Baxyl LA 200 ad us. vet.

Hauptinformation

  • Handelsname:
  • Baxyl LA 200 ad us. vet., Injektionslösung
  • Darreichungsform:
  • Injektionslösung
  • 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:
  • Baxyl LA 200 ad us. vet., Injektionslösung
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Langwirkendes Oxytetrazyklin für Rinder, Schafe und Schweine

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 61419
  • Letzte Änderung:
  • 02-09-2017

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

Baxyl LA 200 ad us. vet., Injektionslösung

ufamed AG

Langwirkendes Oxytetrazyklin für Rinder, Schafe und Schweine

ATCvet: QJ01AA06

Zusammensetzung

Oxytetracyclinum (ut Oxytetracyclinum dihydricum) 200 mg, Magnesii oxidum leve,

Dimethylacetamidum, Dinatrii edetas, Antiox.: Natrii hydroxymethansulfinas 4.0 mg, Aqua

ad inject. q.s. ad solut. pro 1 ml

Fachinformationen Wirkstoffe (CliniPharm)

Oxytetracyclin

Eigenschaften / Wirkungen

Oxytetrazyklin besitzt ein breites Wirkungsspektrum gegen grampositive und

gramnegative pathogene Bakterien, sowie auch gegen Mycoplasmen, Chlamydien und

Rickettsien. Dank seiner speziellen Formulierung besitzt Baxyl LA Injektionslösung eine

lang andauernde Wirkung.

Resistenz gegen Tetrazykline ist bei diversen Bakterien wie z.B. E. coli oder gewissen

Streptococcus spp. verbreitet. Auch bei folgenden Bakterien sind Resistenzen zu

erwarten, die häufig stammspezifisch sind: Mykobakterien spp., Proteus vulgaris,

Pseudomonas aeruginosa, Serratia spp., manche Mycoplasma spp., wie M. bovis.

Pharmakokinetik

Nach intramuskulärer Injektion treten beim Rind schon nach 2 bis 8 Stunden maximale

Serumkonzentrationen auf. Therapeutische Blutspiegel halten beim Schwein während

etwa 2 Tagen an. Der Wirkstoff kann beim Schaf und beim Rind bis 5 Tage nach der

Applikation im Blut nachgewiesen werden. Die höchsten Konzentrationen werden in den

Nieren, dem Dünndarm und der Leber erreicht. Oxytetrazyklin unterliegt einem

enterohepatischen Kreislauf. Es wird in aktiver Form vor allem über den Harn sowie über

Faeces und Milch ausgeschieden.

Die biologische Halbwertszeit ist nach intramuskulärer und subkutaner Verabreichung, bei

Neugeborenen sowie bei Niereninsuffizienz verlängert.

Indikationen

Therapie bakterieller Infektionen verursacht durch Oxytetrazyklinempfindliche

Organismen.

Rind:

Anaplasmose, Aktinobazillose, Kälberdiphteroid, Klauenfäule, unterstützende Therapie bei

Mastitis, Metritis, Pasteurellose und Pneumonien

Schaf:

Moderhinke, Mastitis, Metritis, Nabel-und Gelenksentzündungen, Pneumonien

Schwein:

Rotlauf, MMA-Syndrom, Nabel-und Gelenksentzündungen

20 mg/kg Körpergewicht (1 ml Baxyl LA 200 pro 10 kg Körpergewicht), tief intramuskulär

verabreichen. Maximales Volumen pro Injektionsstelle: Rind 20 ml; Schaf 5 ml; Schwein

10 ml.

Bei schwerwiegenden Infektionen hervorgerufen durch besonders virulente, aber

tetrazyklinempfindliche Keime ist eine Wiederholungsbehandlung nach 2 - 3 Tagen

angezeigt.

Anwendungseinschränkungen

a. Kontraindikationen

Schwere Leber- und Nierenfunktionsstörungen

Überempfindlichkeit gegen Tetrazykline

b. Vorsichtsmassnahmen

Langzeitmedikation mit hoher Dosierung während der Trächtigkeit ist zu vermeiden.

Die Anwendung im Wachstumsalter kann zu einer Braunverfärbung der Zähne führen.

Der Therapieerfolg soll kontrolliert werden und insbesondere bei Ausbleiben einer Wirkung

soll eine bakteriologische Untersuchung mit Antibiogramm angeordnet werden.

Bei Pferden, Hunden und Katzen nicht verwenden.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Intramuskuläre Verabreichungen führen - tierartlich unterschiedlich ausgeprägt - zu

lokalen Entzündungsreaktionen infolge von Gewebereizung.

Rind:

Essbare Gewebe: 31 Tage,

Milch: 10 Tage

Schwein:Essbare Gewebe: 18 Tage

Schaf:

Essbare Gewebe: 9 Tage,

Milch: 7 Tage

Wechselwirkungen

Oxytetrazykline nicht mit polyvalenten Kationen (Ca

, Mg

, Fe

2+/3+

) kombinieren. Nicht

mit anderen Arzneimitteln mischen.

