API-Bioxal ad us. vet.[B]

Hauptinformation

  • Handelsname:
  • API-Bioxal® ad us. vet.[B], Pulver
  • Darreichungsform:
  • Pulver
  • 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-Bioxal® ad us. vet.[B], Pulver
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Zur Behandlung der Varroose bei Honigbienen (Apis mellifera)

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 65974
  • Letzte Änderung:
  • 02-09-2017

Packungsbeilage

API-Bioxal

ad us. vet.

, Pulver

Befristete

Zulassungen

Swissmedic

Bienen Meier AG

Zur Behandlung der Varroose bei Honigbienen (Apis mellifera)

ATCvet: QP53AG03

Zusammensetzung

100 g des Produktes enthalten

88.6 g Oxalsäuredihydrat (acidum oxalicum dihydricum)

Pharmazeutische Hilfsstoffe ad 100 g

Lösliches Pulver

Fachinformationen Wirkstoffe (CliniPharm)

Oxalsäure

Eigenschaften / Wirkungen

API-Bioxal ist ein Oxalsäurepräparat, das als Träufellösung oder als Sublimat (mittels

Verdampfer) zur Behandlung der Varroose eingesetzt wird. Die abtötende Wirkung von

Oxalsäure bei der Varroamilbe basiert hauptsächlich auf deren Säure-Eigenschaft.

Oxalsäure wirkt nur auf Varroamilben, die sich auf den Bienen befinden. Sie zeigt keine

Wirkung auf Milben in verdeckelter Brut.

Indikationen

Behandlung der Varroose (Befall mit Varroa destructor) bei der Honigbiene (Apis mellifera)

in brutfreien Bienenvölkern.

Dosierung / Anwendung

Für die grösstmögliche Wirkung darf keine Brut vorhanden sein. Die Behandlung

vornehmen, wenn sich keine Honigwaben in den Beuten befinden. Alle Völker gleichzeitig

behandeln, um einen Neubefall zu vermeiden. Manipulationen an den Völkern in den

Tagen nach der Behandlung vermeiden.

Das Präparat wird in folgenden Arten und Dosierungen angewendet:

a) Träufellösung

Beutelinhalt lösen in der angegebenen Menge Sirup (Wasser und Saccharose im

Verhältnis 1:1)

Beutel à 35 g API-Bioxal: Lösen in 890 ml Sirup

Beutel à 175 g API-Bioxal: Lösen in 4.4 l Sirup

Beutel à 350 g API-Bioxal: Lösen in 8.8 l Sirup

Die Behandlung muss durch eine einmalige Anwendung erfolgen, indem mit einer

geeigneten Plastikspritze je bienenbesetzte Wabengasse 5 ml gebrauchsfertige Lösung

geträufelt wird.

b) Sublimation

-Dosierung Schweizerkasten und Beuten mit einer Zarge 1.15 g API-Bioxal

-Dosierung Dadant-Beuten und Beuten mit 2 Zargen 2.3 g API-Bioxal

-Die erforderliche Menge Pulver auf das/in das ausgeschaltete Gerät geben.

Gerät durch ein Loch (z.B. Flugloch) in die Beute einführen und dabei Kontakt mit Waben

vermeiden.

Beute abdichten, um den Ausflug der Bienen und das Austreten der Dämpfe zu

verhindern.

Gerät gemäss Anleitung ein- und ausschalten und Abdichtung einige Minuten nach dem

Abschalten wieder entfernen.

Betriebsanleitung des Geräteherstellers beachten.

Anwendungseinschränkungen

API-Bioxal nur in brutfreien Phasen (Winterbehandlung) oder bei künstlich herbeigeführter

Brutfreiheit (z.B. Natur- oder Kunstschwarm) anwenden. Das Vorhandensein von Brut

kann die Wirksamkeit spürbar reduzieren.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Das Volk kann während der Behandlung ein leicht aufgeregtes Verhalten zeigen.

Absetzfristen

Honig: Keine.

Wechselwirkungen

Nicht gleichzeitig mit anderen milbenabtötenden Mitteln verwenden.

