Chloropal mite ad us. vet.

Hauptinformation

  • Handelsname:
  • Chloropal mite ad us. vet., Suspension
  • Darreichungsform:
  • Suspension
  • 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:
  • Chloropal mite ad us. vet., Suspension
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Antibiotische Suspension für Hunde, Katzen und kleine Nager

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 49413
  • Letzte Änderung:
  • 02-09-2017

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

Chloropal mite ad us. vet., Suspension

Dr. E. Graeub AG

Antibiotische Suspension für Hunde, Katzen und kleine Nager

ATCvet: QJ01BA01

Zusammensetzung

1 ml Suspension enthält:

Chloramphenicolum (ut C. palmitas) 25 mg

Arom.: vanillinum et alia

Conserv.: E 211

Excipiens ad suspensionem

Fachinformationen Wirkstoffe (CliniPharm)

Chloramphenicol

Eigenschaften / Wirkungen

Chloropal mite/-forte enthält das bakteriostatisch wirkende Breitspektrum-Antibiotikum

Chloramphenicol als Chloramphenicol-Palmitat. Es wirkt gegen die meisten gram-positiven

und viele gram-negative Keime. Das geschmacksneutrale Chloramphenicol-Palmitat führt

zusammen mit der Aromatisierung zu einer guten Akzeptanz bei den Zieltierarten.

Pharmakokinetik

Nach hydrolytischer Spaltung wird das freie Chloramphenicol leicht resorbiert und es

kommt schnell zu wirksamen Konzentrationen in vielen Organen und Körperflüssigkeiten.

Chloramphenicol wird hauptsächlich in der Leber abgebaut; 10 - 20% des Wirkstoffes

werden unverändert im Urin ausgeschieden.

Indikationen

Therapie und Prophylaxe von primären und sekundären Infektionskrankheiten bei Hunden,

Katzen und kleinen Nagern, verursacht durch Chloramphenicol-empfindliche Erreger.

Hunde, Katzen, kleine Nager:

Richtdosierung: 30 - 50 mg/kg KGW täglich peroral.

1 Tropfen Chloropal mite/-forte enthält 1 mg bzw. 4 mg Chloramphenicol.

1 ml Chloropal mite/-forte enthält 25 mg bzw. 100 mg Chloramphenicol.

Chloropal mite

für 1 kg KGW =

30 -

50 Tropfen

für 2 kg KGW = 2,4 - 4 ml

für 5 kg KGW = 6 - 10 ml

für 10 kg KGW

12 - 20 ml

-Vor Gebrauch schütteln.

Die empfohlene Tagesdosis soll auf zwei bis drei Einzeldosen verteilt werden, um ein

Absinken der Blutkonzentration zu verhindern.

-Verabreichung der Einzeldosis vor den Mahlzeiten.

-Abmessen in ml mit beiliegender Kunststoffspritze (50 ml Flasche).

Anwendungseinschränkungen

Kontraindikationen

Überempfindlichkeit gegen Bestandteile des Präparates, Störungen der Blutbildung,

schwere Leber- und Nierenschäden.

Darf nicht bei Tieren angewendet werden, welche zur Lebensmittelgewinnung dienen!

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Chloropal mite/-forte wird allgemein gut vertragen. Gelegentlich können Fressunlust,

Erbrechen und Durchfall auftreten. Nach Verabreichung hoher Dosen oder Verabreichung

über längeren Zeitraum kann es vor allem bei Katzen zu einer Störung der Blutbildung

kommen.

Wechselwirkungen

Chloramphenicol hemmt den Metabolismus und verlängert dadurch die Wirkung von

anderen Wirkstoffen, wie z.B. Barbituraten, Ketamin und Phenytoin. Es steigert die

Toxizität von Primidon. Chloropal mite/-forte darf nicht mit bakterizid wirkenden

Antibiotika (z.B. Penicilline, Cephalosporine) kombiniert werden.

Sonstige Hinweise

Bei Raumtemperatur (15-25°C) lagern. Medikament ausser Reichweite von Kindern

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

Datum verwendet werden.

Packungen

Kunststoff-Flaschen zu 10 ml mit Tropfenzähler und 50 ml mit Tropfenzähler und

Kunststoffspritze (5 ml).

Abgabekategorie: A

Hersteller

Dr. E. Gräub AG, Bern (CH)

Swissmedic Nr. 49'413

Informationsstand: 02/2009

Dieser Text ist behördlich genehmigt.