Es besteht ein potentieller Antagonismus von Tetrazyklinen mit bakterizid wirksamen

Antibiotika.

Sonstige Hinweise

-Lichtgeschützt und unter 25°C lagern.

-Nicht im Kühlschrank lagern oder einfrieren.

-Aufbrauchfrist nach erster Entnahme: 28 Tage.

Nach Anbruch der Flasche kann sich die Farbe der Lösung verändern, die Wirkung bleibt

unverändert.

-Injektionslösung nicht verdünnen.

-Arzneimittel für Kinder unzugänglich aufbewahren.

-Das Präparat darf nur bis zu dem mit "Exp." bezeichneten Datum verwendet werden.

Packungen

Flasche à 100 ml

Abgabekategorie: A

Swissmedic Nr. 61'419

Informationsstand: 08/2011

Dieser Text ist behördlich genehmigt.

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Institut für Veterinärpharmakologie und toxikologie

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Institut für Veterinärpharmakologie und toxikologie

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Institut für Veterinärpharmakologie und toxikologie

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Institut für Veterinärpharmakologie und toxikologie

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Institut für Veterinärpharmakologie und toxikologie

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Simparica 20 mg ad us. vet., Kautabletten fuer Hunde

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Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 40 mg ad us. vet., Kautabletten fuer Hunde

Simparica 40 mg ad us. vet., Kautabletten fuer Hunde

● Indikationserweiterung (Demodex canis, Otodectes cynotis) ● Änderung Text "Eigenschaften / Wirkungen", "Indikationen", "Dosierung / Anwendung" und "Unerwünschte Wirkungen"

Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 80 mg ad us. vet., Kautabletten fuer Hunde

Simparica 80 mg ad us. vet., Kautabletten fuer Hunde

● Indikationserweiterung (Demodex canis, Otodectes cynotis) ● Änderung Text "Eigenschaften / Wirkungen", "Indikationen", "Dosierung / Anwendung" und "Unerwünschte Wirkungen"

Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 120 mg ad us. vet., Kautabletten fuer Hunde

Simparica 120 mg ad us. vet., Kautabletten fuer Hunde

● Indikationserweiterung (Demodex canis, Otodectes cynotis) ● Änderung Text "Eigenschaften / Wirkungen", "Indikationen", "Dosierung / Anwendung" und "Unerwünschte Wirkungen"

Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Zulvac 8 Bovis ad us. vet., Suspension zur Injektion fuer Rinder

Zulvac 8 Bovis ad us. vet., Suspension zur Injektion fuer Rinder

● Änderung Text gesamte Arzneimittelinformation

Institut für Veterinärpharmakologie und toxikologie

6-12-2018

Hyalovet 20 ad us. vet., Injektionsloesung

Hyalovet 20 ad us. vet., Injektionsloesung

● Zusätzliche Applikationsart: intravenöse Anwendung

Institut für Veterinärpharmakologie und toxikologie

6-12-2018

Milteforan 20 mg/ml ad us. vet., orale Loesung

Milteforan 20 mg/ml ad us. vet., orale Loesung

● Änderung Text "Dosierung / Anwendung" (Verschlusssystem) und "Unerwünschte Wirkungen"

Institut für Veterinärpharmakologie und toxikologie

6-12-2018

Ubroseal ad us. vet., intramammaere Suspension

Ubroseal ad us. vet., intramammaere Suspension

● Die Neuzulassung erfolgte am 06.12.2018.

Institut für Veterinärpharmakologie und toxikologie

10-1-2019

Mifegyne 200 mg Tabletten

Rote - Liste

20-12-2018

.@US_FDA provides an update on new steps to revise #Essure's post-market study to collect long-term safety information following discontinuation of its U.S. sales. Read FDA Commissioner @SGottliebFDA's statement on the new steps here:  https://go.usa.gov/

.@US_FDA provides an update on new steps to revise #Essure's post-market study to collect long-term safety information following discontinuation of its U.S. sales. Read FDA Commissioner @SGottliebFDA's statement on the new steps here: https://go.usa.gov/

. @US_FDA provides an update on new steps to revise #Essure's post-market study to collect long-term safety information following discontinuation of its U.S. sales. Read FDA Commissioner @SGottliebFDA's statement on the new steps here: https://go.usa.gov/xEaNB  #MedicalDevice

FDA - U.S. Food and Drug Administration

19-12-2018

Join us on January 17, 2019 from 1-2:30 PM EST for a webinar to help clarify the Breakthrough Devices Program final guidance for manufacturers. Find out more about the webinar:  https://go.usa.gov/xExHX  #MedicalDevice #FDApic.twitter.com/sHElqFFODy

Join us on January 17, 2019 from 1-2:30 PM EST for a webinar to help clarify the Breakthrough Devices Program final guidance for manufacturers. Find out more about the webinar: https://go.usa.gov/xExHX  #MedicalDevice #FDApic.twitter.com/sHElqFFODy

