PHOSPHONORTONIC 20 % INJECTABLE SOLUTION

Nazione: Irlanda

Lingua: inglese

Fonte: HPRA (Health Products Regulatory Authority)

Principio attivo:

TOLDIMFOS SODIUM TRIHYDRATE

Commercializzato da:

Vetoquinol Ireland Limited

Codice ATC:

QA12CX90

INN (Nome Internazionale):

TOLDIMFOS SODIUM TRIHYDRATE

Dosaggio:

20 %w/v

Forma farmaceutica:

Solution for Injection

Tipo di ricetta:

LM-Licensed Merchant

Gruppo terapeutico:

Bovine, Equine - Food

Area terapeutica:

Toldimfos

Indicazioni terapeutiche:

Vitamins & Minerals

Stato dell'autorizzazione:

Authorised

Data dell'autorizzazione:

1989-10-01

Scheda tecnica

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Phosphonortonic 20% Injectable Solution.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Solution for injection.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Horses, cattle.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Phosphonortonic supplies organic phosphorus and is indicated in the treatment of disorders of phosphorus metabolism in
horses and cattle.
4.3 CONTRAINDICATIONS
Do not use in case of hypersensitivity to the active substance.
Do not use the product in animals suffering from renal failure.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
None.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE VETERINARY MEDICINAL PRODUCT TO ANIMALS
None.
Each ml contains:
Active Substance
Toldimfos sodium trihydrate
20.00 % w/v
Excipients
Anhydrous Sodium Sulphite
0.20 % w/v
Phenethyl alcohol
1.00 % w/v
For a full list of excipients see 6.1
HEALTH PRODUCTS REGULATORY AUTHORITY
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_Date Printed 14/08/2015_
_CRN 7021600_
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4.6 ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
None known.
4.7 USE DURING PREGNANCY, LACTATION OR LAY
The product may be used in lactating animals.
No data are available on the effect of the product in pregnancy.
4.8 INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF INTERACTION
None known.
4.9 AMOUNTS TO BE ADMINISTERED AND ADMINISTRATION ROUTE
Administration is by intravenous and intramuscular routes in several sites.
The doses recommended may be repeated every 2 or 3 days or daily according to the severity of the case: 5 to 10 injections
in chronic affections.
Horses -