Program 80 ad us. vet.

Hauptinformation

  • Handelsname:
  • Program® 80 ad us. vet., Injektionssuspension für Katzen
  • Darreichungsform:
  • Injektionssuspension für Katzen
  • 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:
  • Program® 80 ad us. vet., Injektionssuspension für Katzen
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • 10%ige Injektionssuspension zur Flohbekämpfung bei Katzen.

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 54239
  • Letzte Änderung:
  • 02-09-2017

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

Program

80 ad us. vet., Injektionssuspension für Katzen

Elanco Tiergesundheit AG

10%ige Injektionssuspension zur Flohbekämpfung bei Katzen.

ATCvet: QP53BC01

Zusammensetzung

Program Injektionssuspension mit 10% (w/w) Lufenuron (INN):

Program 80 enthält 80 mg Lufenuron pro vorgefüllte Spritze (0.8 ml Injektionssuspension).

Hilfsstoffe: Polysorbat 21 (Tensid), Kollidon 12PF (Dispersionsmittel), Natrii chloridum,

Aqua ad injectabilia q.s. ad suspensionem pro vase.

Fachinformationen Wirkstoffe (CliniPharm)

Lufenuron

Eigenschaften / Wirkungen

Program enthält Lufenuron, ein Benzoyl-Harnstoff-Derivat. Lufenuron ist ein Insekten-

Entwicklungshemmer, der die Chitinsynthese hemmt. Der Wirkstoff wird von den Flöhen

mit dem Blut aufgenommen und gelangt in die Floheier. Die für Insekten charakteristische

Bildung larvaler Chitinstrukturen wird blockiert, und die Entwicklung der zahlreichen

Nachkommen dadurch verhindert. Damit unterbleibt der oft schubweise Neubefall der

Katze durch Flöhe. Flöhe, die die Katze ausserhalb des Hauses befallen, können keine

Neuinfestation im Hause verursachen.

Setzt die Behandlung erst nach erfolgtem Flohbefall ein, werden nach der erstmaligen

Verabreichung bis zu 3 Wochen lang noch lebensfähige Eier abgesetzt. Bei starkem

Flohbefall vor der erstmaligen Verabreichung ist deshalb eine Behandlung der Katze

gegen adulte Flöhe (z.B. mit Capstar

) zu empfehlen. Die Folgebehandlung nach

6 Monaten ist jedoch sofort wirksam.

Program reduziert bestehende, durch Flohbefall ausgelöste Hautallergien. Bei einer

diagnostizierten, hochgradigen Allergie ist eine verlängerte Behandlung mit einem

handelsüblichen Adultizid angezeigt.

Pharmakokinetik

Nach subkutaner Verabreichung wird Lufenuron relativ langsam, aber vollständig

resorbiert. Die Wirksubstanz wird im Fettgewebe eingelagert und von dort kontinuierlich in

wirksamer Dosis ans Blut abgegeben. Das Gleichgewicht der Lufenuron-Konzentrationen

in Blut und Fettgewebe garantiert die minimale effektive Konzentration von Lufenuron im

Blut während mindestens 6 Monaten. Mehr als 95% des Wirkstoffes im Blut ist an

Plasmaproteine gebunden. Lufenuron wird mehrheitlich über die Leber in unveränderter

Form mit dem Kot ausgeschieden.

Indikationen

Zur Flohbekämpfung bei Katzen.

Dosierung / Anwendung

Die empfohlene Mindestdosierung von Program Injektionssuspension für Katzen beträgt

10 mg pro kg Körpergewicht.

Program 40: Inhalt einer Spritze alle 6 Monate für Katzen und entwöhnte Kätzchen bis zu

4 kg Körpergewicht.

Program 80: Inhalt einer Spritze alle 6 Monate für Katzen ab 4 kg Körpergewicht.

Für einen anhaltenden Schutz vor Flohbefall wird empfohlen, Katzen alle 6 Monate mit

Program Injektionssuspension zu behandeln. Program kann vorzugsweise vorbeugend vor

Beginn der Flohsaison (beginnend je nach Klima etwa März bis Mai) aber auch nach

erfolgter Diagnose eines Flohbefalls eingesetzt werden.

Zur subkutanen Injektion. Die vorgefüllte Spritze vor der Injektion kräftig schütteln, damit

eine homogene Suspension gesichert ist. Damit die volle Wirkung des Produktes erreicht

wird, muss der ganze Inhalt einer vorgefüllten Spritze injiziert werden. Es wird empfohlen,

dorsal hinter den Schulterblättern zu injizieren.

Es ist wichtig, dass alle Katzen und Hunde, die in einem Haushalt zusammenleben, mit

Program behandelt werden.

Für Hunde sind Program Tabletten zu verwenden.

Anwendungseinschränkungen

a) Kontraindikationen: Keine bekannt.

b) Vorsichtsmassnahmen: Wie bei allen Iniectabilia soll die Injektionsstelle desinfiziert

werden.