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Europe -DG Health and Food Safety

28-2-2019

EU/3/12/997 (Sinus Regulatory Consulting EU Limited)

EU/3/12/997 (Sinus Regulatory Consulting EU Limited)

EU/3/12/997 (Active substance: N-hydroxy-4-(3-methyl-2-(S)-phenyl-butyrylamino) benzamide) - Transfer of orphan designation - Commission Decision (2019)1750 of Thu, 28 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004372

Europe -DG Health and Food Safety

28-2-2019

EU/3/12/996 (Sinus Regulatory Consulting EU Limited)

EU/3/12/996 (Sinus Regulatory Consulting EU Limited)

EU/3/12/996 (Active substance: N-hydroxy-4-(3-methyl-2-(S)-phenyl-butyrylamino) benzamide) - Transfer of orphan designation - Commission Decision (2019)1749 of Thu, 28 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004369

Europe -DG Health and Food Safety

28-2-2019

EU/3/12/993 (Sinus Regulatory Consulting EU Limited)

EU/3/12/993 (Sinus Regulatory Consulting EU Limited)

EU/3/12/993 (Active substance: N-hydroxy-4-(3-methyl-2-(S)-phenyl-butyrylamino) benzamide) - Transfer of orphan designation - Commission Decision (2019)1748 of Thu, 28 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004343

Europe -DG Health and Food Safety

28-2-2019

EU/3/14/1250 (Akcea Therapeutics Ireland Limited)

EU/3/14/1250 (Akcea Therapeutics Ireland Limited)

EU/3/14/1250 (Active substance: Phosphorothioate oligonucleotide targeted to transthyretin) - Transfer of orphan designation - Commission Decision (2019)1739 of Thu, 28 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004311

Europe -DG Health and Food Safety

28-2-2019

EU/3/19/2140 (Artemida Pharma Europe Limited)

EU/3/19/2140 (Artemida Pharma Europe Limited)

EU/3/19/2140 (Active substance: Humanised IGg1 monoclonal antibody targeting human transferrin receptor conjugated to human iduronate-2-sulfatase) - Orphan designation - Commission Decision (2019)1732 of Thu, 28 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000001793

Europe -DG Health and Food Safety

28-2-2019

EU/3/19/2137 (Enzyvant Therapeutics Ireland Limited)

EU/3/19/2137 (Enzyvant Therapeutics Ireland Limited)

EU/3/19/2137 (Active substance: Allogeneic cultured postnatal thymus-derived tissue) - Orphan designation - Commission Decision (2019)1729 of Thu, 28 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000002979

Europe -DG Health and Food Safety

28-2-2019

EU/3/19/2136 (Enzyvant Therapeutics Ireland Limited)

EU/3/19/2136 (Enzyvant Therapeutics Ireland Limited)

EU/3/19/2136 (Active substance: Allogeneic cultured postnatal thymus-derived tissue) - Orphan designation - Commission Decision (2019)1728 of Thu, 28 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000002977

Europe -DG Health and Food Safety

25-2-2019

EU/3/17/1880 (Chemocentryx Ireland Limited)

EU/3/17/1880 (Chemocentryx Ireland Limited)

EU/3/17/1880 (Active substance: Avacopan) - Transfer of orphan designation - Commission Decision (2019)1618 of Mon, 25 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004221

Europe -DG Health and Food Safety

25-2-2019

EU/3/10/732 (Southwood Research Limited)

EU/3/10/732 (Southwood Research Limited)

EU/3/10/732 (Active substance: Entinostat) - Transfer of orphan designation - Commission Decision (2019)1631 of Mon, 25 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004131

Europe -DG Health and Food Safety

25-2-2019

EU/3/15/1518 (Novartis Europharm Limited)

EU/3/15/1518 (Novartis Europharm Limited)

EU/3/15/1518 (Active substance: Adenovirus-associated viral vector serotype 2 containing the human RPE65 gene) - Transfer of orphan designation - Commission Decision (2019)1628 of Mon, 25 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000003549

Europe -DG Health and Food Safety

25-2-2019

EU/3/12/981 (Novartis Europharm Limited)

EU/3/12/981 (Novartis Europharm Limited)

EU/3/12/981 (Active substance: Adenovirus associated viral vector serotype 2 containing the human RPE65 gene) - Transfer of orphan designation - Commission Decision (2019)1627 of Mon, 25 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000003485

Europe -DG Health and Food Safety

25-2-2019

BLUEVAC BTV8 (CZ Veterinaria, S.A.)

BLUEVAC BTV8 (CZ Veterinaria, S.A.)

BLUEVAC BTV8 (Active substance: Bluetongue virus inactivated, serotype 8) - Centralised - Yearly update - Commission Decision (2019)1610 of Mon, 25 Feb 2019

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

Simbrinza (Novartis Europharm Limited)

Simbrinza (Novartis Europharm Limited)

Simbrinza (Active substance: Brinzolamide / Brimonidine tartrate) - Centralised - Renewal - Commission Decision (2019)1590 of Fri, 22 Feb 2019 European Medicines Agency (EMA) procedure number: EMEA/H/C/3698/R/14

Europe -DG Health and Food Safety