Cestex 12.5 mg ad us. vet.

Hauptinformation

  • Handelsname:
  • Cestex 12.5 mg ad us. vet., Filmtabletten
  • Darreichungsform:
  • Filmtabletten
  • 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:
  • Cestex 12.5 mg ad us. vet., Filmtabletten
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Bandwurmmittel für Katze und Hund

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 53487
  • Letzte Änderung:
  • 02-09-2017

Packungsbeilage

Cestex 12.5 mg ad us. vet., Filmtabletten

Zoetis Schweiz GmbH

Bandwurmmittel für Katze und Hund

ATCvet: QP52AA04

Zusammensetzung

1 Filmtablette enthält:

Epsiprantelum

12.5 mg Color: E 110 et E

Excip. pro compr.

Fachinformationen Wirkstoffe (CliniPharm)

Epsiprantel

Eigenschaften / Wirkungen

Epsiprantel ist ein Anthelminthikum, das nach einmaliger Verabreichung hoch wirksam ist

gegen die üblichen Bandwürmer von Katzen und Hunden.

Epsiprantel wirkt direkt auf Bandwürmer. Cestex eliminiert die Bandwürmer meist

vollständig (Wirksamkeit > 99%). Aufgrund des Verdauungsprozesses ist es möglich, dass

im Kot nach der Behandlung keine Bandwurmteile sichtbar sind.

Indikationen

Behandlung des Befalls mit Cestoden bei Katzen und Hunden:

-Katze: Dipylidium caninum, Taenia spp., Echinococcus multilocularis

Hund: Dipylidium caninum, Taenia spp., Echinococcus granulosus, Echinococcus

multiocularis

Dosierung / Anwendung

Katze: 2.75 mg/kg KGW.

-1 Tabl. 12.5 mg für Katzen bis 4.5 kg KGW.

-1 Tabl. 25 mg für Katzen von 4.5 bis 9 kg

KGW.

Hund: 5.5 mg/kg KGW.

-1 Tabl. 12.5 mg für Hunde bis 2.3 kg KGW.

-1 Tabl. 25 mg für Hunde bis 4.5 kg KGW.

1 Tabl. 100 mg für Hunde von 9 bis 18 kg

KGW.

Die Tabletten werden einmalig peroral verabreicht. Fasten ist weder erforderlich noch

empfohlen.

Eine Reinfestation mit Cestoden ist bei erneuter Exposition mit den Zwischenwirten der

Bandwürmer wahrscheinlich. Besonders beim Befall mit Dipylidium caninum ist darum für

ein wirksames Flohbekämpfungsprogramm zu sorgen.

Die Therapie eines gesicherten Fuchsbandwurmträgers (Echinococcus multilocularis)

sollte wegen des Infektionsrisikos für den Menschen nur unter besonderen

Sicherheitsvorkehrungen in einer Klinik vorgenommen werden. Aus Sicherheitsgründen

sollten die Hunde an zwei aufeinanderfolgenden Tagen mit Cestex behandelt werden. Die

betroffenen Räumlichkeiten sind hinterher zu reinigen und zu desinfizieren. Zur

Prophylaxe des Fuchsbandwurmes bei mausenden Hunden und Kazten wird eine

monatliche Behandlung mit Cestex empfohlen.

Anwendungseinschränkungen

Kontraindikationen

Nicht an Tiere verabreichen, die jünger als sieben Wochen oder trächtig sind.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Keine bekannt. Die 90-fache therapeutische Dosis (500 mg/kg KGW) während 14 Tagen

führte bei Hunden lediglich vereinzelt zu Erbrechen. Katzen wurden bis 36-fache

therapeutische Dosen an bis zu vier Tagen verabreicht. Vereinzelt trat kurzfristig

Erbrechen auf.

Wechselwirkungen

Keine bekannt. Epsiprantel ist kein Cholinesterase-lnhibitor. Während klinischer Studien

wurde Cestex (Epsiprantel) zusammen mit Antiphlogistika, Insektiziden und Nematoziden

verabreicht, ohne dass Wechselwirkungen auftraten.

Sonstige Hinweise

Trocken und bei Raumtemperatur (15 - 25°C) lagern.

Tierarzneimittel ausser Reichweite von Kindern aufbewahren!

Das Präparat darf nur bis zu dem auf der Packung mit "Exp" bezeichneten Datum

verwendet werden.

Packungen

100 Filmtabletten

Abgabekategorie: B

Swissmedic Nr. 53'487

Informationsstand: 05/2006

Dieser Text ist behördlich genehmigt.

