Kalmivet 12,5 mg

Hauptinformation

  • Handelsname:
  • Kalmivet 12,5 mg Tablette
  • Dosierung:
  • 12,5 mg
  • Darreichungsform:
  • Tablette
  • 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:
  • Kalmivet 12,5 mg Tablette
    Belgien
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Phenothiazine

Weitere Informationen

Status

  • Quelle:
  • AFMPS - Agence Fédérale des Médicaments et des Produits de Santé - Belgium
  • Zulassungsnummer:
  • BE-V188684
  • Letzte Änderung:
  • 17-04-2018

Packungsbeilage

Bijsluiter – DE versie

Kalmivet

II. PACKUNGSBEILAGE

- 1 -

Bijsluiter – DE versie

Kalmivet

PACKUNGSBEILAGE

Kalmivet, Tabletten für Hund und Katze

1.

NAME UND ANSCHRIFT DES ZULASSUNGSINHABERS UND, WENN

UNTERSCHIEDLICH, DES HERSTELLERS, DER FÜR DIE CHARGENFREIGABE

VERANTWORTLICH IST

Zulassungsinhaber:

VETOQUINOL N.V./S.A.

Kontichsesteenweg 42

B- 2630 AARTSELAAR

Für die Chargenfreigabe verantwortlicher Hersteller:

VETOQUINOL SA

Magny-Vernois

BP 189

F- 70204 LURE Cedex

2.

BEZEICHNUNG DES TIERARZNEIMITTELS

Kalmivet, Tabletten für Hund und Katze

Acepromazinmaleat

3.

WIRKSTOFF(E) UND SONSTIGE BESTANDTEILE

Wirkstoff:

Pro Tablette: Acepromazinmaleat 17 mg (entsprechend Acepromazin base 12,5 mg)

4.

ANWENDUNGSGEBIET(E)

Beruhigungsmittel für Hunde und Katzen, um den bei ungewöhnlichen Situationen hervorgerufenen

Stress zu vermindern: tierärztliche Untersuchung, Transport.

Antiemetikum (bei Reisenkrankheit, vor einem Eingriff).

Narkose-Prämedikation.

5.

GEGENANZEIGEN

- hypovolämische Hypotension

- Herz-, Leber- und Niereninsuffizienz

- Läppchenproben (Hemmung der H1 Histaminrezeptoren)

- Phenothiazinallergie

- Epilepsie

Acepromazin vermindert nicht den Schmerz.

6.

NEBENWIRKUNGEN

Die häufigste Nebenwirkung ist die von einer reflexartigen Tachykardie eventuell begleitete

Hypotonie.

Auch können Hypothermie, Hyperglykämie, Aufregung, Regurgitation auftreten.

- 2 -

Bijsluiter – DE versie

Kalmivet

Seltener Hemmung der Blutplättchenfunktion und Thrombozytopenie.

Vor allem bei Hunden kann es zu einem Vorfall des dritten Augenlides kommen.

Bei höherer Dosierung werden selten extrapyramidale Symptome (Steifheit, Zittern) beobachtet.

Falls Sie eine Nebenwirkung bei Ihrem Tier/Ihren Tieren feststellen, die nicht in der Packungsbeilage

aufgeführt ist, teilen Sie diese Ihrem Tierarzt oder Apotheker mit.

7.

ZIELTIERART(EN)

Hunde und Katzen

8.

DOSIERUNG FÜR JEDE TIERART, ART UND DAUER DER ANWENDUNG

Je nach dem Grad und der Dauer der gewünschten Beruhigung:

Hunde: 1,25 bis 5 mg Acepromazin pro Kg Körpergewicht

(= 1 bis 4 Tabletten Kalmivet pro 10 Kg Körpergewicht)

Katzen: 2,5 mg Acepromazin pro Kg Körpergewicht

(= 1 Tablette Kalmivet pro 5 Kg Körpergewicht)

Orale Anwendung

9.

