Baytril flavour 50 mg ad us. vet.

Hauptinformation

  • Handelsname:
  • Baytril® flavour 50 mg ad us. vet., 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:
  • Baytril® flavour 50 mg ad us. vet., Tabletten
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Antibiotikum (Gyrasehemmer) für Hunde und Katzen

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 49683
  • Letzte Änderung:
  • 02-09-2017

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

Baytril

flavour 50 mg ad us. vet., Tabletten

Provet AG

Antibiotikum (Gyrasehemmer) für Hunde und Katzen

ATCvet: QJ01MA90

Zusammensetzung

1 Tablette (15 mg ohne Bruchrille, 50 mg, 150 mg und 250 mg Tablette mit Bruchrille)

enthält: 50 mg Enrofloxacin, Aromatica, Excip. pro compresso.

Fachinformationen Wirkstoffe (CliniPharm)

Enrofloxacin

Eigenschaften / Wirkungen

Enrofloxacin gehört zur chemischen Klasse der Fluorochinolone. Die Substanz besitzt eine

bakterizide Wirkung, die über eine Bindung an die A-Untereinheit der bakteriellen DNA-

Gyrase und die dadurch verursachte selektive Hemmung dieses Enzyms vermittelt wird.

Die DNA-Gyrase gehört zu den Topoisomerasen, die bei Bakterien an der Replikation,

Transkription und Rekombination der DNA beteiligt sind. Fluorochinolone beeinflussen

auch Bakterien in der Ruhephase aufgrund von Änderungen der Zellwandpermeabilität.

Diese Mechanismen erklären, warum die Lebensfähigkeit der Bakterien bei Einwirkung

von Enrofloxacin sehr schnell nachlässt. Bei Enrofloxacin liegen die inhibitorischen und die

bakteriziden Konzentrationen dicht nebeneinander. Sie sind entweder identisch oder

unterscheiden sich maximal um 1 - 2 Verdünnungsstufen.

Resistenz gegenüber Enrofloxacin kommt vor. Aufgrund des Wirkungsmechanismus

erfolgt eine Verminderung der Empfindlichkeit durch Mutationen der Gyrasegene,

Veränderung der Zellwandpermeabilität oder erhöhten Transport des Wirkstoffes aus der

Zelle. Dabei führt eine einzelne Mutation zu einer verringerten Empfindlichkeit der

Bakterien gegenüber Enrofloxacin, bis zur klinischen Resistenz sind jedoch im

allgemeinen mehrere Mutationen erforderlich (Multi-Step-Typ). Pseudomonas aeruginosa

sind in der Regel weniger empfindlich als andere Erreger und eine klinische Resistenz

kann schon nach einer Mutation auftreten (Ein-Schritt Resistenz).

Pharmakokinetik

Nach oraler Verabreichung von Enrofloxacin werden bereits 1 - 2 Stunden nach

Verabreichung maximale Wirkstoffspiegel in Serum und Geweben erreicht. Enrofloxacin

besitzt ein grosses Verteilungsvolumen. Die Konzentrationen in den Geweben und den

Organen übertreffen die Serumspiegel zumeist deutlich. Nach vorschriftsgemässer

Dosierung wird die minimale Hemmkonzentration für relevante Erreger sowohl im Plasma

als auch in verschiedenen Zielgeweben während mehrerer Stunden überschritten.

Organe, in denen hohe Konzentrationen erwartet werden können, sind beispielsweise

Lunge, Leber, Niere, Harnblase, Prostata, Gebärmutter, Haut, Knochen und lymphatisches

Gewebe.

Indikationen

Antiinfektivum zur Therapie von Infektionen, hervorgerufen durch Baytril-empfindliche

gramnegative und grampositive Bakterien. Aufgrund seines umfassenden

Wirkungsspektrums kann Baytril flavour bei bakteriellen Einzel- und Mischinfektionen

sowie Mykoplasmosen der Atmungs- und Verdauungsorgane, der Harnwege, der Haut

sowie von Wunden eingesetzt werden.

5 mg pro 1 kg Körpergewicht, das entspricht einer Tablette von:

Baytril flavour 15 mg für 3 kg KGW

Baytril flavour 50 mg für 10 kg KGW

Baytril flavour 150 mg für 30 kg KGW

Baytril flavour 250 mg für 50 kg KGW

Bei Bedarf sind auch ⁄ Tabletten zu verwenden (Ausnahme 15 mg Tablette, da keine

Bruchrille vorhanden ist).

