TOLFEDINE 60 MG TABLETS

Ülke: İrlanda

Dil: İngilizce

Kaynak: HPRA (Health Products Regulatory Authority)

Aktif bileşen:

TOLFENAMIC ACID

Mevcut itibaren:

Vetoquinol Ireland Limited

ATC kodu:

QM01AG02

INN (International Adı):

TOLFENAMIC ACID

Doz:

60 mg/tablet

Farmasötik formu:

Tablets

Reçete türü:

POM

Terapötik grubu:

Canine

Terapötik alanı:

Tolfenamic acid

Terapötik endikasyonlar:

N.S.A.I.D

Yetkilendirme durumu:

Authorised

Yetkilendirme tarihi:

1993-08-12

Ürün özellikleri

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Tolfedine 60 mg tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains:
ACTIVE SUBSTANCE
Tolfenamic Acid
60mg
For a full list of excipients see section 6.1.
3 PHARMACEUTICAL FORM
Tablet
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Dogs
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Treatment of acute inflammation due to chronic locomotor disease.
4.3 CONTRAINDICATIONS
Concurrent administration with other steroidal or non-steroidal anti-inflammatory drugs.
Do not use in animals with suspected gastro-duodenal ulceration.
Do not use in animals with impaired renal or hepatic function.
Do not use in pregnant animals.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
HEALTH PRODUCTS REGULATORY AUTHORITY
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_Date Printed 14/08/2015_
_CRN 7021600_
_page number: 1_
4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTION(S) FOR USE IN ANIMALS
Do not exceed the stated dose or duration of treatment.
Use in any animal less than 6 weeks of age or in aged animals may involve additional risk. If such use cannot be avoided,
careful clinical management is essential. Reduced metabolism and excretion in these animals should be considered.
Avoid use in any dehydrated, hypovolaemic or hypotensive animal as there is a potential risk of increased renal toxicity.
It is preferable that TOLFEDINE is not administered to animals undergoing general anaesthesia until fully recovered.
Where there is appearance of bloody or black faeces, a veterinary surgeon should be contacted for advice and the
possibility of stopping treatment should be considered.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE VETERINARY MEDI