Program ad us. vet.

Hauptinformation

  • Handelsname:
  • Program® ad us. vet., für Katzen von 4,5 bis 9 kg
  • Darreichungsform:
  • für Katzen von 4,5 bis 9 kg
  • 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® ad us. vet., für Katzen von 4,5 bis 9 kg
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • 7%ige Suspension zur Kontrolle und Vorbeugung des Flohbefalls bei Katzen

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 51905
  • Letzte Änderung:
  • 02-09-2017

Packungsbeilage

Program

ad us. vet., für Katzen von 4,5 bis 9 kg

Elanco Tiergesundheit AG

7%ige Suspension zur Kontrolle und Vorbeugung des Flohbefalls bei Katzen

ATCvet: QP53BC01

Zusammensetzung

Program-Suspension 266 mg für Katzen von 4,5 bis 9 kg enthält 266 mg Lufenuron (INN)

pro Ampulle (3,8 g Suspension), Conserv. E 216, E 218.

Fachinformationen Wirkstoffe (CliniPharm)

Lufenuron

Eigenschaften / Wirkungen

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

wicklungshemmer, der die Chitinbildung hemmt. Der Wirkstoff wird von den Flöhen mit

dem Blut aufgenommen und gelangt in die Floheier. Die Entwicklung der Flohlarven wird

dadurch verhindert. Damit unterbleibt der oft schubweise Neubefall der Katze durch Flöhe.

Setzt die Behandlung erst nach erfolgtem Flohbefall ein, werden schon 24 Stunden nach

der ersten Dosierung keine entwicklungsfähigen Floheier mehr abgesetzt. Die

Verminderung des Flohbefalls auf dem Tier wird, je nach Verseuchung der Umgebung mit

Eiern, Larven und Puppen und den klimatischen Bedingungen (Luftfeuchtigkeit und

Temperatur), im Verlauf der folgenden Behandlungen eintreten. Bei starkem Flohbefall ist

zusätzlich eine sofortige Behandlung der Katze gegen Flöhe angezeigt.

Program verhindert die Entwicklung der Floharten Ctenocephalides felis und C. canis.

Pharmakokinetik

Nach Verabreichung von Program wird rund die Hälfte des Wirkstoffes rasch aus dem

Darm aufgenommen und gelangt innerhalb von 48 bis 72 Stunden nach Verabreichung in

das Fettgewebe. Von dort wird Lufenuron fortlaufend in kleiner, wirksamer Dosis ans Blut

abgegeben. Durch dieses Gleichgewicht Blut/Fettgewebe wird die minimale wirksame

Konzentration während mindestens 30 Tagen aufrechterhalten. Ein genügend hoher Anteil

des Wirkstoffes wird nur bei Verabreichung auf vollen Magen vom Körper aufgenommen.

Das heisst, dass die Suspension mit oder unmittelbar nach einer vollen Mahlzeit (in einem

Leckerbissen versteckt) oder durch direkte Eingabe verabreicht werden soll. Der nicht aus

dem Darm aufgenommene Anteil an Wirkstoff wird ohne im Stoffwechsel abgebaut zu

werden mit dem Kot wieder ausgeschieden.

Indikationen

Kontrolle und Vorbeugung des Flohbefalls bei Katzen.

Dosierung / Anwendung

Die Dosierung von Program bei Katzen beträgt monatlich 30 mg Lufenuron pro kg

Körpergewicht.

Praktische Dosierungsanleitung:

Katzen von 1 bis 4.5 kg KGW:

Inhalt einer Ampulle Program Suspension 133 mg pro Monat

Katzen über 4.5 kg KGW:

Inhalt einer Ampulle Program Suspension 266 mg pro Monat

Program kann vorbeugend vor Beginn der Flohsaison (beginnend je nach Klima etwa

März bis Mai) oder nach erfolgter Diagnose eines Flohbefalls eingesetzt werden. Program

soll während mindestens sechs Monaten verabreicht werden.

Program-Suspension soll mit oder unmittelbar nach einer vollen Mahlzeit (in einem

Leckerbissen versteckt) oder durch direkte Eingabe verabreicht werden.

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

Kontraindikationen

Keine bekannt

Vorsichtsmassnahmen

Keine. Program kann auch an trächtige Katzen und entwöhnte Jungkatzen ab 1 kg

verabreicht werden.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Keine bekannt.

