Clamoxyl 40 mg ad us. vet.[E]

Hauptinformation

  • Handelsname:
  • Clamoxyl 40 mg ad us. vet.[E], 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:
  • Clamoxyl 40 mg ad us. vet.[E], Tabletten
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Tabletten für Hund und Katze gegen bakterielle Infektionen.

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 46389
  • Letzte Änderung:
  • 02-09-2017

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

Clamoxyl 40 mg ad us. vet.

, Tabletten

Zoetis Schweiz GmbH

HINWEIS: Exportspezialität (Nur für den Vertrieb im Ausland zugelassen)!

Tabletten für Hund und Katze gegen bakterielle Infektionen.

ATCvet: QJ01CA04

Zusammensetzung

1 Tablette enthält:

Amoxicillinum anhydricum 40 mg

Excip. pro compr.

Fachinformationen Wirkstoffe (CliniPharm)

Amoxicillin

Eigenschaften / Wirkungen

Amoxicillin ist ein von Beecham aus dem Penicillinkern entwickeltes halbsynthetisches

Penicillin. Seine Eigenschaften sind:

Breites Wirkungsspektrum gegenüber einer Vielzahl von gramnegativen und

grampositiven Bakterien.

-Rasche bakterizide Wirkung.

Hervorragende Resorption nach peroraler Verabreichung und schnelle Bildung hoher

Serumtiter.

-Resorption wird durch Futteraufnahme kaum beeinträchtigt.

Rasche therapeutische Wirkung gegenüber einem breiten Spektrum bakterieller

Infektionen.

-Sehr schwache Toxizität.

-Hohe Konzentrationen in Galle und Urin.

Clamoxyl wirkt schnell bakterizid gegenüber einem breiten Spektrum von gramnegativen

und grampositiven bakteriellen Krankheitserregern, die bei Kleintieren auftreten:

Bordetella spp., Brucella spp., Clostridia spp., Corynebacterium spp., Escherichia coli,

Fusiformis spp., Haemophilus spp., Klebsiella spp., Moraxella spp., Pasteurella spp.,

Proteus mirabilis, Salmonella spp., Spirochaeten, einschliesslich Leptospira spp.,

Staphylokokken (Penicillinasebildner ausgenommen), Streptokokken und Vibrio spp.

Indikationen

Behandlung von Infektionen, die durch Amoxicillin-empfindliche Keime verursacht worden

sind, bei Hund und Katze:

Lokale Indikationen: Wunden, Hautinfektionen und Abszesse, bakterielle Dermatitiden,

Otitis.

Respiratorische Infektionen: Pneumonie, Bronchitis, Tonsillitis, Rhinitis, Laryngo-

Tracheitis.

Infektionen im Urogenitalbereich: Puerperalinfektionen; Metritis; Nephritis; Zystitis und

Vaginitis.

-Infektionen des Verdauungstraktes: Cholangiohepatitis, Gastro-Enteritis.

-Sekundäre bakterielle Infektionen z.B. nach Staupe.

-Allgemeininfektionen: Gelenks- und Nabelinfektionen.

-Antibiotischer Schutz bei chirurgischen Eingriffen.

Nachbehandlung nach parenteraler Behandlung mit Clamoxyl in schweren Fällen, z.B.

bei Septikaemien.

Wichtig: Bei akuten Infektionen soll die Behandlung mit Clamoxyl

-Injektionen eingeleitet

werden.

Dosierung: Hund, Katze: 4 - 10 mg pro kg KGW zweimal täglich während zwei bis fünf

Tagen peroral verabreichen. Bei schweren oder akuten Erkrankungen kann die Dosis

erhöht und/oder in kürzeren Intervallen wiederholt werden. Für die Behandlung von

gramnegativen Infektionen und bei Jungtieren wird im allgemeinen die höhere Dosierung

empfohlen.

KGW Amoxicillin-Dosis Clamoxyl 40 mg

Clamoxyl 200 mg

(kg)

(mg)

(Anzahl Tbl. pro Beh.)(Anzahl Tbl. pro Beh.)

5 kg 20 - 50 mg

⁄ - 1 Tbl.

10 kg40 - 100 mg

1 - 2 ⁄ Tbl.

⁄ - ⁄ Tbl.

20 kg80 - 200 mg

2 - 5 Tbl.

⁄ - 1 Tbl.

30 kg120 - 300 mg

⁄ - 1 ⁄ Tbl.

40 kg160 - 400 mg

1 - 2 Tbl.

50 kg200 - 500 mg

1 - 2 ⁄ Tbl.

Verabreichung: Die Kautabletten werden ganz eingegeben. Bei schwer erkrankten Tieren

können sie zerdrückt und mit Flüssigkeit verabreicht werden.

Normalerweise tritt innerhalb von drei Tagen nach Beginn der Behandlung eine Besserung

ein. Sollte in diesem Zeitraum ein Therapieerfolg ausbleiben, ist die Diagnose zu

überprüfen und die Therapie eventuell zu ändern.

Anwendungseinschränkungen

Kontraindikationen:

Clamoxyl soll nicht an penicillinempfindliche Tiere verabreicht werden.

Clamoxyl Tabletten nicht bei Kaninchen, Chinchilla, Meerschweinchen, Hamster und

anderen sehr kleinen Pflanzenfressern einsetzen.

