Caniphedrin 50 mg ad us. vet.

Hauptinformation

  • Handelsname:
  • Caniphedrin 50 mg ad us. vet., Tabletten
  • Darreichungsform:
  • Tabletten
  • 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:
  • Caniphedrin 50 mg ad us. vet., Tabletten
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Tabletten zur Behandlung der Harninkontinenz bei Hunden

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 47066
  • Letzte Änderung:
  • 02-09-2017

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

Caniphedrin 50 mg ad us. vet., Tabletten

PDF-Version:

Français

Streuli Pharma AG

Tabletten zur Behandlung der Harninkontinenz bei Hunden

ATCvet: QG04BX90

Zusammensetzung

1 Tablette enthält:

Wirkstoff: Ephedrini hydrochloridum 50 mg.

Hilfsstoffe: Excipiens pro compresso.

Fachinformationen Wirkstoffe (CliniPharm)

Ephedrin

Eigenschaften / Wirkungen

Erworbene Harninkontinenz nach der Kastration betrifft ca. 20% der kastrierten

Hündinnen.

Schwere Rassen sind davon wesentlich häufiger betroffen als leichte.

Die Ursache der Inkontinenz ist ein Nachlassen des Harnröhrenverschlussdruckes nach

der Kastration. Der Grund für dieses Nachlassen ist bis heute nicht bekannt.

Ephedrin ist ein α-adrenerger Wirkstoff, der den Harnröhrenverschluss verbessert.

Unter den verschiedenen angewendeten Therapieversuchen erweist sich heute die

Dauertherapie mit Ephedrin als eine der am meisten Erfolg versprechenden Methoden.

Indikationen

Incontinentia urinae der kastrierten Hündin sowie Harninkontinenz bei älteren Hündinnen

und Rüden, sofern eine entzündliche Genese ausgeschlossen werden kann.

1 - 2 mg pro kg Körpergewicht täglich.

Während den ersten 10 Behandlungstagen 2 mg pro kg Körpergewicht täglich.

Tritt der gewünschte Therapieerfolg ein, wird die Dosis versuchsweise auf 1 mg pro kg

Körpergewicht reduziert. Treten keine Rezidive auf, wird diese erniedrigte Dosis als

Dauertherapie beibehalten; andernfalls muss wieder auf 2 mg pro kg Körpergewicht erhöht

werden.

Anwendungseinschränkungen

Kontraindikationen:

Nicht anwenden bei Tieren mit schweren cardiovaskulären Erkrankungen, speziell

Arrhythmien.

Vorsichtsmassnahmen:

Nur unter Kontrolle verwenden bei Hunden mit Glaukom, Prostatahypertrophie,

Hyperthyreoidismus, Diabetes mellitus und Bluthochdruck.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Als Nebenwirkung kann Unruhe auftreten, Tachykardie und Bluthochdruck. Manche Tiere

leiden unter fehlender Fresslust.

Wechselwirkungen

Verstärkung der Herzwirkung durch halogenhaltige Narkotika.

Sonstige Hinweise

Bei Raumtemperatur (15 - 25°C) lagern.

Nur bis zu dem auf der Packung mit "EXP" angegebenen Datum verwenden.

Vor Kindern geschützt aufbewahren.

Packungen

Packungen zu 100 und 500 Tabletten

Abgabekategorie: B

Swissmedic Nr. 47'066

Informationsstand: 06/2008

Dieser Text ist behördlich genehmigt.

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#DYK November is #NationalHealthySkinMonth. Are you thinking about getting Dermal Fillers? Check out the @US_FDA's information on Dermal Fillers before you do:  https://go.usa.gov/xPHtk   #FDA #MedicalDevice

#DYK November is #NationalHealthySkinMonth. Are you thinking about getting Dermal Fillers? Check out the @US_FDA's information on Dermal Fillers before you do: https://go.usa.gov/xPHtk  #FDA #MedicalDevice

#DYK November is #NationalHealthySkinMonth. Are you thinking about getting Dermal Fillers? Check out the @US_FDA's information on Dermal Fillers before you do: https://go.usa.gov/xPHtk  #FDA #MedicalDevice

FDA - U.S. Food and Drug Administration

26-11-2018

Today, #FDA’s device center also posted performance report highlighting measures taken to increase predictability, transparency of 510(k) review process, incl. 50 final guidance documents on important medical device policy issues issued since 2009.  https

Today, #FDA’s device center also posted performance report highlighting measures taken to increase predictability, transparency of 510(k) review process, incl. 50 final guidance documents on important medical device policy issues issued since 2009. https

Today, #FDA’s device center also posted performance report highlighting measures taken to increase predictability, transparency of 510(k) review process, incl. 50 final guidance documents on important medical device policy issues issued since 2009. https://go.usa.gov/xPHdn 

FDA - U.S. Food and Drug Administration

23-11-2018

.@US_FDA issues Class I Medical Device Recall, the most serious type of   recall: Oscor Recalls TB Temporary Bipolar Pacing Leads Due to  Connector Separation Causing Potential for Loss of Pacing. Find out  more:  https://go.usa.gov/xPHxF  #FDA #MedicalDe

.@US_FDA issues Class I Medical Device Recall, the most serious type of recall: Oscor Recalls TB Temporary Bipolar Pacing Leads Due to Connector Separation Causing Potential for Loss of Pacing. Find out more: https://go.usa.gov/xPHxF  #FDA #MedicalDe

. @US_FDA issues Class I Medical Device Recall, the most serious type of recall: Oscor Recalls TB Temporary Bipolar Pacing Leads Due to Connector Separation Causing Potential for Loss of Pacing. Find out more: https://go.usa.gov/xPHxF  #FDA #MedicalDevice pic.twitter.com/negJ6HU4x2

FDA - U.S. Food and Drug Administration