Program Injektionssuspension kann bei Katzen jeden Alters und jeder Rasse angewendet

werden. Program Injektionssuspension kann auch an trächtige und laktierende Kätzinnen

verabreicht werden.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Keine bekannt. Wie andere Injektionssuspensionen (z.B. Antibiotika, Impfstoffe) kann

Program Injektionssuspension eine vorübergehende, leichte und schmerzlose Schwellung

an der Injektionsstelle verursachen.

Wechselwirkungen

Keine bekannt. Program kann mit allen handelsüblichen Produkten zur Flohbekämpfung

kombiniert werden.

Sonstige Hinweise

Bei Raumtemperatur (15 - 25°C) aufbewahren. Vor Frost schützen, nicht einfrieren. Das

Medikament darf nur bis zu dem auf der Packung mit EXP bezeichneten Datum verwendet

werden. Gebrauchte Spritzen und Nadeln als Abfall fachgerecht entsorgen. Gebrauchte

Spritzen für keine andere Anwendung einsetzen. Program Injektionssuspension ist für

Kinder unerreichbar aufzubewahren.

Packungen

Schachtel mit 10 vorgefüllten Spritzen mit 80 mg Lufenuron (0.8 ml Suspension).

Abgabekategorie: B

Swissmedic Nr. 54'239

Informationsstand: 06/2006

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Versican Plus DHPPi/L4R ad us. vet.

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Institut für Veterinärpharmakologie und toxikologie

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Activyl TickPlus spot-on Hund S ad us. vet., insektizide Loesung zum Auftragen auf die Haut

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Institut für Veterinärpharmakologie und toxikologie

12-12-2018

Activyl TickPlus spot-on Hund M ad us. vet., insektizide Loesung zum Auftragen auf die Haut

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Institut für Veterinärpharmakologie und toxikologie

12-12-2018

Activyl TickPlus spot-on Hund L ad us. vet., insektiztide Loesung zum Auftragen auf die Haut

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Institut für Veterinärpharmakologie und toxikologie

12-12-2018

Activyl TickPlus spot-on Hund XL ad us. vet., insektizide Loesung zum Auftragen auf die Haut

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Institut für Veterinärpharmakologie und toxikologie

12-12-2018

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Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 5 mg ad us. vet., Kautabletten fuer Hunde

Simparica 5 mg ad us. vet., Kautabletten fuer Hunde

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Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 10 mg ad us. vet., Kautabletten fuer Hunde

Simparica 10 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 20 mg ad us. vet., Kautabletten fuer Hunde

Simparica 20 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 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

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Institut für Veterinärpharmakologie und toxikologie

10-12-2018

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8-12-2018

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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

4-12-2018

Mylan Expands Its Voluntary Nationwide Recall of Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide Tablets, USP, to all Lots Within Expiry Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylam

Mylan Expands Its Voluntary Nationwide Recall of Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide Tablets, USP, to all Lots Within Expiry Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylam

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FDA - U.S. Food and Drug Administration

4-12-2018

Arnica compositum ad us. vet., Tabletten

Arnica compositum ad us. vet., Tabletten

● Die Neuzulassung erfolgte am 04.12.2018.

Institut für Veterinärpharmakologie und toxikologie

15-1-2019

Symbicort® Turbohaler® 80/4,5 µg

Rote - Liste

11-1-2019

Consultation: Good Clinical Practice Inspections Program

Consultation: Good Clinical Practice Inspections Program

The TGA is seeking comments from interested parties on a pilot Good Clinical Practice (GCP) Inspections Program of 12 months duration that will inform a routine GCP Inspections Program. Closing date: 22 February 2019

Therapeutic Goods Administration - Australia

21-12-2018

Binko® 80 mg Filmtabletten

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

20-12-2018


Programme to rationalise international good-manufacturing-practice inspections of active-pharmaceutical-ingredient / active-substance manufacturers: Terms of reference and procedures for participating authorities

Programme to rationalise international good-manufacturing-practice inspections of active-pharmaceutical-ingredient / active-substance manufacturers: Terms of reference and procedures for participating authorities

Programme to rationalise international good-manufacturing-practice inspections of active-pharmaceutical-ingredient / active-substance manufacturers: Terms of reference and procedures for participating authorities

Europe - EMA - European Medicines Agency

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

The Breakthrough Devices Program’s goal is to provide patients and health care providers with timely access to devices that treat or diagnose a life-threatening or irreversibly debilitating condition.

The Breakthrough Devices Program’s goal is to provide patients and health care providers with timely access to devices that treat or diagnose a life-threatening or irreversibly debilitating condition.

The Breakthrough Devices Program’s goal is to provide patients and health care providers with timely access to devices that treat or diagnose a life-threatening or irreversibly debilitating condition.

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

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


Committee for Advanced Therapies (CAT) work programme 2019

Committee for Advanced Therapies (CAT) work programme 2019

Committee for Advanced Therapies (CAT) work programme 2019

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

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