Sonstige Hinweise

Das Produkt nicht kühlen oder einfrieren und vor direktem Sonnenlicht geschützt in der

Originalpackung aufbewahren. Den Beutel nach dem Öffnen sorgfältig wieder

verschliessen, um das Arzneimittel gegen Feuchtigkeit zu schützen.

Haut- und Augenkontakt vermeiden, stets undurchlässige Handschuhe und Schutzbrille

tragen. Beim Umgang mit dem pulverförmigen Produkt (auch bei der Behandlung)

zusätzlich Schutzmaske Typ FFP2 tragen. Nach der Anwendung des Produktes Hände

und andere mit diesem in Kontakt gekommene Gegenstände mit Wasser und Seife

waschen. Bei Kontakt des Produktes mit den Augen, diese sorgfältig unter fliessendem

Wasser spülen und einen Arzt konsultieren. Das Produkt darf nicht in Wasserläufe

gelangen, da es für Wasserlebewesen gefährlich sein könnte.

Für Kinder unzugänglich aufbewahren.

Nach dem Öffnen des Beutels diesen wieder gut verschliessen und das Pulver innerhalb

der nachfolgenden 3 Monate aufbrauchen.

Packungen

Beutel à 35 g API-Bioxal

Beutel à 175 g API-Bioxal

Beutel à 350 g API-Bioxal

Abgabekategorie: D

Swissmedic Nr. 65'974

Informationsstand: 08/2015

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November is #DiabetesAwarenessMonth  #DYK using a glucose meter to check and monitor blood sugar is a daily part of life for millions of Americans with diabetes? Check out the @US_FDA's tips on how to safely use glucose meters and test strips for diabetes

November is #DiabetesAwarenessMonth #DYK using a glucose meter to check and monitor blood sugar is a daily part of life for millions of Americans with diabetes? Check out the @US_FDA's tips on how to safely use glucose meters and test strips for diabetes

November is #DiabetesAwarenessMonth #DYK using a glucose meter to check and monitor blood sugar is a daily part of life for millions of Americans with diabetes? Check out the @US_FDA's tips on how to safely use glucose meters and test strips for diabetes: https://go.usa.gov/xPdK4 

FDA - U.S. Food and Drug Administration

6-11-2018

Arilin® Rapid Vaginalzäpfchen

Rote - Liste

2-11-2018

.@US_FDA  issues a class I recall: Roche Diagnostics recalls CoaguChek  XS PT Test  Strips due to inaccurate INR test results. Find out more:  https://go.usa.gov/xPVER  #FDA #MedicalDevicepic.twitter.com/EYmVZHrUZc

.@US_FDA issues a class I recall: Roche Diagnostics recalls CoaguChek XS PT Test Strips due to inaccurate INR test results. Find out more: https://go.usa.gov/xPVER  #FDA #MedicalDevicepic.twitter.com/EYmVZHrUZc

. @US_FDA issues a class I recall: Roche Diagnostics recalls CoaguChek XS PT Test Strips due to inaccurate INR test results. Find out more: https://go.usa.gov/xPVER  #FDA #MedicalDevice pic.twitter.com/EYmVZHrUZc

FDA - U.S. Food and Drug Administration

2-11-2018

Check out @US_FDA's information on Direct-to-Consumer Tests:  https://go.usa.gov/xPVPu  #MedicalDevice #FDA

Check out @US_FDA's information on Direct-to-Consumer Tests: https://go.usa.gov/xPVPu  #MedicalDevice #FDA

Check out @US_FDA's information on Direct-to-Consumer Tests: https://go.usa.gov/xPVPu  #MedicalDevice #FDA

FDA - U.S. Food and Drug Administration

2-11-2018

#DYK the @US_FDA recently authorized the first direct-to-consumer test   for detecting genetic variants that may be associated with medication   metabolism? Learn more about the authorization:  https://go.usa.gov/xPVUt  #MedicalDevice #FDA

#DYK the @US_FDA recently authorized the first direct-to-consumer test for detecting genetic variants that may be associated with medication metabolism? Learn more about the authorization: https://go.usa.gov/xPVUt  #MedicalDevice #FDA

#DYK the @US_FDA recently authorized the first direct-to-consumer test for detecting genetic variants that may be associated with medication metabolism? Learn more about the authorization: https://go.usa.gov/xPVUt  #MedicalDevice #FDA

