Esb3 30% ad us. vet.[E]

Hauptinformation

  • Handelsname:
  • Esb3 30% ad us. vet.[E], Arzneimittelvormischung
  • Darreichungsform:
  • Arzneimittelvormischung
  • 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:
  • Esb3 30% ad us. vet.[E], Arzneimittelvormischung
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Arzneimittelvormischung (lösliches Pulver) für Hühner

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 33634
  • Letzte Änderung:
  • 02-09-2017

Packungsbeilage

30% ad us. vet.

, Arzneimittelvormischung

Elanco Tiergesundheit AG

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

Arzneimittelvormischung (lösliches Pulver) für Hühner

ATCvet: QP51AG04

Zusammensetzung

Wirkstoff

Sulfaclozinum natricum monohydricum 300 g

Hilfsstoff:Saccharose 700 g

Excipiens ad pulverem pro 1 kg

Fachinformationen Wirkstoffe (CliniPharm)

Sulfaclozin

Eigenschaften / Wirkungen

30% wirkt rasch und weist ein breites Spektrum auf. Esb

30% wirkt bakteriostatisch

und antiprotozoisch durch eine selektive Inhibition der Folsäuresynthese. Dies bewirkt,

dass die Purin- und in der Folge die DNS- und RNS-Synthese unterbunden wird. Es greift

in den Entwicklungszyklus der Kokzidien und Bakterien ein und verhindert ihre

Weitervermehrung.

Sulfaclozin wirkt in vitro und in vivo gegen Eimeria spp., Salmonella gallinarum und

Pasteurella multocida.

Resistenzen gegen Sulfonamide sind primär Plasmid-gebunden.

Bei P. multocida, Salmonella spp. und Eimeria spp. sind Kreuzresistenzen zu anderen

Sulfonamiden beschrieben.

Sulfonamide sind nicht wirksam gegen Mykoplasmen.

30% beeinflusst weder die Futterverwertung noch die Legeleistung oder

EischaIenqualität nachteilig.

Pharmakokinetik

Nach oraler Verabreichung wird Sulfaclozin rasch absorbiert (T

4 - 8 h) und die

Steadystate Plasmakonzentration schnell erreicht (C

165 - 170 µg/ml). Auch bei

langandauernder Behandlung wird Sulfaclozin nicht akkumuliert, sondern rasch

ausgeschieden. Nur eine geringe Fraktion (< 0.2%) azetyliertes und biologisch inaktives

Sulfaclozin findet sich in Plasma und Gewebe. Die durchschnittliche Halbwertszeit liegt

zwischen 12 und 20 Stunden.

Indikationen

Hühnerkokzidiosen verursacht durch Eimeria spp. (E. acervulina, E. maxima, E. necatrix,

E. tenella, E. brunetti) in Aufzucht-, Mast-, Junghennen- und Legehennenbeständen.

Geflügeltyphus der Hühner nach Infektion mit Salmonella gallinarum.

Geflügelcholera der Hühner nach Infektion mit Pasteurella multocida.

Dosierung / Anwendung

Kokzidiosen verursacht durch Eimeria spp.:

20 - 40 g Esb

30%/100 kg KGW täglich während 3 Behandlungstagen, dies entspricht

60 - 120 mg Sulfaclozin/kg KGW und Tag. Behandlung wenn nötig nach 2 Tagen Pause

wiederholen.

In Betrieben mit periodisch auftretender Kokzidiose empfiehlt sich eine Behandlung nach

obigem Schema in der dritten und fünften Lebenswoche.

Geflügeltyphus (Salmonella gallinarum) und Geflügelcholera (Pasteurella

multocida):

20 - 40 g Esb

30%/100 kg KGW täglich während mindestens 5 Behandlungstagen, dies

entspricht 60 - 120 mg Sulfaclozin/kg KGW und Tag.

Der beiliegende Messlöffel fasst gestrichen voll ca. 10 g Esb

30%.

Anleitung zur Herstellung eines Fütterungsarzneimittels:

30% wird im Trinkwasser verabreicht; jede andere Trinkgelegenheit muss während

der Behandlungszeit ausgeschaltet werden.

Mediziertes Trinkwasser muss täglich mehrmals frisch zubereitet und unmittelbar nach

dem Auflösen von Esb

30% verabreicht werden. Die Fütterung wird unverändert

beibehalten.

Dosierungsrichtgrössen zur Herstellung eines Fütterungsarzneimittels:

Die Einmischrate von Esb

30% entsprechend dem Körpergewicht und der

Trinkwasseraufnahme kann nach folgender Formel ermittelt werden:

A × B

––––––– = g AMV pro l Wasser

C × 100

Achtung: Die Trinkwasseraufnahme kann je nach Alter und Gesundheitszustand der Tiere,

der Art des Futters und den klimatischen Bedingungen erheblich variieren.

Beispiel:

Trinkfertige Lösung bei kontinuierlicher Behandlung:

Broiler mit 800 g KGW und 160 ml täglicher Wasseraufnahme: 1 - 2 g Esb

30%/l

Trinkwasser.

