Vivitonin 50 mg film-coated tablets

Maa: Irlanti

Kieli: englanti

Lähde: HPRA (Health Products Regulatory Authority)

Aktiivinen ainesosa:

Propentofylline

Saatavilla:

Intervet Ireland Limited

ATC-koodi:

QC04AD90

INN (Kansainvälinen yleisnimi):

Propentofylline

Annos:

50 mg/tablet

Lääkemuoto:

Film-coated tablet

Prescription tyyppi:

POM: Prescription Only Medicine as defined in relevant national legislation

Terapeuttinen ryhmä:

Dogs

Terapeuttinen alue:

propentofylline

Käyttöaiheet:

Cardiovascular

Valtuutuksen tilan:

Authorised

Valtuutus päivämäärä:

1999-10-29

Valmisteyhteenveto

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Vivitonin 50 mg film-coated tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains:
ACTIVE SUBSTANCE:
Propentofylline
50 mg
EXCIPIENTS:
Titanium dioxide (E171)
0.359 mg
Yellow ferric oxide (E172)
0.125 mg
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Film-coated tablets.
Orange yellow round tablets, quarter scored on one side, with
‘K50’ embossed on the other side of the tablets.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Dogs.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the improvement of peripheral and cerebral vascular blood
circulation in dogs.
4.3 CONTRAINDICATIONS
None.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
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4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
In the case of specific diseases (e.g. kidney disease), appropriate
treatment should be administered.
Consideration should be given to rationalising the medication of dogs
already receiving treatment for congestive heart
disease or bronchial disease.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE
VETERINARY MEDICINAL
PRODUCT TO ANIMALS
Not applicable.
4.6 ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
In rare cases, symptoms of cardiac and cerebral over-