20-10-2018

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Credelio 450 mg ad us. vet., Kautabletten fuer Hunde

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10-10-2018

Credelio 900 mg ad us. vet., Kautabletten fuer Hunde

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Consumer Alert: Sprout Creek Farm “Margie” Cheese Batch Recalled

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24-9-2018

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FDA Animal Drug Safety Communication: FDA Reminds Veterinarians of the Differences Between Approved and Compounded Formulas of Transdermal Mirtazapine for the Management of Weight Loss in Cats

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PET Ungezieferhalsband fuer Katzen ad us. vet.

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Acknowledgement:EFSA  wishes  to  thank  the  rapporteur  Member  State  Denmark  for  thepreparatory work on this scientific output.Suggested citation:EFSA (European Food Safety Authority), Brancato A, Brocca D, Carrasco Cabrera L,De Lentdecker C, Erdos

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Save the date & Join the @US_FDA’s Patient Engagement Advisory Committee on Nov 15th to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries. Learn more: https://go.usa.gov/xPRau  #DigitalHealth #PEAC2018 pic.twitter.com/NU61Snpxxw

FDA - U.S. Food and Drug Administration

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We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4.

 http://fema.gov/hurricane-michael-rumor-co

We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4. http://fema.gov/hurricane-michael-rumor-co

We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4. http://fema.gov/hurricane-michael-rumor-control … pic.twitter.com/T3h7ZiFUrZ

FDA - U.S. Food and Drug Administration

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26-9-2018

Today, Wednesday, September 26th 2018 at 12 pm EST is the last day that the #FDA will be soliciting site visit proposals for the 2018 Experiential Learning Program. Click the link to find more about the program & submit your application:   http://go.usa.g

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Today, Wednesday, September 26th 2018 at 12 pm EST is the last day that the #FDA will be soliciting site visit proposals for the 2018 Experiential Learning Program. Click the link to find more about the program & submit your application: http://go.usa.gov/xPrum  #MedicalDevice pic.twitter.com/Zsmq00NCdd

FDA - U.S. Food and Drug Administration

19-9-2018

Reminder: #FDA site visit proposal solicitation period for the 2018  Experiential Learning Program is currently OPEN through Wednesday,  9/26/18 @ 12 pm EST. Click the link to find more about the  program & to submit your application  https://go.usa.gov/x

Reminder: #FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, 9/26/18 @ 12 pm EST. Click the link to find more about the program & to submit your application https://go.usa.gov/x

Reminder: #FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, 9/26/18 @ 12 pm EST. Click the link to find more about the program & to submit your application https://go.usa.gov/xPrum  #MedicalDevice pic.twitter.com/FN1mNN65dD

FDA - U.S. Food and Drug Administration

19-9-2018

Memantine Mylan (Mylan S.A.S.)

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14-9-2018

Agenda:  Agenda - CAT agenda of the 12-14 September 2018 meeting

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14-9-2018

Fentanyl AWD® Matrix 12 Mikrogramm/h

Rote - Liste

12-9-2018

The FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 12 pm EST. Click the link to find more about the program & to submit your application  https://go.usa.gov/x

The FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 12 pm EST. Click the link to find more about the program & to submit your application https://go.usa.gov/x

The FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 12 pm EST. Click the link to find more about the program & to submit your application https://go.usa.gov/xPrum  #FDA #MedicalDevice pic.twitter.com/Kyo5z44Os4

FDA - U.S. Food and Drug Administration

12-9-2018

ADCETRIS (Takeda Pharma A/S)

ADCETRIS (Takeda Pharma A/S)

ADCETRIS (Active substance: Brentuximab vedotin) - Centralised - Annual renewal - Commission Decision (2018)5973 of Wed, 12 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2455/R/58

Europe -DG Health and Food Safety

11-9-2018

 Focus group meeting  on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics harmonisation, European Medicines Agency, London, UK, From: 12-Oct-2018, To: 12-Oct-2018

Focus group meeting on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics harmonisation, European Medicines Agency, London, UK, From: 12-Oct-2018, To: 12-Oct-2018

This meeting will allow a direct exchange of views between the Agency’s working party and stakeholders on its draft reflection paper on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics (SPC) harmonisation (EMA/CVMP/849775/2017). It complements the public consultation on this reflection paper ending on 31 January 2019. The reflection paper follows considerations in the report on a pilot project that aimed to develop and test non-experimental appr...

Europe - EMA - European Medicines Agency

5-9-2018

The FDA's site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 at 12 pm EST. Click the link to find more about the program and to submit your application:  https://go.u

The FDA's site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 at 12 pm EST. Click the link to find more about the program and to submit your application: https://go.u

The FDA's site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 at 12 pm EST. Click the link to find more about the program and to submit your application: https://go.usa.gov/xPcpn  #MedicalDevice

FDA - U.S. Food and Drug Administration