Anwendungseinschränkungen

Kontraindikationen:

Darf nicht bei Legehennen angewendet werden, deren Eier für den menschlichen Verzehr

bestimmt sind.

Vorsichtsmassnahmen:

30% soll nur nach bakteriologischer Sicherung der Diagnose und

Sensitivitätsprüfung der beteiligten Erreger angewendet werden. Bei Ausbleiben einer

deutlichen Besserung ist nach 3 Tagen eine erneute Sensitivitätsprüfung oder ein

Therapiewechsel angezeigt.

Nach Beendigung der Behandlung ist die Fütterungseinrichtung in geeigneter Weise

gründlich zu reinigen, um Restmengen des eingesetzten Antibiotikums zu beseitigen.

Überdosierung vermeiden. Bei hohen Temperaturen steigt der Wasserkonsum.

Unterdosierung vermeiden. Bei kranken Tieren sinkt der Wasserkonsum.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Wachstum, Legeleistung und Schlupfrate werden durch die empfohlenen Dosierungen von

30% nicht beeinträchtigt.

Hühner: Essbare Gewebe: 20 Tage

Darf nicht bei Legehennen angewendet werden, deren Eier für den menschlichen Verzehr

bestimmt sind.

Wechselwirkungen

Keine bekannt.

Sonstige Hinweise

Lagerungshinweise:

30% für Kinder unzugänglich aufbewahren! Trocken und unterhalb von 25°C lagern.

Vor Licht schützen. Nach Anbruch die Packung wieder gut verschliessen und vor

Feuchtigkeit schützen.

Haltbarkeit nach Herstellung eines Fütterungsarzneimittels:

Trinkwasser: unmittelbar nach Beimischen verabreichen.

Anwenderhinweise:

Beim Umgang mit Esb

30% direkte Berührung mit Haut und Schleimhäuten vermeiden.

Schutzausrüstung, bestehend aus Schutzbekleidung, Handschuhen, Atemschutz und

Schutzbrille tragen.

Während der Handhabung weder rauchen, essen noch trinken.

Packungen

Faltschachtel mit 250 g, Schachtel mit 4 × 250 g (beide Packungen mit Messlöffel)

Exportspezialität: Vertrieb in der Schweiz nicht zugelassen!

Abgabekategorie: A

Swissmedic Nr. 33'634

Informationsstand: 10/2007

Dieser Text ist behördlich genehmigt.

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● Änderung Text "Sonstige Hinweise" und "Packungen"

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● Änderung Text "Sonstige Hinweise" und "Packungen"

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● Änderung Text "Anwendungseinschränkungen"

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● Änderung Text "Anwendungseinschränkungen"

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● Änderung Text "Anwendungseinschränkungen"

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● Änderung Text "Zusammensetzung", "Indikationen", "Dosierung/Anwendung", "Anwendungseinschränkungen", "Wechselwirkungen" und "Sonstige Hinweise"

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FDA - U.S. Food and Drug Administration

1-11-2018

evaluna® 30/125

Rote - Liste

30-10-2018

#DYK: Mammograms are still the best tool for breast cancer screening.  Check out @US_FDA’s information on the importance of choosing a certified mammography facility:  https://go.usa.gov/xPPpT  #MedicalDevice #BreastCancerAwarenessMonthpic.twitter.com/YaG

#DYK: Mammograms are still the best tool for breast cancer screening. Check out @US_FDA’s information on the importance of choosing a certified mammography facility: https://go.usa.gov/xPPpT  #MedicalDevice #BreastCancerAwarenessMonthpic.twitter.com/YaG

#DYK: Mammograms are still the best tool for breast cancer screening. Check out @US_FDA’s information on the importance of choosing a certified mammography facility: https://go.usa.gov/xPPpT  #MedicalDevice #BreastCancerAwarenessMonth pic.twitter.com/YaGqeGgrTH

FDA - U.S. Food and Drug Administration

30-10-2018

EU/3/14/1250 (Akcea Therapeutics UK Ltd)

EU/3/14/1250 (Akcea Therapeutics UK Ltd)

EU/3/14/1250 (Active substance: Phosphorothioate oligonucleotide targeted to transthyretin) - Transfer of orphan designation - Commission Decision (2018)7282 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/098/13/T/01

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2080 (Freeline Therapeutics Ltd)

EU/3/18/2080 (Freeline Therapeutics Ltd)

EU/3/18/2080 (Active substance: Recombinant adeno-associated viral vector serotype S3 containing codon-optimised expression cassette encoding human coagulation factor IX variant) - Orphan designation - Commission Decision (2018)7281 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/127/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2079 (Spark Therapeutics Ireland Ltd)

EU/3/18/2079 (Spark Therapeutics Ireland Ltd)

EU/3/18/2079 (Active substance: Recombinant adeno-associated viral vector containing a bioengineered capsid and a codon-optimised expression cassette to drive the expression of the SQ form of a B-domain deleted human coagulation factor VIII) - Orphan designation - Commission Decision (2018)7280 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/104/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2078 (Sellas Life Sciences Limited)