HINWEISE FÜR DIE RICHTIGE ANWENDUNG

Die Dosis wird 1 Stunde vor dem Transport oder jeder anderen Stresssituation verabreicht. Es kann

notwendig sein, die Verabreichung 3 bis 6 Stunden nach der letzten Einnahme zu wiederholen.

Wenn nötig, in etwas Nahrung einhüllen.

10.

WARTEZEIT

Entfällt

11.

BESONDERE LAGERUNGSHINWEISE

Unter 25°C lagern. Nicht einfrieren.

Arzneimittel unzugänglich für von Kinder aufbewahren.

12.

BESONDERE WARNHINWEISE

Besondere Vorsichtsmassnahmen für jede Zieltierart

Vorsichtig anwenden bei geschwächten, schwachen oder älteren Tieren sowie Tieren mit einer

Herzinsuffizienz.

Besondere Vorsichtsmassnahmen

Besondere Vorsichtsmassnahmen für die Anwendung bei Tieren

Beim Einsatz als Antiemetikum muss eine Intoxikation als auslösende Ursache für das

Erbrechen ausgeschlossen werden.

Besondere Vorsichtsmasnahmen für den Anwender

Keine

- 3 -

Bijsluiter – DE versie

Kalmivet

Anwendung während der Trächtigkeit, Laktation oder der Legeperiode

Aufgrund fehlender Ergebnisse zur Wirkung auf den Fötus und zum Übertritt in die Milch wird

empfohlen, die Anwendung von Kalmivet bei trächtigen oder laktierenden Tieren zu vermeiden.

Wechselwirkungen mit anderen Arzneimitteln und andere Wechselwirkungen

Die dämpfende Wirkung von Kalmivet wird durch die gleichzeitige Anwendung von anderen zentral

dämpfenden Stoffen (Morphinderivate, Barbiturate, Xylazin …) verstärkt.

Die gastrointestinale Resorption von Acepromazin kann durch die gleichzeitige Gabe von

Medikamenten gegen Durchfall und Antacida verringert werden. Aufgrund einer deutlichen

Wirkungsverstärkung nicht gleichzeitig mit Organophosphaten (Entwurmungsmittel/Insektizide) oder

Procain-HCl anwenden.

Antihypertensiva können die blutdrucksenkende Wirkung von Kalmivet verstärken.

Überdosierung (Symptome, Notfallmassnahmen, Gegenmittel)

Katzen reagieren auf eine Überdosierung sehr viel empfindlicher als Hunde.

Nach einer oralen Aufnahme von großen Mengen an Kalmivet sollte eine Magenspülung durchgeführt

werden.

Die Therapie erfolgt symptomatisch (Herz-Kreislauf-Wiederbelebung).

Im Falle einer Überdosierung mit nachfolgenden Herz-Kreislauf-Störungen ist das passende

Gegenmittel Noradrenalin (NICHT Adrenalin).

13.

BESONDERE VORSICHTSMASSNAHMEN FÜR DIE ENTSORGUNG VON NICHT

VERWENDETEM ARZNEIMITTEL ODER VON ABFALLMATERIALIEN, SOFERN

ERFORDERLICH

Nicht aufgebrauchte Tierarzneimittel sind vorzugsweise bei Schadstoffsammelstellen abzugeben.

Arzneimittel sollten nicht über das Abwasser oder den Haushaltsabfall entsorgt werden.

Fragen Sie Ihren Tierarzt, wie nicht mehr benötigte Arzneimittel zu entsorgen sind. Diese Maßnahmen

dienen dem Umweltschutz.

14.

GENEHMIGUNGSDATUM DER PACKUNGSBEILAGE

Dezember 2007

15.

WEITERE ANGABEN

Art und Beschaffenheit des Behältnisses

Schachtel mit 2 Blistern mit 10 Tabletten aus gelbem-orangem PVC-Aluminium

Schachtel mit 4 Blistern mit 10 Tabletten aus gelbem-orangem PVC-Aluminium

Es werden möglicherweise nicht alle Packungsgrößen in Verkehr gebracht.

Auslieferung

Auf veterinärmedizinische Verordnung

Zulassungsnummer

BE-V188684

- 4 -

9-5-2018

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