Duowin Line On L ad us. vet.

Hauptinformation

  • Handelsname:
  • Duowin® Line On L ad us. vet., Lösung
  • Darreichungsform:
  • Lösung
  • 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:
  • Duowin® Line On L ad us. vet., Lösung
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Ektoparasitenmittel für Hunde

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 54798
  • Letzte Änderung:
  • 02-09-2017

Packungsbeilage

Duowin

Line On L ad us. vet., Lösung

Virbac (Switzerland) AG

Ektoparasitenmittel für Hunde

ATCvet: QP53AX73

Zusammensetzung

100 ml enthalten:

Permethrin

40 g

Pyriproxyfen0,3 g

Antiox: Butylhydroxyanisol E 320, Butylhydroxytoluol E 321

Excip. ad solut.

Fachinformationen Wirkstoffe (CliniPharm)

Permethrin - Pyriproxifen

Eigenschaften / Wirkungen

Permethrin ist ein Molekül der Familie der synthetischen Pyrethroide und zeichnet sich

durch seine schnelle repulsive, insektizide und akarizide Wirkung aus. Das Molekül hemmt

die Übertragung von Nervenimpulsen: Pyrethroide verändern die Durchlässigkeit der

Axonmembran für Na

-Ionen.

Pyriproxyfen ist ein Analogon des Juvenil-Hormons der Insekten. Es verhindert die

Entstehung von adulten Insekten, indem es die biologische Entwicklung der Eier und

Larven blockiert.

Indikationen

Zecken- und Flohbefall bei Hunden.

Wirkung gegen Zecken:

Behandlung und Vorbeugung während 4 Wochen.

Wirkung gegen Flöhe:

Behandlung und Vorbeugung während 4 Wochen.

Vorbeugung einer Vermehrung von Flöhen während 8 Wochen.

Dosierung / Anwendung

Die Dosierung beträgt 0,25 ml Lösung pro kg Körpergewicht. Dies entspricht 100 mg

Permethrin und 0,8 mg Pyriproxyfen pro kg KGW, d.h.:

bei kleinen Hunden ab 2 kg und bis 7,5 kg: 1 Pipette von 2 ml Duowin

Line On S ad us.

vet.

bei mittelgrossen Hunden zwischen 7,5 und 15 kg: 1 Pipette von 4 ml Duowin

Line On M

ad us. vet.

bei grossen Hunden zwischen 15 und 30 kg: 1 Pipette von 8 ml Duowin

Line On L ad

us. vet.

bei sehr grossen Hunden über 30 kg: 2 Pipetten von 8 ml Duowin

Line On L ad us. vet.

Eine Behandlung schützt 4 Wochen vor Befall mit Zecken und Flöhen. Nur zur

äusserlichen Anwendung. Nur Hunde mit trockenem Fell behandeln.

Die Pipette gerade halten. Den Plastikdeckel mit einer Drehbewegung öffnen. Den Inhalt

der Pipette entlang der Rückenlinie des Hundes auftragen.

Dabei regelmässig und sanft auf die Pipette drücken und darauf achten, dass der Ansatz

der Pipette die Haut ständig berührt. Falls etwas Produkt in der Pipette übrig bleibt, dieses

am Schwanzansatz oder zwischen den Schulterblättern auftragen. Den Hund unmittelbar

nach der Behandlung weder waschen noch einshampoonieren.

Anwendungseinschränkungen

Kontraindikationen:

-Nicht bei Katzen anwenden!

-Nicht bei Welpen unter 2 Monaten anwenden.

-Nicht bei kranken oder rekonvaleszenten Tieren anwenden.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

In seltenen Fällen können Juckreiz, Zittern, Erbrechen und Hautrötung beobachtet

werden, die ohne spezielle Behandlung wieder abklingen. Besonders bei Überdosierung

können Hyperästhesie, Ataxie, intensives Erythem oder langanhaltendes Zittern auftreten.

Wechselwirkungen

Nicht gleichzeitig mit anderen Insektiziden anwenden.

Sonstige Hinweise

-Während der Anwendung Haushandschuhe tragen.

Augen- und Hautkontakt vermeiden; sollten Hautpartien mit dem Produkt in Kontakt

geraten sein, diese gründlich mit Wasser abspülen.

-Für Kinder unzugänglich aufbewahren.

-Von Lebensmitteln und Getränken getrennt lagern.

-Das Produkt ist toxisch für Fische und bestimmte in Wasser lebende Organismen.

-Das Arzneimittel nur bis zu dem mit "Exp." bezeichneten Datum verwenden.

Lagerung: Bei Raumtemperatur (15 - 25°C)

Entzündbar.

Packungen

Packungen mit 4 Pipetten zu 8 ml.

