Api Life Var ad us. vet.

Hauptinformation

  • Handelsname:
  • Api Life Var® ad us. vet., Evaporationsplättchen
  • Darreichungsform:
  • Evaporationsplättchen
  • 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:
  • Api Life Var® ad us. vet., Evaporationsplättchen
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Zur Bekämpfung der Varroamilben in Bienenvölkern

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 60557
  • Letzte Änderung:
  • 02-09-2017

Packungsbeilage

Api Life Var

ad us. vet., Evaporationsplättchen

Bienen Meier AG

Zur Bekämpfung der Varroamilben in Bienenvölkern

ATCvet: QP53AX22

Zusammensetzung

100 g des Produktes enthalten

Thymol 76.0 g/ Eucalyptusoel 16.4 g/ Kampfer 3.8 g/ Levomenthol - Trägermaterial

Fachinformationen Wirkstoffe (CliniPharm)

Campher - Eukalyptusöl - Menthol - Thymol

Eigenschaften / Wirkungen

Api Life Var ist eine Mischung aus ätherischen Komponenten. Die synergistischen Effekte

von Thymol, Eucalyptusoel, Menthol und Kampfer sollen einen Milbenbefall, im

Besonderen mit Varroamilben (Varroa destructor), wirkungsvoll bekämpfen. Durch

Verdunsten werden die Wirkstoffe freigesetzt und in der Stockluft angereichert. Durch

direkten Kontakt fallen die Milben von den infizierten Bienen ab.

Indikationen

Api Life Var - Verdunstungsplättchen wird verwendet zur Vorbeugung und Bekämpfung

der Varroose der Bienen (Varroa destructor).

Dosierung / Anwendung

Der optimale Behandlungsbeginn dürfte unter schweizerischen Bedingungen direkt nach

der Sommer-Honigernte ab 1. - 15. August liegen. Ein Teil der Auffütterung ist vor

Behandlungsbeginn durchzuführen. Die restliche Winterauffütterung erfolgt zwischen der

ersten und der zweiten Behandlung. Dauer der Behandlung beträgt insgesamt 6 bis

8 Wochen (zweimal drei bzw. vier Wochen). Falls wegen Spättracht der

Behandlungsbeginn erst im September möglich ist, kann die Wirksamkeit reduziert sein.

Für jedes Bienenvolk sind 2 Plastikbeutel mit total 4 Api Life Var Plättchen zu verwenden.

CH-Kasten

Erste Behandlung von 3 bis 4 Wochen: je ein Plättchen vor und hinter das Brutnest legen.

Zweite Behandlung von 3 bis 4 Wochen: je ein Plättchen vor und hinter das Brutnest

legen.

Magazinbeuten Typ Dadant

Erste Behandlung von 3 bis 4 Wochen ein Plättchen vor und je ½ Plättchen links und

rechts des Brutnestes legen. Zweite Behandlung von 3 bis 4 Wochen ein Plättchen vor

und je ½ Plättchen links und rechts des Brutnestes legen.

Bei einer Behandlung von unten ist der Erfolg bedeutend geringer. Damit die Bienen die

Tafeln nicht abtragen, kann ein bienendichtes Gitter zwischen Brutwaben und Tafel gelegt

werden. Nach der Behandlung sollen die Restplättchen entfernt werden. Im Rahmen eines

integrierten Behandlungskonzeptes wird eine Kombination mit einer späteren

Oxalsäurebehandlung empfohlen, wenn die Völker bruffrei sind.

Anwendungseinschränkungen

Kontraindikationen

Keine bekannt

Vorsichtsmassnahmen

Die Dosierung darf nicht überschritten werden. Sicherstellen, dass keine Räuberei unter

den Bienenvölkern stattfindet. Die Winterauffütterung sollte wenn möglich vor und

zwischen den beiden Behandlungen erfolgen. Es wird empfohlen, die Völker nur bei

Temperaturen unter 27 - 30 °C zu behandeln. Höhere Temperaturen steigern die

Wirksamkeit nicht. Hingegen könnten die Bienen Schaden nehmen. Minimale Temperatur

18 °C.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Es kommt vor, dass die Bienen das Winterfutter und die Brut aus dem Bereich der

Plättchen wegtragen. Die restlichen Gaben des Winterfutters werden manchmal von den

Bienen schlecht abgenommen.

Während der Behandlung dürfen keine Honigwaben in der Beute sein. Bei der

Frühjahrshonigernte dürfen keine Waben aus dem Brutraum mitgeschleudert werden.

Wechselwirkungen

Nicht gleichzeitig mit anderen Milbenmitteln verwenden.

Sonstige Hinweise

Nicht inhalieren, nicht einnehmen. Augen- und Hautkontakt vermeiden. Handschuhe

verwenden. Keine offenen Packungen verwenden. Verfallene und verbrauchte Plättchen

mit dem Hauskehricht entsorgen. Bei Raumtemperatur (15 - 25 °C) lagern. Vor direkter

Sonneneinstrahlung schützen. Für Kinder unzugänglich aufbewahren.

Haltbarkeit: 2 Jahre.

