Caniquantel pro Inj. ad us. vet.

Hauptinformation

  • Handelsname:
  • Caniquantel pro Inj. ad us. vet., Injektionslösung
  • Darreichungsform:
  • Injektionslösung
  • 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:
  • Caniquantel pro Inj. ad us. vet., Injektionslösung
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Injektionslösung zur Behandlung von Bandwurminfektionen bei Hunden und Katzen

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 54194
  • Letzte Änderung:
  • 02-09-2017

Packungsbeilage: zusammensetzung, kinische angaben, nebenwirkungen, wechselwirkungen, dosierung, schwangerschaft, stillzeit

Caniquantel pro Inj. ad us. vet., Injektionslösung

Dr. E. Graeub AG

Injektionslösung zur Behandlung von Bandwurminfektionen bei Hunden und Katzen

ATCvet: QP52AA01

Zusammensetzung

1 ml enthält:

Praziquantelum 56.8 mg

Conservans:

Chlorobutanolum hemihydricum 5 mg, Alcohol benzylicus 75 mg.

Propylenglycolum ad solutionem.

Fachinformationen Wirkstoffe (CliniPharm)

Praziquantel

Eigenschaften / Wirkungen

Praziquantel verursacht bei Bandwürmern eine Schädigung des Teguments und führt zu

Membranpermeabilitätsstörungen. Die akute Toxizität bei Mäusen, Ratten und Kaninchen

ist nach oraler, subkutaner, intraperitonealer und intramuskulärer Gabe gering. Bei

Hunden konnte die akute Toxizität wegen des emetischen Effektes nicht erreicht und

daher nicht exakt bestimmt werden. Studien zur chronischen Toxizität und Kanzerogenität

ergaben keinerlei Hinweise auf derartige Effekte. Ausserdem konnten bei

reproduktionstoxikologischen Untersuchungen keine mutagenen Effekte nachgewiesen

werden.

Pharmakokinetik

Praziquantel wird, unabhängig von der Applikationsart, rasch und vollständig resorbiert.

Die Halbwertszeit beträgt 1 - 2,5 Stunden. 80% der verabreichten Dosis werden als

Metaboliten innerhalb von 4 Tagen über die Nieren ausgeschieden.

Indikationen

Gegen alle reifen und unreifen Darmstadien von Bandwürmern bei Hunden und Katzen:

Echinococcus granulosus, Echinococcus multilocularis, Taenia hydatigena, Taenia

pisiformis, Taenia ovis, Taenia taeniaeformis (T. hydatigera), Multiceps multiceps,

Joyeuxiella pasqualei, Dipylidium caninum, Mesocestoides spp.

Caniquantel pro Inj. wird intramuskulär oder subkutan verabreicht. Die einmalige

Dosierung beträgt für Hunde und Katzen 0,1 ml/kg Körpergewicht, das entspricht 5,7 mg

Praziquantel/kg Körpergewicht. Injektionsvolumina von über 3 ml sollen bei subkutaner

Injektion auf zwei Stellen verteilt werden.

Anwendungseinschränkungen

Kontraindikationen

Keine bekannt.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Die bei schweren Hunden anzuwendenden Injektionsvolumina können bei subkutaner

Applikation zu lokalen Reizerscheinungen führen.

Wechselwirkungen

Die gleichzeitige Gabe von Dexamethason kann zur Herabseztung der

Serumkonzentration von Praziquantel führen.

Sonstige Hinweise

Nicht bei Tieren anwenden, die der Gewinnung von Lebensmitteln dienen.

Unter 30°C und vor Licht geschützt aufbewahren. Aufbrauchfrist nach 1. Entnahme:

28 Tage. Das Tierarzneimittel darf nur bis zu dem auf dem Behälter mit "EXP."

bezeichneten Datum verwendet werden. Ausser Reichweite von Kindern aufbewahren.

Packungen

Durchstechflasche zu 10 ml

Abgabekategorie: B

Swissmedic Nr. 54'194

Informationsstand: 04/2007

Dieser Text ist behördlich genehmigt.

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Silodosin Recordati (Recordati Ireland Ltd)

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Scientific recommendation on classification of advanced therapy medicinal products: In vitro cultured autologous mesenchymal stem cells isolated from bone marrow

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7-1-2019


Scientific recommendation on classification of advanced therapy medicinal products: Recombinant adeno-associated virus serotype 9 vector encoding the soluble lysosomal enzyme TPP1

Scientific recommendation on classification of advanced therapy medicinal products: Recombinant adeno-associated virus serotype 9 vector encoding the soluble lysosomal enzyme TPP1

Scientific recommendation on classification of advanced therapy medicinal products: Recombinant adeno-associated virus serotype 9 vector encoding the soluble lysosomal enzyme TPP1

Europe - EMA - European Medicines Agency

7-1-2019


Contact details of national competent authorities for requests to use a sticker to place the Unique Identifier on the outer/immediate packaging of centrally approved products

Contact details of national competent authorities for requests to use a sticker to place the Unique Identifier on the outer/immediate packaging of centrally approved products

Contact details of national competent authorities for requests to use a sticker to place the Unique Identifier on the outer/immediate packaging of centrally approved products

Europe - EMA - European Medicines Agency

7-1-2019

Consultation: Changes to a number of definitions and the scope of the medical device regulatory framework in Australia

Consultation: Changes to a number of definitions and the scope of the medical device regulatory framework in Australia

The TGA is seeking your comments on the proposal to introduce new and amended definitions, and a revised scope of the products regulated as medical devices in Australia. Closing date: 18 February 2019

Therapeutic Goods Administration - Australia