Wechselwirkungen

Keine bekannt. Program kann mit allen handelsüblichen Produkten zur Flohbekämpfung

verwendet werden.

Sonstige Hinweise

Program Suspension ist für Kinder unerreichbar aufzubewahren. Nicht über 30°C lagern.

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

verwendet werden.

Packungen

Schachteln mit 6 Ampullen.

Abgabekategorie: D

Swissmedic Nr. 51'905

Informationsstand: 08/2002

Dieser Text ist behördlich genehmigt.

9-10-2018

Metacam 5 mg/ml ad us. vet., Injektionsloesung

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Institut für Veterinärpharmakologie und toxikologie

2-10-2018

Forthyron 200 ad us. vet., Tabletten

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● Die Zulassung ist am 02.10.2018 erloschen.

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2-10-2018

Forthyron 400 ad us. vet., Tabletten

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● Die Zulassung ist am 02.10.2018 erloschen.

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1-10-2018

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26-9-2018

Gleptosil ad us. vet., Injektionsloesung

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Institut für Veterinärpharmakologie und toxikologie

21-9-2018

FDA Animal Drug Safety Communication: FDA Reminds Veterinarians of the Differences Between Approved and Compounded Formulas of Transdermal Mirtazapine for the Management of Weight Loss in Cats

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20-9-2018

Siu & Sons Int'l Trading recalls Color Fantastik Assorted Rubber Animal Toys

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20-9-2018

Drontal Plus Tasty ad us. vet., Tabletten fuer Hunde

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Institut für Veterinärpharmakologie und toxikologie

20-9-2018

Euthoxin 500 mg/ml ad us. vet., Injektionsloesung

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Institut für Veterinärpharmakologie und toxikologie

19-9-2018

Danish Medicines Agency aces European benchmark survey

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The Danish Medicines Agency has just scored 4.5 of a possible 5 in the common-European survey known as the Benchmarking of European Medicines Agencies (BEMA). ”It's a really good result that will benefit all of us and may help raise the standard throughout Europe,” said the Danish health minister.

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19-9-2018

Exclusive Brands and iSweet recall Kidsmania Bubble Dozer

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18-9-2018

Lidl Voluntarily Recalls Bellona Brand Hazelnut Wafers Due to Improperly Declared Wheat Allergen

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18-9-2018

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14-9-2018

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13-9-2018

Optipet ad us. vet., Ungezieferhalsband fuer Hunde

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Institut für Veterinärpharmakologie und toxikologie

13-9-2018

Optipet ad us. vet., Ungezieferhalsband fuer Katzen

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Institut für Veterinärpharmakologie und toxikologie

11-9-2018

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PET Ungezieferhalsband fuer Hunde ad us. vet.

PET Ungezieferhalsband fuer Hunde ad us. vet.

● Änderung Text: "Zusammensetzung", "Indikationen" und "Packungen"

Institut für Veterinärpharmakologie und toxikologie

7-9-2018

PET Ungezieferhalsband fuer Katzen ad us. vet.

PET Ungezieferhalsband fuer Katzen ad us. vet.

● Änderung Text "Zusammensetzung", "Indikationen" und "Packungen"

Institut für Veterinärpharmakologie und toxikologie

4-9-2018

Bovilis Blue-8 ad us. vet., Injektionssuspension fuer Rinder und Schafe

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Institut für Veterinärpharmakologie und toxikologie

31-8-2018

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31-8-2018

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22-8-2018

Pexion 100 mg ad us. vet., Tabletten

Pexion 100 mg ad us. vet., Tabletten

● Änderung Text "Unerwünschte Wirkungen" und "Wechselwirkungen"

Institut für Veterinärpharmakologie und toxikologie

22-8-2018

Pexion 400 mg ad us. vet., Tabletten

Pexion 400 mg ad us. vet., Tabletten

● Änderung Text "Unerwünschte Wirkungen" und "Wechselwirkungen"

Institut für Veterinärpharmakologie und toxikologie

17-8-2018

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16-8-2018

Boviseal ad us. vet., Suspension in Injektoren

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● Die Zulassung ist am 16.08.2018 erloschen.

Institut für Veterinärpharmakologie und toxikologie

14-8-2018

Genius Premium Craft Boxes recalls Do-It-Yourself Slime Kits

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9-8-2018

Stronghold Plus ad us. vet. 15 mg / 2,5 mg, Loesung zum Auftropfen fuer Katzen

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● Die Neuzulassung erfolgte am 09.08.2018.