Art und Dauer der Anwendung

Die Eingabe erfolgt direkt oder eingehüllt in Fleisch bzw. Wurst. Die Behandlung erfolgt an

5 aufeinander folgenden Tagen, bei chronischen und schwer verlaufenden Erkrankungen

an bis zu 10 Tagen. Die empfohlenen Dosierungen sollten nicht überschritten werden.

Anwendungseinschränkungen

Kontraindikationen

Nicht anwenden bei:

-Bereits bestehenden Knorpelwachstumsstörungen.

-Trächtige und laktierende Tiere sind von der Behandlung auszuschliessen.

-Tiere mit zentralen Anfallsleiden.

Vorliegen von Resistenz gegenüber Chinolonen, da gegenüber diesen eine nahezu

vollständige, gegenüber anderen Fluorochinolonen eine komplette Kreuzresistsenz

besteht.

Die Ausscheidung von Enrofloxacin erfolgt zum Teil über die Niere, bei bestehenden

Nierenschäden ist daher wie bei allen Fluorochinolonen mit einer Verzögerung der

Ausscheidung zu rechnen.

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

Vorsichtsmassnahmen

Baytril soll nur nach vorheriger bakteriologischer Sicherung der Diagnose und

Sensitivitätsprüfung der beteiligten Erreger sowie bei Vorliegen von Resistenzen

gegenüber anderen Antibiotika angewendet werden. Der Ensatz von Baytril Tabletten

sollte wie der aller Fluorochinolone aus Gründen einer möglichen Resistenzentwicklung

nicht bei Bagatellinfektionen erfolgen.

Hunde unter einem Jahr sind von der Behandlung auszuschliessen, da während der

Phase des intensiven Wachstums, artspezifisch bei grosswüchsigen Hunderassen,

Gelenkknorpelschäden auftreten können.

Aus Sicherheitsgründen wird bei sehr grossen Hunderassen wegen der längeren

Wachstumsphase ein Ausschluss bis zu 18 Monaten empfohlen.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Katzen:

Wenn bei Katzen die empfohlene Dosierung überschritten wird, kann es zu

retinotoxischen Effekten einschliesslich Erblindung kommen.

Hunde und Katzen:

-Vereinzelt gastrointestinale Störungen.

Wechselwirkungen

-Die Elimination von Theophyllin kann verzögert werden.

Bei Kombination von Baytril (Enrofloxacin) mit Chloramphenicol, Makrolid-Antibiotika oder

Tetrazyklinen können antagonistische Effekte auftreten.

Die gleichzeitige Verabreichung von magnesium- und aluminiumhaltigen Substanzen

kann die Resorption von Enrofloxacin vermindern.

Sonstige Hinweise

Nach Ablauf des Verfalldatums nicht mehr verwenden. Arzneimittel für Kinder

unzugänglich aufbewahren.

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

Lagerung bei Raumtemperatur (15 - 25°C).

Packungen

Schachtel mit 20 bzw. 200 Tabletten

Abgabekategorie: A

Hersteller

Bayer AG, D-Leverkusen

Swissmedic Nr. 49'683

Informationsstand: 12/2009

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#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

26-11-2018

Today, #FDA’s device center also posted performance report highlighting measures taken to increase predictability, transparency of 510(k) review process, incl. 50 final guidance documents on important medical device policy issues issued since 2009.  https

Today, #FDA’s device center also posted performance report highlighting measures taken to increase predictability, transparency of 510(k) review process, incl. 50 final guidance documents on important medical device policy issues issued since 2009. https

Today, #FDA’s device center also posted performance report highlighting measures taken to increase predictability, transparency of 510(k) review process, incl. 50 final guidance documents on important medical device policy issues issued since 2009. https://go.usa.gov/xPHdn 

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

21-11-2018

Amiodaron-hameln 50 mg/ml

Rote - Liste

20-11-2018

.@US_FDA issues update to safety communication warning against the use of energy-based devices to perform vaginal “rejuvenation” or vaginal cosmetic procedures. Read more:  https://go.usa.gov/xPAzk  #MedicalDevicepic.twitter.com/pv0k2yaNfj

