Rilexine 500 Dry Cow

Hauptinformation

  • Handelsname:
  • Rilexine 500 Dry Cow Lösung zur intramammären Anwendung 63,09 mg/g
  • Dosierung:
  • 63,09 mg/g
  • Darreichungsform:
  • Lösung zur intramammären Anwendung
  • Verwenden für:
  • Tiere
  • Art der Medizin:
  • allopathic Droge

Dokumenten

  • Information für medizinisches Fachpersonal:
  • Das Informationsblatt für dieses Produkt ist derzeit nicht verfügbar, können Sie eine Anfrage an unseren Kundendienst zu senden und wir werden Sie benachrichtigen, sobald wir in der Lage, um es zu erhalten.


    Fordern Sie die Packungsbeilage für medizinisches Fachpersonal.

Lokalisierung

  • Erhältlich in:
  • Rilexine 500 Dry Cow Lösung zur intramammären Anwendung 63,09 mg/g
    Belgien
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • anti-bakterielle, Cephalosporine der ersten generation, cephalexin.

Weitere Informationen

Status

  • Quelle:
  • AFMPS - Agence Fédérale des Médicaments et des Produits de Santé - Belgium
  • Zulassungsnummer:
  • BE-V166162
  • Letzte Änderung:
  • 17-04-2018

Packungsbeilage

B. PACKUNGSBEILAGE

RILEXINE 500 Dry Cow Suspension zur intramammären Anwendung

1.

NAME UND ANSCHRIFT DES ZULASSUNGSINHABERS UND, WENN

UNTERSCHIEDLICH, DES HERSTELLERS, DER FÜR DIE CHARGENFREIGABE

VERANTWORTLICH IST

Zulassungsinhaber und Hersteller:der für die chargenfreigabe verantwortlich ist.

VIRBAC

1ère Avenue - 2065 m

L.I.D. - 06516 - CARROS

France

Vetrieb

VIRBAC BELGIUM

Esperantolaan 4

3001 LEUVEN

BELGIEN

2.

BEZEICHNUNG DES TIERARZNEIMITTELS

RILEXINE 500 Dry Cow Suspension zur intramammären Anwendung

3.

WIRKSTOFF UND SONSTIGE BESTANDTEILE

Wirkstoff

1 Injektor mit 8 g enthält 375 mg Cefalexin (als Benzathin)

(entsprechend 504.7 mg Cefalexin-Benzathin)

Sonstige Bestandteile :

Aluminiumstearat, festes Paraffin, flüssiges Paraffin.

4.

ANWENDUNGSGEBIET(E)

Therapie und Prophylaxe aller durch Cefalexin empfindliche Staphylococcus aureus, Staphylococcus

spp. und Streptococcus spp. verursachten Euterentzündungen in der Trockenperiode.

5.

GEGENANZEIGEN

Nicht bei Tieren mit bekannter Überempfindlichkeit gegenüber Cephalosporinen anwenden. Gefahr

der Kreuzsensibilität mit Penicillinen.

6.

NEBENWIRKUNGEN

Es kann eine vorübergehende lokale Reizung erscheinen.

Falls Sie Nebenwirkungen insbesondere solche, die nicht in der Packungsbeilage aufgeführt sind, bei

Ihrem Tier feststellen, teilen Sie diese Ihrem Tierarzt oder Apotheker mit.

7.

ZIELTIERART(EN)

Rind

8.

DOSIERUNG FÜR JEDE TIERART, ART UND DAUER DER ANWENDUNG

Das Euter vor der Applikation vollständig ausmelken. Zitze und Zitzenöffnung sind mit dem

beigelegten Reinigungstuch gründlich zu reinigen und zu desinfizieren. Für jede Zitze ein anderes

Reinigungstuch verwenden. Es ist darauf zu achten, dass die Injektorspitze nicht mit den Fingern

berührt und kontaminiert wird. In jedes Viertel den Inhalt eines Injektors vorsichtig injizieren.

Das Produkt durch leichte Massage der Zitze und des Euters verteilen.

9.

HINWEISE FÜR DIE RICHTIGE ANWENDUNG

Zur Vermeidung der Kontaminierung der Milchdrüse durch auf dem Euter vorhandene Bakterien

sollten die oben aufgeführten Vorsichtsmassnahmen für die Anwendung bei Tieren genau beachtet

werden.

10.

WARTEZEIT

Milch: 0 Tage.

Die Wartezeit von 0 Tagen ist nur dann gültig, wenn die Behandlung während der Trockenstehzeit,

welche mindestens 2 Monate vor dem Abkalben stattfinden soll, durchgeführt wurde.

Essbares Gewebe: 4 Tage.

11.

BESONDERE LAGERUNGSHINWEISE

In der Originalverpackung und nicht über 25°C lagern

Arzneimittel unzugänglich für Kinder aufbewahren.

12.

BESONDERE WARNHINWEISE

Besondere Vorsichtsmaßnahmen für die Anwendung bei Tieren

Zur Vermeidung der Kontaminierung der Milchdrüse durch auf dem Euter vorhandene Bakterien

sollten die oben aufgeführten Vorsichtsmassnahmen für die Anwendung bei Tieren genau beachtet

werden.

Besondere Vorsichtsmaßnahmen für den Anwender

Penicilline und Cephalosporine können nach Injektion, Einnahme, Aufnahme oder Hautkontakt

Überempfindlichkeitsreaktionen (Allergien) hervorrufen. Überempfindlichkeitsreaktionen gegenüber

Penicilline und Cephalosporine können sich kreuzen. Allergische Reaktionen gegenüber dieser

Substanzen können ernsthaft sein.

Bei bekannter Überempfindlichkeit oder wenn vom Umgang mit derartigen Präparaten abgeraten

wurde, Produkt nicht handhaben.

Um möglichem Kontakt zu vermeiden, Produkt mit großer Sorgfalt handhaben.

Bei Haut- und Augenkontakt mit dem Tierarzneimittel sofort mit Wasser abspülen.

Sollten nach dem Kontakt mit dem Tierarzneimittel Symptome wie Hautausschlag auftreten, ist

ärztlicher Rat einzuholen und diese Gebrauchsinformation vorzulegen.

Schwellungen im

Gesicht, der Lippen oder Augen oder Probleme bei der Atmung sind ernsthafte

Symptome, die einer sofortigen medizinischen Behandlung bedürfen.

Nach der Anwendung Hände waschen.

Anwendung während der Trächtigkeit, Laktation oder der Legeperiode

Nicht innerhalb von zwei Monaten vor dem Abkalben anwenden.

Nicht während der Laktation anwenden.

13.

BESONDERE VORSICHTSMASSNAHMEN FÜR DIE ENTSORGUNG VON NICHT

VERWENDETEM ARZNEIMITTEL ODER VON ABFALLMATERIALIEN, SOFERN

ERFORDERLICH

Nicht verwendete Tierarzneimittel oder davon stammende Abfallmaterialien sind entsprechend den

örtlichen Vorschriften zu entsorgen.

14.

GENEHMIGUNGSDATUM DER PACKUNGSBEILAGE

Januar 2016

15.

WEITERE ANGABEN

Es werden möglicherweise nicht alle Packungsgrößen in Verkehr gebracht.

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