PERMAWAY 600 mg intramammary suspension for cattle

Šalis: Airija

kalba: anglų

Šaltinis: HPRA (Health Products Regulatory Authority)

Nusipirk tai dabar

Parsisiųsti Prekės savybės (SPC)
24-04-2021
Parsisiųsti DSU (DSU)
08-01-2023

Veiklioji medžiaga:

Cloxacillin Benzathine

Prieinama:

Vetoquinol Ireland Limited

ATC kodas:

QJ51CF02

INN (Tarptautinis Pavadinimas):

Cloxacillin Benzathine

Dozė:

600 milligram(s)

Vaisto forma:

Intramammary suspension

Recepto tipas:

POM: Prescription Only Medicine as defined in relevant national legislation

Gydymo sritis:

cloxacillin

Autorizacija statusas:

Authorised

Leidimo data:

2021-04-23

Prekės savybės

                                Health Products Regulatory Authority
23 April 2021
CRN009FKH
Page 1 of 4
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
PERMAWAY 600 mg intramammary suspension for cattle
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each intramammary syringe (3.6 g) contains:
ACTIVE SUBSTANCE:
Cloxacillin (as benzathine) 600 mg
EXCIPIENTS:
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Intramammary suspension.
Shiny white to off-white viscous suspension.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Dairy cattle (dry cows).
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the treatment of subclinical mastitis at dry-off and prevention of
new intramammary infections occurring during the dry
period, caused by _Trueperella pyogenes, Staphylococcus spp.,
Streptococcus agalatiae, Streptococcus dysgalactiae _and_ _
_Streptococcus uberis_, susceptible to cloxacillin.
4.3 CONTRAINDICATIONS
Do not use in cases of known hypersensitivity to penicillins,
cephalosporins, or to any of the excipients. Do not use in cows with
clinical mastitis outside the dry period.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
4.5 SPECIAL PRECAUTIONS FOR USE
This product does not contain any antimicrobial preservatives.
Special precautions for use in animals
Use of the product should be based on susceptibility testing of
bacteria isolated from milk samples obtained from the udder
quarter(s) of each cow to be dried off. If this is not possible,
therapy should be based on local (regional, farm level) risk based
epidemiological information about the expected pathogen challenge, and
susceptibility of target bacteria.
Use of the product deviating from the instructions given in the SPC
may contribute to the development of bacterial resistance
to cloxacillin which may also decrease the effectiveness of treatment
with other beta-lactamase resistant penicillins. Dry cow
therapy protocols should take local and national policies on
antimicrobial use into consideration, and undergo regular
veterinary review.
                                
                                Perskaitykite visą dokumentą
                                
                            

Ieškokite perspėjimų, susijusių su šiuo produktu