Institut für Veterinärpharmakologie und toxikologie

9-8-2018

Stronghold Plus ad us. vet. 30 mg / 5 mg, Loesung zum Auftropfen fuer Katzen

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● Die Neuzulassung erfolgte am 09.08.2018.

Institut für Veterinärpharmakologie und toxikologie

9-8-2018

Stronghold Plus ad us. vet. 60 mg / 10 mg, Loesung zum Auftropfen fuer Katzen

Stronghold Plus ad us. vet. 60 mg / 10 mg, Loesung zum Auftropfen fuer Katzen

● Die Neuzulassung erfolgte am 09.08.2018.

Institut für Veterinärpharmakologie und toxikologie

7-8-2018

August 6, 2018: Nurse Practitioner Sentenced for Illegally Prescribing Drugs at Substance Abuse Treatment Program

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FDA - U.S. Food and Drug Administration

31-7-2018

Caniquantel plus M ad us. vet., Tabletten

Caniquantel plus M ad us. vet., Tabletten

● Änderung Text "Zusammensetzung", "Eigenschaften / Wirkung", "Indikationen", "Dosierung / Anwendung" und "Sonstige Hinweise"

Institut für Veterinärpharmakologie und toxikologie

31-7-2018

Caniquantel plus S ad us. vet., Tabletten

Caniquantel plus S ad us. vet., Tabletten

● Änderung Text "Zusammensetzung", "Eigenschaften / Wirkung", "Indikationen", "Dosierung / Anwendung" und "Sonstige Hinweise"

Institut für Veterinärpharmakologie und toxikologie

27-7-2018

Scourguard 3 ad us. vet., Injektionssuspension

Scourguard 3 ad us. vet., Injektionssuspension

● Änderung Text alle Rubriken

Institut für Veterinärpharmakologie und toxikologie

26-7-2018

Laxatone ad us. vet., Paste

Laxatone ad us. vet., Paste

● Änderung Text "Zusammensetzung"

Institut für Veterinärpharmakologie und toxikologie

24-7-2018

Final Conference programme JANPA (EN)

Final Conference programme JANPA (EN)

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11-10-2018

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1-10-2018

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26-9-2018

Today, Wednesday, September 26th 2018 at 12 pm EST is the last day that the #FDA will be soliciting site visit proposals for the 2018 Experiential Learning Program. Click the link to find more about the program & submit your application:   http://go.usa.g

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Today, Wednesday, September 26th 2018 at 12 pm EST is the last day that the #FDA will be soliciting site visit proposals for the 2018 Experiential Learning Program. Click the link to find more about the program & submit your application: http://go.usa.gov/xPrum  #MedicalDevice pic.twitter.com/Zsmq00NCdd

FDA - U.S. Food and Drug Administration

24-9-2018

#FDA announces the release of the Collaborative Communities Toolkit for interested stakeholder organizations to work together on healthcare challenges. Learn about the program, download the Toolkit, and submit comments:  https://go.usa.gov/xPjKX pic.twitt

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FDA - U.S. Food and Drug Administration

24-9-2018

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FDA - U.S. Food and Drug Administration

19-9-2018

Reminder: #FDA site visit proposal solicitation period for the 2018  Experiential Learning Program is currently OPEN through Wednesday,  9/26/18 @ 12 pm EST. Click the link to find more about the  program & to submit your application  https://go.usa.gov/x

Reminder: #FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, 9/26/18 @ 12 pm EST. Click the link to find more about the program & to submit your application https://go.usa.gov/x

Reminder: #FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, 9/26/18 @ 12 pm EST. Click the link to find more about the program & to submit your application https://go.usa.gov/xPrum  #MedicalDevice pic.twitter.com/FN1mNN65dD

FDA - U.S. Food and Drug Administration

18-9-2018

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Europe - EMA - European Medicines Agency

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

13-8-2018

Today is Day 1 of the Pediatric Medical Device Development Public Meeting. Today we will discuss the programs, policies, and procedures at the #FDA intended to streamline evidence generation.  https://go.usa.gov/xU6rg 
#devices4kids #Pediatricspic.twitter

Today is Day 1 of the Pediatric Medical Device Development Public Meeting. Today we will discuss the programs, policies, and procedures at the #FDA intended to streamline evidence generation. https://go.usa.gov/xU6rg  #devices4kids #Pediatricspic.twitter

