Soloxine 0.2 mg Tablet

Country: Irlanda

Lingwa: Ingliż

Sors: HPRA (Health Products Regulatory Authority)

Ingredjent attiv:

Levothyroxine sodium

Disponibbli minn:

Virbac S.A.

Kodiċi ATC:

QH03AA01

INN (Isem Internazzjonali):

Levothyroxine sodium

Dożaġġ:

0.2 mg/tablet

Għamla farmaċewtika:

Tablet

Tip ta 'preskrizzjoni:

POM: Prescription Only Medicine as defined in relevant national legislation

Grupp terapewtiku:

Dogs

Żona terapewtika:

levothyroxine sodium

Indikazzjonijiet terapewtiċi:

Hormone

L-istatus ta 'awtorizzazzjoni:

Authorised

Data ta 'l-awtorizzazzjoni:

2007-01-19

Karatteristiċi tal-prodott

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Soloxine 0.2 mg Tablet
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
ACTIVE SUBSTANCE
Levothyroxine Sodium
0.20 mg
EXCIPIENTS
Sunset Yellow FCF E110
0.1 mg
For a full list of excipients see section 6.1.
3 PHARMACEUTICAL FORM
Small elliptical orange tablets.
Scored on the face of each tablet, strength in milligrams to the right
and the word SOLOXINE on the reverse.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Dogs.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the long term treatment of thyroid insufficiency in dogs.
4.3 CONTRAINDICATIONS
Do not use in animals with known hypersensitivity to the active
ingredient.
Do not use in animals suffering from thyrotoxicosis or uncorrected
adrenal insufficiency
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
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4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTION(S) FOR USE IN ANIMALS
Appropriate laboratory tests should be conducted to confirm the
diagnosis and ensure correct dosage.
Caution should be exercised in the treatment of dogs with clinically
significant cardiac disease, hypertension or any
disease rendering the animal susceptible to sharply increased
metabolic rate.
In such cases, consideration should be
given to reducing the starting dose, increasing the dose at inte