.@US_FDA issues update to safety communication warning against the use of energy-based devices to perform vaginal “rejuvenation” or vaginal cosmetic procedures. Read more: https://go.usa.gov/xPAzk  #MedicalDevicepic.twitter.com/pv0k2yaNfj

. @US_FDA issues update to safety communication warning against the use of energy-based devices to perform vaginal “rejuvenation” or vaginal cosmetic procedures. Read more: https://go.usa.gov/xPAzk  #MedicalDevice pic.twitter.com/pv0k2yaNfj

FDA - U.S. Food and Drug Administration

20-11-2018

.@US_FDA has updated the webpage on Urogynecologic Surgical Mesh Implants. Read more:  https://go.usa.gov/xPAzD  #MedicalDevice

.@US_FDA has updated the webpage on Urogynecologic Surgical Mesh Implants. Read more: https://go.usa.gov/xPAzD  #MedicalDevice

. @US_FDA has updated the webpage on Urogynecologic Surgical Mesh Implants. Read more: https://go.usa.gov/xPAzD  #MedicalDevice

FDA - U.S. Food and Drug Administration

20-11-2018

.@US_FDA issues Class I Medical Device Recall, the most serious type of recall: Beckman Coulter Life Sciences Beckman Coulter Life Sciences recalls the FC500 Series Flow Cytometers and EPICS XL Series Flow Cytometers. Find out more:  https://go.usa.gov/xP

.@US_FDA issues Class I Medical Device Recall, the most serious type of recall: Beckman Coulter Life Sciences Beckman Coulter Life Sciences recalls the FC500 Series Flow Cytometers and EPICS XL Series Flow Cytometers. Find out more: https://go.usa.gov/xP

. @US_FDA issues Class I Medical Device Recall, the most serious type of recall: Beckman Coulter Life Sciences Beckman Coulter Life Sciences recalls the FC500 Series Flow Cytometers and EPICS XL Series Flow Cytometers. Find out more: https://go.usa.gov/xPAtn  #MedicalDevice #FDA pic.twitter.com/6e064UQ2wg

FDA - U.S. Food and Drug Administration

19-11-2018

Leponex® 50 mg

Rote - Liste

14-11-2018

The @US_FDA issues a safety communication cautioning doctors & patients of the risks associated w/ using medications that are not approved for use w/ implanted pumps that are delivered into the spinal fluid to treat or   manage pain:  https://go.usa.gov/x

The @US_FDA issues a safety communication cautioning doctors & patients of the risks associated w/ using medications that are not approved for use w/ implanted pumps that are delivered into the spinal fluid to treat or manage pain: https://go.usa.gov/x

The @US_FDA issues a safety communication cautioning doctors & patients of the risks associated w/ using medications that are not approved for use w/ implanted pumps that are delivered into the spinal fluid to treat or manage pain: https://go.usa.gov/xPfuw  #FDA #MedicalDevice pic.twitter.com/kgDSx2PQzn

FDA - U.S. Food and Drug Administration

13-11-2018

#DYK November is #DiabetesAwarenessMonth. As the number of people diagnosed with diabetes continues to grow, @US_FDA  encourages patients and caregivers to beware of illegally markets  diabetes treatments. Check out our Consumer Update on this issue  http

#DYK November is #DiabetesAwarenessMonth. As the number of people diagnosed with diabetes continues to grow, @US_FDA encourages patients and caregivers to beware of illegally markets diabetes treatments. Check out our Consumer Update on this issue http

#DYK November is #DiabetesAwarenessMonth. As the number of people diagnosed with diabetes continues to grow, @US_FDA encourages patients and caregivers to beware of illegally markets diabetes treatments. Check out our Consumer Update on this issue https://go.usa.gov/xPfDx  pic.twitter.com/OGwOusdP1w

FDA - U.S. Food and Drug Administration

8-11-2018

There's only 1 week until the 2018 Patient Engagement Advisory Committee meeting. Join the @US_FDA on Nov 15 to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries.pic.twitter.com/WkDNnXqm

There's only 1 week until the 2018 Patient Engagement Advisory Committee meeting. Join the @US_FDA on Nov 15 to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries.pic.twitter.com/WkDNnXqm

There's only 1 week until the 2018 Patient Engagement Advisory Committee meeting. Join the @US_FDA on Nov 15 to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries. pic.twitter.com/WkDNnXqmbw

FDA - U.S. Food and Drug Administration