EU/3/18/2078 (Sellas Life Sciences Limited)

EU/3/18/2078 (Active substance: Peptides YMFPNAPYL, SGQAYMFPNAPYLPSCLES, RSDELVRHHNMHQRNMTKL and PGCNKRYFKLSHLQMHSRKHTG) - Orphan designation - Commission Decision (2018)7279 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/091/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2077 (Worphmed Srl)

EU/3/18/2077 (Worphmed Srl)

EU/3/18/2077 (Active substance: Melatonin) - Orphan designation - Commission Decision (2018)7278 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/077/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2076 (Orphan Europe S.A.R.L.)

EU/3/18/2076 (Orphan Europe S.A.R.L.)

EU/3/18/2076 (Active substance: Glycine, L-alanine, L-arginine, L-aspartic acid, L-cysteine, L-cystine, L-glutamic acid, L-histidine, L-lysine monohydrate, L-methionine, L-phenylalanine, L-proline, L-serine, L-threonine, L-tryptophan, L-tyrosine, taurine) - Orphan designation - Commission Decision (2018)7277 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/100/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2075 (Consorcio Centro de InvestigaciOn BiomEdica en Red M.P.)

EU/3/18/2075 (Consorcio Centro de InvestigaciOn BiomEdica en Red M.P.)

EU/3/18/2075 (Active substance: Gefitinib) - Orphan designation - Commission Decision (2018)7276 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/090/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2074 (PhaRA bvba)

EU/3/18/2074 (PhaRA bvba)

EU/3/18/2074 (Active substance: Avapritinib) - Orphan designation - Commission Decision (2018)7275 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/079/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2073 (Fondazione Telethon)

EU/3/18/2073 (Fondazione Telethon)

EU/3/18/2073 (Active substance: Autologous CD34+ haematopoietic stem and progenitor cells genetically modified with the lentiviral vector IDUA LV, encoding for the alpha-L-iduronidase cDNA) - Orphan designation - Commission Decision (2018)7274 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/113/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2071 (Loxo Oncology Limited)

EU/3/18/2071 (Loxo Oncology Limited)

EU/3/18/2071 (Active substance: 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile) - Orphan designation - Commission Decision (2018)7272 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/125/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2072 (FGK Representative Service GmbH)

EU/3/18/2072 (FGK Representative Service GmbH)

EU/3/18/2072 (Active substance: 6'-(R)-methyl-5-O-(5-amino-5,6-dideoxy-alpha-L-talofuranosyl)-paromamine sulfate) - Orphan designation - Commission Decision (2018)7273 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/102/18

Europe -DG Health and Food Safety

26-10-2018

Men can also be diagnosed with breast cancer. Check out the @US_FDA’s information regarding breast cancer in men, available treatments and counseling options:  https://go.usa.gov/xPPpx  ) #MedicalDevice #BreastCancerAwarenessMonthpic.twitter.com/aZBjgCGsB

Men can also be diagnosed with breast cancer. Check out the @US_FDA’s information regarding breast cancer in men, available treatments and counseling options: https://go.usa.gov/xPPpx  ) #MedicalDevice #BreastCancerAwarenessMonthpic.twitter.com/aZBjgCGsB

Men can also be diagnosed with breast cancer. Check out the @US_FDA’s information regarding breast cancer in men, available treatments and counseling options: https://go.usa.gov/xPPpx  ) #MedicalDevice #BreastCancerAwarenessMonth pic.twitter.com/aZBjgCGsB1

FDA - U.S. Food and Drug Administration

24-10-2018

It’s #BreastCancerAwarenessMonth and the @US_FDA is reminding patients and caregivers that thermography is not a substitute for mammograms.pic.twitter.com/XGJFHvut4x

It’s #BreastCancerAwarenessMonth and the @US_FDA is reminding patients and caregivers that thermography is not a substitute for mammograms.pic.twitter.com/XGJFHvut4x

It’s #BreastCancerAwarenessMonth and the @US_FDA is reminding patients and caregivers that thermography is not a substitute for mammograms. pic.twitter.com/XGJFHvut4x

FDA - U.S. Food and Drug Administration

21-10-2018

Whether it’s funding scientific research, examining policy approaches to vexing safety issues, or launching public education campaigns, you can be assured that this is a top commitment for us, and #FDA is fully engaged in promoting and protecting the heal

Whether it’s funding scientific research, examining policy approaches to vexing safety issues, or launching public education campaigns, you can be assured that this is a top commitment for us, and #FDA is fully engaged in promoting and protecting the heal

Whether it’s funding scientific research, examining policy approaches to vexing safety issues, or launching public education campaigns, you can be assured that this is a top commitment for us, and #FDA is fully engaged in promoting and protecting the health of the nation’s women pic.twitter.com/euQki9iqsL

FDA - U.S. Food and Drug Administration