Abgabekategorie: B

Hersteller

Virbac S.A. - F 06516 Carros

Swissmedic Nr. 54'798

Informationsstand: 10/2004

Dieser Text ist behördlich genehmigt.

11-10-2018

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10-10-2018

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FDA - U.S. Food and Drug Administration

10-10-2018

Credelio 56 mg ad us. vet., Kautabletten fuer Hunde

Credelio 56 mg ad us. vet., Kautabletten fuer Hunde

● Die Neuzulassung erfolgte am 10.10.2018.

Institut für Veterinärpharmakologie und toxikologie

10-10-2018

Credelio 112 mg ad us. vet., Kautabletten fuer Hunde

Credelio 112 mg ad us. vet., Kautabletten fuer Hunde

● Die Neuzulassung erfolgte am 10.10.2018.

Institut für Veterinärpharmakologie und toxikologie

10-10-2018

Credelio 225 mg ad us. vet., Kautabletten fuer Hunde

Credelio 225 mg ad us. vet., Kautabletten fuer Hunde

● Die Neuzulassung erfolgte am 10.10.2018.

Institut für Veterinärpharmakologie und toxikologie

10-10-2018

Credelio 450 mg ad us. vet., Kautabletten fuer Hunde

Credelio 450 mg ad us. vet., Kautabletten fuer Hunde

● Die Neuzulassung erfolgte am 10.10.2018.

Institut für Veterinärpharmakologie und toxikologie

10-10-2018

Credelio 900 mg ad us. vet., Kautabletten fuer Hunde

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● Die Neuzulassung erfolgte am 10.10.2018.

Institut für Veterinärpharmakologie und toxikologie

9-10-2018

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

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● Verzicht Packungsgrösse 10 ml

Institut für Veterinärpharmakologie und toxikologie

3-10-2018

Metacam 2 mg/ml Katzen ad us. vet., Injektionsloesung

Metacam 2 mg/ml Katzen ad us. vet., Injektionsloesung

● Verzicht Packungsgrösse 20 ml

Institut für Veterinärpharmakologie und toxikologie

2-10-2018

Forthyron 200 ad us. vet., Tabletten

Forthyron 200 ad us. vet., Tabletten

● Die Zulassung ist am 02.10.2018 erloschen.

Institut für Veterinärpharmakologie und toxikologie

2-10-2018

Forthyron 400 ad us. vet., Tabletten

Forthyron 400 ad us. vet., Tabletten

● Die Zulassung ist am 02.10.2018 erloschen.

Institut für Veterinärpharmakologie und toxikologie

26-9-2018

Technical Report on the notification of syrup from Sorghum bicolor (L.) Moench as a traditional food from a third country pursuant to Article 14 of Regulation (EU) 2015/2283

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Published on: Tue, 25 Sep 2018 00:00:00 +0200 Abstract Following a notification from Sorghum Zrt., submitted to the European Commission under Article 14 of Regulation (EU) 2015/2283 to place on the market syrup from Sorghum bicolor (L.) Moench as a traditional food from a third country (TF), and in line with Article 15(2) of that Regulation, EFSA was asked by the European Commission whether there are duly reasoned safety objections to the placing on the market of the TF within the European Union. The ap...

Europe - EFSA - European Food Safety Authority Publications

26-9-2018

Gleptosil ad us. vet., Injektionsloesung

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● Änderung Text "Zusammensetzung", "Unerwünschte Wirkungen" und zusätzliche Packungsgrösse: 250 ml

Institut für Veterinärpharmakologie und toxikologie

21-9-2018

Scientific guideline:  Guideline on determination of withdrawal periods for edible tissues - Revision 1, adopted

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Europe - EFSA - European Food Safety Authority EFSA Journal

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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FDA - U.S. Food and Drug Administration

20-9-2018

Health Canada warns consumers to not use health products containing the potentially dangerous chemical DNP

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Health Canada

20-9-2018

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

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● Die Neuzulassung erfolgte am 20.09.2018.

Institut für Veterinärpharmakologie und toxikologie

20-9-2018

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

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● Die Neuzulassung erfolgte am 20.09.2018.

Institut für Veterinärpharmakologie und toxikologie

19-9-2018

Danish Medicines Agency aces European benchmark survey

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Danish Medicines Agency

18-9-2018

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

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FDA - U.S. Food and Drug Administration

14-9-2018

Development of an automated multienzymatic biosensor for risk assessment of pesticide contamination in water and food

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13-9-2018

Optipet ad us. vet., Ungezieferhalsband fuer Hunde

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● Die Neuzulassung erfolgte am 13.09.2018.

