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<p style="text-align: left; "> <b></b> </p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>AMPIVET </b><b><sup></sup></b><b>K forte</b> |
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</p> |
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<p style="text-align: left; "> intramamarna suspenzija </p> |
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<p style="text-align: left; "> </p> |
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</div> |
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<div align="Left"> |
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<p style="text-align: left; "> <b>Za uporabo v veterinarski medicini</b> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Sestava</b> </p> |
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<p style="text-align: left; "> 1 injektor (= 5 ml suspenzije) vsebuje: </p> |
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<div align="Left"> |
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<p style="text-align: left; "> 75 mg ampicilina v obliki ampicilin natrija |
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</p> |
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<div align="Left"> |
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<p style="text-align: left; "> 200 mg kloksacilina v obliki kloksacilin |
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natrija </p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Delovanje</b> </p> |
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<div align="Left"> |
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<p style="text-align: left; "> Ampivet K forte je kombinacija polsintetiènih |
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penicilinov <sup>_</sup> ampicilina in kloksacilina. Oba antibiotika pri |
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obèutljivih bakterijah zavirata preèno povezovanje peptidoglikanskih |
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niti in v fazi njihovega narašèanja delujeta baktericidno. Ampivet |
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K deluje antimikrobno proti najpomembnejšim povzroèiteljem mastitisa |
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s po Gramu pozitivnimi in po Gramu negativnimi bakterijami, kot so: <i>Streptococcus |
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agalactiae, Streptococcus disgalactiae, Streptococcus uberis, Staphylococcus |
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aureus, E. coli, Corynebacterium pyogenes </i>idr. Pri tem oba penicilina |
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ka¾eta aditiven in delno tudi sinergistièen uèinek. |
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Ker je kloksacilin odporen proti bakterijski betalaktamazi, s tem pripravkom |
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uspešno zdravimo vnetja, ki jih povzroèajo soji stafilokokov, odpornih |
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proti benzilpenicilinu. Intramamarno dajanje Ampiveta K forte v vime ima |
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baktericidni uèinek, ne da bi izzvalo lokalno dra¾enje tkiva. |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Indikacije</b> </p> |
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<p style="text-align: left; "> Zdravljenje kliniènih in subkliniènih |
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mastitisov pri kravah v laktaciji. </p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Kontraindikacije</b> </p> |
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<p style="text-align: left; "> Zdravila ne smemo dajati ¾ivalim, |
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obèutljivim za penicilinske antibiotike. </p> |
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<p style="text-align: left; "> Ne smemo zdraviti krav med presušitvijo. |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Stranski uèinki</b> </p> |
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<p style="text-align: left; "> Niso znani. </p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Naèin dajanja in odmerki</b> </p> |
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<p style="text-align: left; "> <i>Krave</i> </p> |
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<p style="text-align: left; "> Oboleli predel je treba umiti in vršièek |
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seska dezinficirati, nato injektorjev nastavek vnesemo v sesni kanal, kamor |
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iztisnemo njegovo vsebino. V oboleli predel vimena je treba iztisniti vsebino |
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enega injektorja. </p> |
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<p style="text-align: left; "> Dajanje zdravila je dvakratno po presledku |
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12 ur. </p> |
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<p style="text-align: left; "> Pri hujših infekcijah priporoèamo |
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dajanje zdravila ne samo v oboleli predel, temveè po 1 injektor tudi |
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v preostale dele vimena. </p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Karenca</b> </p> |
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<p style="text-align: left; "> Meso: 7 dni </p> |
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<p style="text-align: left; "> Mleko: 3 dni </p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Opozorilo</b> </p> |
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<p style="text-align: left; "> Ni priporoèljivo soèasno intramamarno |
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ali parenteralno dajanje tetraciklinov, makrolidov ali kloramfenikola. </p> |
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<p style="text-align: left; "> Èe so ¾ivali preobèutljive |
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za penicilinske antibiotike, se lahko na zdravilo odzovejo alergièno. |
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</p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Naèin shranjevanja</b> </p> |
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<p style="text-align: left; "> Shranimo pri temperaturi do 15 <sup>o</sup> |
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C in nedosegljivo otrokom. </p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Naèin izdajanja</b> </p> |
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<p style="text-align: left; "> Na recept. </p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Rok uporabnosti</b> </p> |
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<p style="text-align: left; "> Oznaèen na ovojnini (2 leti). </p> |
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<p style="text-align: left; "> <b>Postopek s prazno ovojnino</b> </p> |
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<p style="text-align: left; "> Ostanke zdravila in prazno ovojnino je treba |
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obravnavati kot posebne odpadke in jih ni dovoljeno odmetavati med obièajne |
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komunalne odpadke. </p> |
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<p style="text-align: left; "> <b>Oprema</b> </p> |
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<p style="text-align: left; "> Škatla z 12 injektorji </p> |
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<p style="text-align: left; "> </p> |
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<p style="text-align: left; "> <b>Številka in datum odloèbe</b> </p> |
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<p style="text-align: left; "> 323-03-8/00-139, 06.08.2001 </p> |
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<p style="text-align: left; "> <b>Proizvajalec</b> </p> |
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<p style="text-align: left; "> VETERINA d.o.o., HRVAŠKA </p> |
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<p style="text-align: left; "> <b>Zastopnik</b> </p> |
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<div align="Justify"> |
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<p style="text-align: justify; "> PLIVA LJUBLJANA d. o. o., SLOVENIJA </p> |
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<p style="text-align: left; "> <b>Revidirano na sej</b><b>i Komisije za |
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registracijo zdravil za uporabo v veterinarski medicini dne 26.01.2001.</b> |
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<b></b> </p> |
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