Dolpac 25 ad us. vet.[L]

Hauptinformation

  • Handelsname:
  • Dolpac® 25 ad us. vet.[L], teilbare Tabletten
  • Darreichungsform:
  • teilbare 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:
  • Dolpac® 25 ad us. vet.[L], teilbare Tabletten
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Breitspektrumanthelmintikum für Hunde

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • Abgabekategorie
  • Letzte Änderung:
  • 03-11-2018

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

Dolpac

25 ad us. vet.

, teilbare Tabletten

Vetoquinol AG

HINWEIS: momentan nicht lieferbar (Lieferengpass)!

Breitspektrumanthelmintikum für Hunde

ATCvet: QP52AA51

Zusammensetzung

1 Tablette enthält

Praziquantelum

125.0 mg

Pyrantelum

125.0 mg

(Pyranteli pamoas)

360.0 mg

Oxantelum

500.7 mg

(Oxanteli hydrogenoembonas)1397.5 mg

Aromatica

Excip. pro compresso

Fachinformationen Wirkstoffe (CliniPharm)

Oxantel - Praziquantel - Pyrantel

Eigenschaften / Wirkungen

Dolpac enthält die drei Wirkstoffe Praziquantel, Pyrantel und Oxantel und weist damit ein

breites Wirkspektrum gegen Rund- und Bandwürmer inkl. Trichuren beim Hund auf.

Praziquantel weist eine ausgezeichnete Wirkung gegen alle beim Hund vorkommenden

Cestoden (Adulte wie Larven) auf und wirkt durch Tegumentschädigung an den vorderen

Bandwurmabschnitten. Dadurch kommt es zu einer Störung der Ca-Permeabilität und mit

der Folge einer starken Kontraktion sowie einer Dysregulation des Stoffwechsels und

letztlich zum Absterben der Parasiten.

Pyrantel wirkt durch seine lähmende Wirkung auf die Muskulatur der Würmer, durch

Aktivierung der Acetylcholin-Rezeptoren. Die Wirkung richtet sich speziell gegen Toxocara

canis, Toxascaris leonina, Ancylostoma caninum, Uncinaria stenocephala.

Oxantel ist ein m-hydroxyphenol-Derivat von Pyrantel und wirkt ausschliesslich gegen

Trichuris vulpis. Die Spezifität beruht auf unterschiedlicher Struktur der

Acetylcholinesterase.

Pharmakokinetik

Nach oraler Verabreichung wird Pyrantel rasch aber nur in geringen Mengen resorbiert

(Tmax = 1.38h, Cmax = 0.048 µg/ml) und auch rasch ausgeschieden. Praziquantel wird

ebenfalls rasch resorbiert (Tmax = 1.28 h, Cmax = 0.4 µg/ml) und auch ausgeschieden

(Halbwertzeit 1.5 h). Die Resorption von Oxantel ist unbedeutend.

Indikationen

Behandlung von Infektionen mit folgenden Rund- und Bandwürmern beim Hund:

Rundwürmer: Toxocara canis, Toxascaris leonina, Ancylostoma caninum, Uncinaria

stenocephala, Trichuris vulpis

Bandwürmer (Adulte und Larven): Echinococcus granulosus, Echinococcus multilocularis,

Dipylidium caninum, Taenia spp., Multiceps multiceps, Mesocestoides spp.

Dolpac wird einmalig in der nachfolgenden Dosierung verabreicht:

5 mg Praziquantel, 5 mg Pyrantel, 20 mg Oxantel pro kg KGW, entspricht:

Dolpac 2 1 Tablette pro 2 kg KGW

Dolpac 10

1 Tablette pro 10 kg

Dolpac 25

1 Tablette pro 25 kg

Bei diagnostiziertem Wurmbefall ist immer eine sofortige Entwurmung mit einer

Wiederholung der Behandlung nach 2 Wochen durchzuführen. Vorzugsweise sollten die

Tabletten dem Tier mit dem Futter verabreicht werden.

Prophylaktisch ist die häufige und gründliche Entfernung des Kotes, insbesondere in

Zwingern, notwendig, um die Kontamination des Bodens mit Eiern (Trichuris) zu

vermindern, und damit keine Infektionsgefahr für den Menschen besteht. Weitere

Massnahmen, um die Gefahr einer Reinfektion zu vermindern, sind die Desinfektion des

Auslaufs, Trockenlegung oder Umgraben des Bodens, sowie die Behandlung aller Hunde

in einem Zwinger.

Da insbesondere bei Befall mit Echinococcus multilocularis die Fuchsbandwurmeier auch

am Fell des Hundes kleben, empfiehlt sich zusätzlich ein Shamponieren des Hundes

(1 Tag nach Behandlung).

Der Therapieerfolg kann beispielsweise anhand koprologischer Untersuchungen zum

Nachweis von Helmintheneiern vor und nach Therapie beurteilt werden.