Institut für Veterinärpharmakologie und toxikologie

13-9-2018

Optipet ad us. vet., Ungezieferhalsband fuer Katzen

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● Die Neuzulassung erfolgte am 13.09.2018.

Institut für Veterinärpharmakologie und toxikologie

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September 6, 2018: Cattle Company and Veterinarian Indicted for False Health Certificates on Livestock

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10-9-2018

Jay Trends Inc. recalls Tempered Glass of the Sunbeam Linear Fire Table

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PET Ungezieferhalsband fuer Hunde ad us. vet.

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

Institut für Veterinärpharmakologie und toxikologie

7-9-2018

PET Ungezieferhalsband fuer Katzen ad us. vet.

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

Institut für Veterinärpharmakologie und toxikologie

6-9-2018

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FDA - U.S. Food and Drug Administration

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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30-8-2018

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FDA - U.S. Food and Drug Administration

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

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● Änderung Text "Unerwünschte Wirkungen" und "Wechselwirkungen"

Institut für Veterinärpharmakologie und toxikologie

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

9-8-2018

Dringende Sicherheitsinformation zu Sterile Kundensets inkl. ophthalmische Marker von Medline International France SAS

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Weitere Informationen sowie Details zum Produkt entnehmen Sie bitte der anliegenden Kundeninformation des Herstellers.

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

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

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● Die Neuzulassung erfolgte am 09.08.2018.

Institut für Veterinärpharmakologie und toxikologie

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

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● Änderung Text alle Rubriken

Institut für Veterinärpharmakologie und toxikologie

26-7-2018

Trek Bicycle Corporation recalls Bontrager Line Pro Flat Bicycle Pedals

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The pedals may have been manufactured with hydrogen embrittlement in the spindle of the pedals, causing one or both of the pedals to fail. When it fails, the pedal body separates from the spindle. If this happens while the bicycle is being operated, the rider could potentially lose control of the bicycle and fall.

Health Canada

26-7-2018

Laxatone ad us. vet., Paste

Laxatone ad us. vet., Paste

● Änderung Text "Zusammensetzung"

Institut für Veterinärpharmakologie und toxikologie

24-7-2018

Dringende Sicherheitsinformation zu Applimed cannula needle straight with olive, 100mm, stainless steel, G18,diameter 1.19mm, included in Medline Sterile Procedure Trays von Medline International France SAS

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Weitere Informationen sowie Details zum Produkt entnehmen Sie bitte der anliegenden Kundeninformation des Herstellers.

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

21-7-2018

GiftTree Issues Allergy Alert on Undeclared Pecans, Walnuts, Almonds, Peanuts in " Sherman Candy Caramels "

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FDA - U.S. Food and Drug Administration

18-7-2018

sera med Professional Ophionol ad us. vet. , Loesung

sera med Professional Ophionol ad us. vet. , Loesung

● Erneute Zulassung

Institut für Veterinärpharmakologie und toxikologie

18-7-2018

sera med Professional Oxyspirol ad us. vet., Loesung

sera med Professional Oxyspirol ad us. vet., Loesung

● Erneute Zulassung

Institut für Veterinärpharmakologie und toxikologie

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

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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

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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

1-10-2018

IONSYS (Incline Therapeutics Europe Ltd)

IONSYS (Incline Therapeutics Europe Ltd)

IONSYS (Active substance: fentanyl) - Centralised - Withdrawal - Commission Decision (2018)6412 of Mon, 01 Oct 2018

Europe -DG Health and Food Safety

28-8-2018

EU/3/18/2057 (Pharm Research Associates (UK) Limited)

EU/3/18/2057 (Pharm Research Associates (UK) Limited)

EU/3/18/2057 (Active substance: 1-(2-hydroxyethyl)-8-{[5-(4-methylpiperazin-1-yl)-2-(trifluoromethoxy) phenyl]amino}-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide fumarate salt) - Orphan designation - Commission Decision (2018)5729 of Tue, 28 Aug 2018 European Medicines Agency (EMA) procedure number: EMA/OD/051/18

Europe -DG Health and Food Safety

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

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

31-7-2018

Consumers face health risks buying erectile dysfunction medicines online

Consumers face health risks buying erectile dysfunction medicines online

The TGA is warning consumers to consult with their doctor prior to purchasing medicines for erectile dysfunction from overseas websites

Therapeutic Goods Administration - Australia

30-7-2018

Special Access Scheme online system

Special Access Scheme online system

Introduction of the Special Access Scheme online system

Therapeutic Goods Administration - Australia

27-7-2018

Australian regulatory guidelines for biologicals (ARGB)

Australian regulatory guidelines for biologicals (ARGB)

The ARGB has been restructured and updated in line with new legislative changes

Therapeutic Goods Administration - Australia

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