Nicht bei Tieren anwenden, die der Gewinnung von Lebensmitteln dienen.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Die Anwendung von Beta-Laktamantibiotika kann allergische Reaktionen auslösen.

Sonstige Hinweise

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

verwendet werden.

Bei Raumtemperatur (15 - 25°C) und vor Feuchtigkeit geschützt lagern.

Ausserhalb der Reichweite von Kindern aufbewahren.

Packungen

Nur für den Vertrieb im Ausland bestimmt.

Exportspezialität: Vertrieb in der Schweiz nicht zugelassen!

Abgabekategorie: A

Swissmedic Nr. 46'389

Informationsstand: 06/2005

Dieser Text ist behördlich genehmigt.

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10-12-2018

.@US_FDA is emphasizing the importance of manual cleaning prior to disinfection or sterilization and proper servicing of duodenoscopes. Read more:  https://go.usa.gov/xPShF  #MedicalDevice #FDApic.twitter.com/HiJbgPnsPt

.@US_FDA is emphasizing the importance of manual cleaning prior to disinfection or sterilization and proper servicing of duodenoscopes. Read more: https://go.usa.gov/xPShF  #MedicalDevice #FDApic.twitter.com/HiJbgPnsPt

. @US_FDA is emphasizing the importance of manual cleaning prior to disinfection or sterilization and proper servicing of duodenoscopes. Read more: https://go.usa.gov/xPShF  #MedicalDevice #FDA pic.twitter.com/HiJbgPnsPt

FDA - U.S. Food and Drug Administration

7-12-2018

Ferrlecit® 40 mg/Ferrlecit 62,5 mg

Rote - Liste

1-12-2018

.@US_FDA scientists have replicated an imaging clinical trial using computer methods, suggesting in silico trials hold promise for regulatory evaluation.  https://ja.ma/2rdAtre pic.twitter.com/XiTbPfEkcj

.@US_FDA scientists have replicated an imaging clinical trial using computer methods, suggesting in silico trials hold promise for regulatory evaluation. https://ja.ma/2rdAtre pic.twitter.com/XiTbPfEkcj

. @US_FDA scientists have replicated an imaging clinical trial using computer methods, suggesting in silico trials hold promise for regulatory evaluation. https://ja.ma/2rdAtre  pic.twitter.com/XiTbPfEkcj

FDA - U.S. Food and Drug Administration

30-11-2018

#FDA In Brief: @US_FDA takes steps to advance the safety and accuracy of  blood glucose monitors to empower patients with diabetes with reliable  tools to manage their health. Read more:  https://go.usa.gov/xPMyA   #MedicalDevice

#FDA In Brief: @US_FDA takes steps to advance the safety and accuracy of blood glucose monitors to empower patients with diabetes with reliable tools to manage their health. Read more: https://go.usa.gov/xPMyA  #MedicalDevice

#FDA In Brief: @US_FDA takes steps to advance the safety and accuracy of blood glucose monitors to empower patients with diabetes with reliable tools to manage their health. Read more: https://go.usa.gov/xPMyA  #MedicalDevice

FDA - U.S. Food and Drug Administration

30-11-2018

.@US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall:  https://go.usa.gov/xPMEn  #MedicalDevicepic.twitter.com/YU9Iq

.@US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn  #MedicalDevicepic.twitter.com/YU9Iq

. @US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn  #MedicalDevice pic.twitter.com/YU9Iq3Yw0b

FDA - U.S. Food and Drug Administration

30-11-2018

.@US_FDA issues class I recall, the most serious type pf recall: Zimmer  Biomet, Inc. Recalls Spinal Fusion & Long Bone Stimulators Due to Lack  of Adequate Validation and Controls to Ensure Product Cleanliness. Read  more about the recall:  https://go.us

.@US_FDA issues class I recall, the most serious type pf recall: Zimmer Biomet, Inc. Recalls Spinal Fusion & Long Bone Stimulators Due to Lack of Adequate Validation and Controls to Ensure Product Cleanliness. Read more about the recall: https://go.us

. @US_FDA issues class I recall, the most serious type pf recall: Zimmer Biomet, Inc. Recalls Spinal Fusion & Long Bone Stimulators Due to Lack of Adequate Validation and Controls to Ensure Product Cleanliness. Read more about the recall: https://go.usa.gov/xPMEK  #MedicalDevice pic.twitter.com/M55ddC98wW

FDA - U.S. Food and Drug Administration

30-11-2018

.@US_FDA has selected 8 novel medical devices as participants in #FDA’s Innovation Challenge to address the #OpioidEpidemic by preventing and treating opioid use disorder. #FDAInnovationChallenge

.@US_FDA has selected 8 novel medical devices as participants in #FDA’s Innovation Challenge to address the #OpioidEpidemic by preventing and treating opioid use disorder. #FDAInnovationChallenge

. @US_FDA has selected 8 novel medical devices as participants in #FDA’s Innovation Challenge to address the #OpioidEpidemic by preventing and treating opioid use disorder. #FDAInnovationChallenge

FDA - U.S. Food and Drug Administration

29-11-2018

Andriol Testocaps 40 mg Kapseln

Rote - Liste

27-11-2018

Paroxetin-ratiopharm 40 mg Tabletten

Rote - Liste

26-11-2018

#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

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