País: Irlanda
Idioma: anglès
Font: HPRA (Health Products Regulatory Authority)
Toldimfos sodium trihydrate
Vetoquinol Ireland Limited
QA12CX90
Toldimfos sodium trihydrate
20 percent weight/volume
Solution for injection
LM: Licensed Merchant as defined in relevant national legislation
Cattle, Horses
toldimfos
Vitamins and minerals
Authorised
1989-10-01
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 H E A L T H P R O D U C T S R E G U L A T O R Y A U T H O R I T Y ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ _D_ _a_ _t_ _e_ _ _ _P_ _r_ _i_ _n_ _t_ _e_ _d_ _ _ _1_ _4_ _/_ _0_ _8_ _/_ _2_ _0_ _1_ _5_ _C_ _R_ _N_ _ _ _7_ _0_ _2_ _1_ _6_ _0_ _0_ _p_ _a_ _g_ _e_ _ _ _n_ _u_ _m_ _b_ _e_ _r_ _:_ _ _ _1_ 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 Llegiu el document complet