primarily based upon the clinical assessment of the individual cat. Monitoring of TT4, full haematology and liver and kidney parameters is advised at each recommended follow up visit. Adjustment phase The starting dose is a single daily oral administration of one tablet of Vidalta 15 (A011752, 15 mg carbimazole) per cat. Consideration could be given to a starting dose of VIDALTA 10 (10 mg carbimazole) daily where the TT4 concentration is only mildly increased, e.g. between 50 nmol/L and 100 nmol/L. With the recommended starting dose of one Vidalta 15 tablet once daily, total thyroxin concentration (TT4) may decrease to within the euthyroid range (TT4<50 nmol/L) shortly after treatment initiation. A dose adjustment may be required as early as 10 days after commencing treatment. Dose adjustment should be also performed 3, 5 and 8 weeks after initiation of treatment, depending on both clinical Baca dokumen lengkap