Today is Day 1 of the Pediatric Medical Device Development Public Meeting. Today we will discuss the programs, policies, and procedures at the #FDA intended to streamline evidence generation. https://go.usa.gov/xU6rg  #devices4kids #Pediatrics pic.twitter.com/3tXTgwPJPo

FDA - U.S. Food and Drug Administration

31-7-2018

Join us for the Pediatric Medical Device Development public meeting Aug 13-14 to identify ways to increase the availability of medical devices for children.  https://go.usa.gov/xUvBD  #Pediatrics #medicaldevicepic.twitter.com/ZP3ImzNw2T

Join us for the Pediatric Medical Device Development public meeting Aug 13-14 to identify ways to increase the availability of medical devices for children. https://go.usa.gov/xUvBD  #Pediatrics #medicaldevicepic.twitter.com/ZP3ImzNw2T

Join us for the Pediatric Medical Device Development public meeting Aug 13-14 to identify ways to increase the availability of medical devices for children. https://go.usa.gov/xUvBD  #Pediatrics #medicaldevice pic.twitter.com/ZP3ImzNw2T

FDA - U.S. Food and Drug Administration

31-7-2018

FDA’s Pediatric Device Consortia Grant Program (PDC) facilitates the development, of medical devices for children. 18 pediatric medical devices have been approved/cleared to date.  Learn more about the PDC here:  https://go.usa.gov/xUvBC  #Pediatrics #Med

FDA’s Pediatric Device Consortia Grant Program (PDC) facilitates the development, of medical devices for children. 18 pediatric medical devices have been approved/cleared to date. Learn more about the PDC here: https://go.usa.gov/xUvBC  #Pediatrics #Med

FDA’s Pediatric Device Consortia Grant Program (PDC) facilitates the development, of medical devices for children. 18 pediatric medical devices have been approved/cleared to date. Learn more about the PDC here: https://go.usa.gov/xUvBC  #Pediatrics #MedicalDevice #FDA pic.twitter.com/HgMSCIbmra

FDA - U.S. Food and Drug Administration

31-7-2018

Many medical devices for children may be approved by the Humanitarian Device Exemption pathway. Learn how the Humanitarian Device Exemption pathway program & other pathways can bring more devices intended for children to market.  http://go.usa.gov/xUvZ7 

Many medical devices for children may be approved by the Humanitarian Device Exemption pathway. Learn how the Humanitarian Device Exemption pathway program & other pathways can bring more devices intended for children to market. http://go.usa.gov/xUvZ7 

Many medical devices for children may be approved by the Humanitarian Device Exemption pathway. Learn how the Humanitarian Device Exemption pathway program & other pathways can bring more devices intended for children to market. http://go.usa.gov/xUvZ7  #Pediatrics #medicaldevice pic.twitter.com/LEaSk1efJ5

FDA - U.S. Food and Drug Administration

31-7-2018

On Aug 13-14, the #FDA is hosting the Pediatric Medical Device Development public meeting at the White Oak campus. Join us and participate in discussions around increasing medical device development for children. More info here:  https://go.usa.gov/xUvZm 

On Aug 13-14, the #FDA is hosting the Pediatric Medical Device Development public meeting at the White Oak campus. Join us and participate in discussions around increasing medical device development for children. More info here: https://go.usa.gov/xUvZm 

On Aug 13-14, the #FDA is hosting the Pediatric Medical Device Development public meeting at the White Oak campus. Join us and participate in discussions around increasing medical device development for children. More info here: https://go.usa.gov/xUvZm  #Pediatrics #medicaldevice pic.twitter.com/c0cuVYtTLK

FDA - U.S. Food and Drug Administration

22-7-2018

On Friday, Bayer said the permanent birth control device Essure would no longer be sold or distributed in the US for commercial reasons after 12/31/18. This came after FDA’s patient safety action in April restricting sale and distribution of the device an

On Friday, Bayer said the permanent birth control device Essure would no longer be sold or distributed in the US for commercial reasons after 12/31/18. This came after FDA’s patient safety action in April restricting sale and distribution of the device an

On Friday, Bayer said the permanent birth control device Essure would no longer be sold or distributed in the US for commercial reasons after 12/31/18. This came after FDA’s patient safety action in April restricting sale and distribution of the device and earlier agency actions

FDA - U.S. Food and Drug Administration