Packungen

Plastikbeutel mit 2 Plättchen

Abgabekategorie: D

Hersteller

CHEMICALS LAIF SRL 35010 Vigonza (PD) I

Swissmedic Nr. 60'557

Informationsstand: 11/2010

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FDA - U.S. Food and Drug Administration

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18-5-2018

7K and Poseidon 4500 by Shoreside Enterprises: Voluntary Recall - Due to Presence of Undeclared Sildenafil and/or Tadalafil

7K and Poseidon 4500 by Shoreside Enterprises: Voluntary Recall - Due to Presence of Undeclared Sildenafil and/or Tadalafil

Use of products with the undeclared active ingredients, sildenafil and tadalafil, may pose a threat to consumers because the active ingredient may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening. Among the adult male population who are most likely to use these products, adult males who use nitrates for cardiac conditions are the most at risk from these products. These products are considered ta...

FDA - U.S. Food and Drug Administration

17-5-2018

BLM Issues Allergy Alert On Undeclared Egg and Milk

BLM Issues Allergy Alert On Undeclared Egg and Milk

BLM Prod.-u. Vertriebsges. mbH & Co. KG, is voluntarily recalling Priano Rosso Pesto Sauce as it may contain undeclared milk and egg. People who have an allergy or severe sensitivity to milk and egg run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

17-5-2018

ufamed Colistin 500 ad us. vet., Arzneimittelvormischung

ufamed Colistin 500 ad us. vet., Arzneimittelvormischung

● Verzicht Packungsgrösse 25 kg

Institut für Veterinärpharmakologie und toxikologie

16-5-2018

Mas Food Services Co. Issues Allergy Alert on Undeclared Sulfites in The Peruchef Dry Potato

Mas Food Services Co. Issues Allergy Alert on Undeclared Sulfites in The Peruchef Dry Potato

Mas Food Services Co. of Oakland Park, FL is recalling its 15 ounce packages of The Peruchef brand dry potato because it may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

15-5-2018

Bovilis Bovigrip ad us. vet., Injektionssuspension

Bovilis Bovigrip ad us. vet., Injektionssuspension

● Änderung Text alle Rubriken

Institut für Veterinärpharmakologie und toxikologie

12-5-2018

Sugarfina, Inc.  Issues Allergen Labeling Alert for Undeclared Eggs in Sugar Cookies Product

Sugarfina, Inc. Issues Allergen Labeling Alert for Undeclared Eggs in Sugar Cookies Product

Sugarfina, Inc. is recalling its Sugar Cookies product because the label does not declare that this product contains egg. People who have allergies or severe sensitivities to eggs run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

11-5-2018

Cevazuril 50 mg/ml ad us. vet., orale Suspension

Cevazuril 50 mg/ml ad us. vet., orale Suspension

● Verfügbarkeit: nicht erhältlich (Ausverkauft / Nicht lieferbar)

Institut für Veterinärpharmakologie und toxikologie

11-5-2018

Tetrawest N ad us. vet., Pulver

Tetrawest N ad us. vet., Pulver

● Verfügbarkeit: nicht erhältlich (Ausverkauft / Nicht lieferbar)

Institut für Veterinärpharmakologie und toxikologie

17-7-2018

The #FDA invites you to join us and discuss how we can increase medical device options for children at the Pediatric Medical Device Development public meeting. Click the link to register.  #Pediatrics  https://go.usa.gov/xUXHq  #MedicalDevicepic.twitter.c

The #FDA invites you to join us and discuss how we can increase medical device options for children at the Pediatric Medical Device Development public meeting. Click the link to register. #Pediatrics https://go.usa.gov/xUXHq  #MedicalDevicepic.twitter.c

The #FDA invites you to join us and discuss how we can increase medical device options for children at the Pediatric Medical Device Development public meeting. Click the link to register. #Pediatrics https://go.usa.gov/xUXHq  #MedicalDevice pic.twitter.com/hL7vawmOgR

FDA - U.S. Food and Drug Administration

22-6-2018

News and press releases:  Reinforced EU/US collaboration on medicines

News and press releases: Reinforced EU/US collaboration on medicines

Update on the European Commission/EMA–FDA bilateral of 18-19 June 2018

Europe - EMA - European Medicines Agency

20-6-2018

Share your thoughts with us in the 2018 TGA surveys

Share your thoughts with us in the 2018 TGA surveys

Our annual survey measures satisfaction with a range of services and activities including our role and performance

Therapeutic Goods Administration - Australia

1-6-2018

News and press releases:  Two more EU Member States benefit from EU-US mutual recognition agreement for inspections

News and press releases: Two more EU Member States benefit from EU-US mutual recognition agreement for inspections

Agreement now operational between 14 EU Member States and FDA

Europe - EMA - European Medicines Agency

24-5-2018

News and press releases:  Development of antibiotics for children - towards a global approach

News and press releases: Development of antibiotics for children - towards a global approach

Workshop with regulators from EU, Japan and US open for registration

Europe - EMA - European Medicines Agency

14-5-2018

Celebrate National Women’s Health Week by joining us this Wednesday at 1 p.m. ET for “The Great Debate: What is Enough… Women in Clinical Trials”.  http://ow.ly/GF8m30jTpFn  #NWHW #clinicaltrialspic.twitter.com/mvltDqmK8v

Celebrate National Women’s Health Week by joining us this Wednesday at 1 p.m. ET for “The Great Debate: What is Enough… Women in Clinical Trials”. http://ow.ly/GF8m30jTpFn  #NWHW #clinicaltrialspic.twitter.com/mvltDqmK8v

Celebrate National Women’s Health Week by joining us this Wednesday at 1 p.m. ET for “The Great Debate: What is Enough… Women in Clinical Trials”. http://ow.ly/GF8m30jTpFn  #NWHW #clinicaltrials pic.twitter.com/mvltDqmK8v

FDA - U.S. Food and Drug Administration