Join us on January 17, 2019 from 1-2:30 PM EST for a webinar to help clarify the Breakthrough Devices Program final guidance for manufacturers. Find out more about the webinar: https://go.usa.gov/xExHX  #MedicalDevice #FDA pic.twitter.com/sHElqFFODy

FDA - U.S. Food and Drug Administration

19-12-2018

On Dec. 18th, the @US_FDA issued the final guidance on the Breakthrough Devices Program. The guidance outlines program policies, features, and the process for manufacturers to follow when choosing to pursue the #breakthrough designation. Read more:  https

On Dec. 18th, the @US_FDA issued the final guidance on the Breakthrough Devices Program. The guidance outlines program policies, features, and the process for manufacturers to follow when choosing to pursue the #breakthrough designation. Read more: https

On Dec. 18th, the @US_FDA issued the final guidance on the Breakthrough Devices Program. The guidance outlines program policies, features, and the process for manufacturers to follow when choosing to pursue the #breakthrough designation. Read more: https://go.usa.gov/xExHq  pic.twitter.com/fAAZAQx1H5

FDA - U.S. Food and Drug Administration

19-12-2018

On 12/12/18 GE Healthcare Recalled CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA has identified this as a Class I Recall, the most serious type recall. Read more about the recall:  https://go.usa.gov/

On 12/12/18 GE Healthcare Recalled CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA has identified this as a Class I Recall, the most serious type recall. Read more about the recall: https://go.usa.gov/

On 12/12/18 GE Healthcare Recalled CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA has identified this as a Class I Recall, the most serious type recall. Read more about the recall: https://go.usa.gov/xE383  #MedicalDevice #FDA pic.twitter.com/S2EbMdmwpe

FDA - U.S. Food and Drug Administration

19-12-2018

ISOZID® comp. 100/200/300 mg N

Rote - Liste

19-12-2018

Ciprobay® 200 mg

Rote - Liste

18-12-2018

#DYK December is #SafeToysAndGiftsMonth. Check out @US_FDA's Consumer Update on how to keep kids safe with toys containing lasers:  https://go.usa.gov/xEx2r  #FDApic.twitter.com/57pZAmSb9r

#DYK December is #SafeToysAndGiftsMonth. Check out @US_FDA's Consumer Update on how to keep kids safe with toys containing lasers: https://go.usa.gov/xEx2r  #FDApic.twitter.com/57pZAmSb9r

#DYK December is #SafeToysAndGiftsMonth. Check out @US_FDA's Consumer Update on how to keep kids safe with toys containing lasers: https://go.usa.gov/xEx2r  #FDA pic.twitter.com/57pZAmSb9r

FDA - U.S. Food and Drug Administration

18-12-2018


Orphan designation: Mercaptopurine (oral suspension), Treatment of acute lymphoblastic leukaemia, 30/04/2009, Positive

Orphan designation: Mercaptopurine (oral suspension), Treatment of acute lymphoblastic leukaemia, 30/04/2009, Positive

Orphan designation: Mercaptopurine (oral suspension), Treatment of acute lymphoblastic leukaemia, 30/04/2009, Positive

Europe - EMA - European Medicines Agency

14-12-2018

GE Healthcare Recalls CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA @US has identified this as a Class I Recall, the most serious type recall. Read more about the recall here:  https://go.usa.gov/xE38

GE Healthcare Recalls CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA @US has identified this as a Class I Recall, the most serious type recall. Read more about the recall here: https://go.usa.gov/xE38

GE Healthcare Recalls CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA @US has identified this as a Class I Recall, the most serious type recall. Read more about the recall here: https://go.usa.gov/xE383  #MedicalDevice #FDA pic.twitter.com/X4IprwU8R2

FDA - U.S. Food and Drug Administration

14-12-2018

#ICYMI: @US_FDA cleared a mobile medical app to help those with #opioid use disorder stay in recovery programs. Read more about the clearance here:  https://go.usa.gov/xE3ke  #FDA #MedicalDevice

#ICYMI: @US_FDA cleared a mobile medical app to help those with #opioid use disorder stay in recovery programs. Read more about the clearance here: https://go.usa.gov/xE3ke  #FDA #MedicalDevice

#ICYMI: @US_FDA cleared a mobile medical app to help those with #opioid use disorder stay in recovery programs. Read more about the clearance here: https://go.usa.gov/xE3ke  #FDA #MedicalDevice

FDA - U.S. Food and Drug Administration

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

5-12-2018


Orphan designation: Paclitaxel (micellar), Treatment of ovarian cancer, 17/12/2006, Positive

Orphan designation: Paclitaxel (micellar), Treatment of ovarian cancer, 17/12/2006, Positive

Orphan designation: Paclitaxel (micellar), Treatment of ovarian cancer, 17/12/2006, Positive

Europe - EMA - European Medicines Agency