Anwendungseinschränkungen

Kontraindikationen: keine bekannt

Vorsichtsmassnahmen: keine notwendig

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Erbrechen und Durchfall können vereinzelt nach der Behandlung beobachtet werden.

Wechselwirkungen

Keine bekannt.

Sonstige Hinweise

Arzneimittel für Kinder unzugänglich aufbewahren.

Bei Raumtemperatur (15-25° C) lagern.

Packungen

Dolpac 25 Schachtel mit 3 und 60 teilbaren Tabletten

Abgabekategorie: B

Swissmedic Nr. 57'689

Informationsstand: 01/2010

Dieser Text ist behördlich genehmigt.

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EU/3/06/387 (Insmed Netherlands B.V.)

EU/3/06/387 (Insmed Netherlands B.V.)

EU/3/06/387 (Active substance: Amikacin sulfate (liposomal)) - Transfer of orphan designation - Commission Decision (2019)1624 of Mon, 25 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000003770

Europe -DG Health and Food Safety

25-2-2019

EU/3/14/1373 (Chemocentryx Ireland Limited)

EU/3/14/1373 (Chemocentryx Ireland Limited)

EU/3/14/1373 (Active substance: (2R,3S)-2-(4-cyclopentylaminophenyl)-1-(2-fluoro-6-methylbenzoyl)piperidine-3-carboxylic acid(4-methyl-3-trifluoromethylphenyl)amide) - Transfer of orphan designation - Commission Decision (2019)1619 of Mon, 25 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004220

Europe -DG Health and Food Safety

25-2-2019

EU/3/14/1372 (Chemocentryx Ireland Limited)

EU/3/14/1372 (Chemocentryx Ireland Limited)

EU/3/14/1372 (Active substance: (2R,3S)-2-(4-cyclopentylaminophenyl)-1-(2-fluoro-6-methylbenzoyl)piperidine-3-carboxylic acid(4-methyl-3-trifluoromethylphenyl)amide) - Transfer of orphan designation - Commission Decision (2019)1620 of Mon, 25 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004218

Europe -DG Health and Food Safety

22-2-2019


Orphan designation: Autologous CD4+ and CD8+ T cells expressing a CD19-specific chimeric antigen receptor, Treatment of follicular lymphoma, 25/05/2018, Positive

Orphan designation: Autologous CD4+ and CD8+ T cells expressing a CD19-specific chimeric antigen receptor, Treatment of follicular lymphoma, 25/05/2018, Positive

Orphan designation: Autologous CD4+ and CD8+ T cells expressing a CD19-specific chimeric antigen receptor, Treatment of follicular lymphoma, 25/05/2018, Positive

Europe - EMA - European Medicines Agency

21-2-2019


Orphan designation: Becatecarin, Treatment of cancers of the biliary tree, 25/07/2006, Withdrawn

Orphan designation: Becatecarin, Treatment of cancers of the biliary tree, 25/07/2006, Withdrawn

Orphan designation: Becatecarin, Treatment of cancers of the biliary tree, 25/07/2006, Withdrawn

Europe - EMA - European Medicines Agency

18-2-2019

Imatinib Accord (Accord Healthcare S.L.U.)

Imatinib Accord (Accord Healthcare S.L.U.)

Imatinib Accord (Active substance: Imatinib) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2019)1434 of Mon, 18 Feb 2019 European Medicines Agency (EMA) procedure number: EMEA/H/C/2681/T/25

Europe -DG Health and Food Safety

15-2-2019

Today, the @US_FDA announced an upcoming General and Plastic Surgery Devices Panel of the Medical Devices Advisory Committee Meeting that will take place on March 25-26. Learn more about the details and how to attend here:  https://go.usa.gov/xEUeu  #Medi

Today, the @US_FDA announced an upcoming General and Plastic Surgery Devices Panel of the Medical Devices Advisory Committee Meeting that will take place on March 25-26. Learn more about the details and how to attend here: https://go.usa.gov/xEUeu  #Medi

Today, the @US_FDA announced an upcoming General and Plastic Surgery Devices Panel of the Medical Devices Advisory Committee Meeting that will take place on March 25-26. Learn more about the details and how to attend here: https://go.usa.gov/xEUeu  #MedicalDevice #FDA

FDA - U.S. Food and Drug Administration

13-2-2019

Zinkorot® 25 Tabletten

Rote - Liste

7-2-2019

Equisolon (Le Vet B.V.)

Equisolon (Le Vet B.V.)

Equisolon (Active substance: Prednisolone) - Centralised - Renewal - Commission Decision (2019)936 of Thu, 07 Feb 2019 European Medicines Agency (EMA) procedure number: EMEA/V/C/2382/R/04

Europe -DG Health and Food Safety

5-2-2019

Juluca 50 mg/25 mg Filmtabletten

Rote - Liste