Program 40 ad us. vet.

Hauptinformation

  • Handelsname:
  • Program® 40 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® 40 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

Program

40 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 40 enthält 40 mg Lufenuron pro vorgefüllte Spritze (0.4 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-Ent-

wicklungshemmer, 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 40 mg Lufenuron (0.4 ml Suspension).

Abgabekategorie: B

Swissmedic Nr. 54'239

Informationsstand: 06/2006

Dieser Text ist behördlich genehmigt.

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Europe - EMA - European Medicines Agency

15-9-2018

Pankreatin 40.000 Nordmark®

Rote - Liste

13-9-2018

Oraycea 40 mg

Rote - Liste

12-9-2018

The FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 12 pm EST. Click the link to find more about the program & to submit your application  https://go.usa.gov/x

The FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 12 pm EST. Click the link to find more about the program & to submit your application https://go.usa.gov/x

The FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 12 pm EST. Click the link to find more about the program & to submit your application https://go.usa.gov/xPrum  #FDA #MedicalDevice pic.twitter.com/Kyo5z44Os4

FDA - U.S. Food and Drug Administration

6-9-2018

#FDA is launching the Quality in 510(k) Review Program Pilot to help promote efficiency and consistency in the review of certain moderate-risk medical devices. Click the link to find out more information about this new program:  https://go.usa.gov/xPxVa 

#FDA is launching the Quality in 510(k) Review Program Pilot to help promote efficiency and consistency in the review of certain moderate-risk medical devices. Click the link to find out more information about this new program: https://go.usa.gov/xPxVa 

#FDA is launching the Quality in 510(k) Review Program Pilot to help promote efficiency and consistency in the review of certain moderate-risk medical devices. Click the link to find out more information about this new program: https://go.usa.gov/xPxVa  #MedicalDevice pic.twitter.com/dOcFpbed9K

FDA - U.S. Food and Drug Administration

5-9-2018

The FDA's site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 at 12 pm EST. Click the link to find more about the program and to submit your application:  https://go.u

The FDA's site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 at 12 pm EST. Click the link to find more about the program and to submit your application: https://go.u

The FDA's site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 at 12 pm EST. Click the link to find more about the program and to submit your application: https://go.usa.gov/xPcpn  #MedicalDevice

FDA - U.S. Food and Drug Administration