FDA - U.S. Food and Drug Administration

1-11-2018

The @US_FDA issues a letter to health care providers regarding possible battery failure in Getinge's Maquet/Datascope intra-aortic balloon pumps. Read the letter here:  https://go.usa.gov/xPyHT  #MedicalDevice

The @US_FDA issues a letter to health care providers regarding possible battery failure in Getinge's Maquet/Datascope intra-aortic balloon pumps. Read the letter here: https://go.usa.gov/xPyHT  #MedicalDevice

The @US_FDA issues a letter to health care providers regarding possible battery failure in Getinge's Maquet/Datascope intra-aortic balloon pumps. Read the letter here: https://go.usa.gov/xPyHT  #MedicalDevice

FDA - U.S. Food and Drug Administration

1-11-2018

The @US_FDA warns patients & health care providers should not change drug treatment based on results from certain genetic tests w/ unapproved claims to predict a patient’s response to specific medications. Read the Safety Communication here:  https://go.u

The @US_FDA warns patients & health care providers should not change drug treatment based on results from certain genetic tests w/ unapproved claims to predict a patient’s response to specific medications. Read the Safety Communication here: https://go.u

The @US_FDA warns patients & health care providers should not change drug treatment based on results from certain genetic tests w/ unapproved claims to predict a patient’s response to specific medications. Read the Safety Communication here: https://go.usa.gov/xPysF  #MedicalDevice

FDA - U.S. Food and Drug Administration

31-10-2018

Quetiapin-Hormosan Filmtabletten

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

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

19-10-2018

New Safety Communication. @US_FDA   is sharing Updated Information To Reduce Potential Cardiac Surgery   Infection Risks Associated With the LivaNova 3T Heater-Cooler Systems. Read More:  https://go.usa.gov/xPnNW  #FDA #MedicalDevice

New Safety Communication. @US_FDA is sharing Updated Information To Reduce Potential Cardiac Surgery Infection Risks Associated With the LivaNova 3T Heater-Cooler Systems. Read More: https://go.usa.gov/xPnNW  #FDA #MedicalDevice

New Safety Communication. @US_FDA is sharing Updated Information To Reduce Potential Cardiac Surgery Infection Risks Associated With the LivaNova 3T Heater-Cooler Systems. Read More: https://go.usa.gov/xPnNW  #FDA #MedicalDevice

FDA - U.S. Food and Drug Administration

17-10-2018

Save the date & Join the @US_FDA’s  Patient Engagement Advisory Committee on Nov 15th to discuss  patient-generated health data from sources like social media, activity  trackers, and patient-driven registries. Learn more:  https://go.usa.gov/xPRau  #Digi

Save the date & Join the @US_FDA’s Patient Engagement Advisory Committee on Nov 15th to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries. Learn more: https://go.usa.gov/xPRau  #Digi

Save the date & Join the @US_FDA’s Patient Engagement Advisory Committee on Nov 15th to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries. Learn more: https://go.usa.gov/xPRau  #DigitalHealth #PEAC2018 pic.twitter.com/NU61Snpxxw

FDA - U.S. Food and Drug Administration

15-10-2018

We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4.

 http://fema.gov/hurricane-michael-rumor-co

We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4. http://fema.gov/hurricane-michael-rumor-co

We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4. http://fema.gov/hurricane-michael-rumor-control … pic.twitter.com/T3h7ZiFUrZ

FDA - U.S. Food and Drug Administration

10-10-2018

Diversity in research means more treatments work for more people. Join #ResearchDiversity Day on October 23rd for a day-long discussion of diversity in study recruitment and research. Join us! @Alzheimers_NIHpic.twitter.com/AwYhetCBiw

Diversity in research means more treatments work for more people. Join #ResearchDiversity Day on October 23rd for a day-long discussion of diversity in study recruitment and research. Join us! @Alzheimers_NIHpic.twitter.com/AwYhetCBiw

Diversity in research means more treatments work for more people. Join #ResearchDiversity Day on October 23rd for a day-long discussion of diversity in study recruitment and research. Join us! @Alzheimers_NIH pic.twitter.com/AwYhetCBiw

FDA - U.S. Food and Drug Administration