LincoNeo Mast ad us. vet.

Hauptinformation

  • Handelsname:
  • LincoNeo Mast 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.


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Lokalisierung

  • Erhältlich in:
  • LincoNeo Mast ad us. vet., Lösung
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Euterinjektoren für Milchkühe

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 54334
  • Letzte Änderung:
  • 22-01-2018

Packungsbeilage: zusammensetzung, kinische angaben, nebenwirkungen, wechselwirkungen, dosierung, schwangerschaft, stillzeit

LincoNeo Mast ad us. vet., Lösung

PDF-Version:

Français

Virbac (Switzerland) AG

Euterinjektoren für Milchkühe

ATCvet: QJ51RF03

Zusammensetzung

Lincomycinum 330 mg ut Lincomycini hydrochloridum, Neomycinum 100 mg ut Neomycini

sulfas, Dinatrii edetas, Aqua ad iniectabilia q.s. ad solutionem pro 10 ml.

Fachinformationen Wirkstoffe (CliniPharm)

Lincomycin - Neomycin

Eigenschaften / Wirkungen

Lincomycin:

Die antibakterielle Aktivität von Lincomycin, das zur Gruppe der Lincosamide gehört,

richtet sich vor allem gegen grampositive Aerobier, Anaerobier und Mycoplasmen.

Lincomycin ist gegen folgende Erreger wirksam:

Aerobier: Staphylokokken, einschliesslich laktamaseproduzierender Stämme,

Streptokokken, einschliesslich β-haemolysierender Streptokokken, Erysipelotrix,

Leptospiren, Mycoplasmen.

Anaerobier: Clostridien, Actinomyces, Bacteroides, Serpulina hyodysenteriae.

Lincomycin hemmt durch eine reversible Bindung an die 50-S-Untereinheit der

Bakterienribosomen die bakterielle Proteinsynthese. Je nach Empfindlichkeit und

Konzentration ist die antibakterielle Wirkung somit bakteriostatisch oder bakterizid. Die

Resistenzentwicklung erfolgt langsam nach dem "slow-multistage"-Typ.

Neomycin:

Das Wirkungsspektrum von Neomycin umfasst zahlreiche grampositive und gramnegative

Bakterien (Staphylokokkus aureus, Streptokokkus spp., E. coli, Pseudomonas aeruginosa,

Enterobacter aerogenes, Proteus vulgaris, Arten von Brucella, Pasteurella, Campylobacter

und Salmonella sowie Mykobakterium). Neomycin wirkt bakterizid durch Hemmung der

bakteriellen Proteinsynthese. Der Angriffspunkt ist die 30-S-Untereinheit der Bakterien-

ribosomen, wobei es zu einer Hemmung der Proteinsynthese und zu Fehlern in der

Translation des genetischen Codes an der m-RNS kommt. Eine vorliegende Resistenz

gegen Neomycin erstreckt sich meist auch auf Kanamycin, z. T. auch auf Gentamicin und

Dihydrostreptomycin.

Lincomycin und Neomycin in Kombination:

In-vitro-Studien haben gezeigt, dass diese Kombination bakterizid wirksam ist gegen S.

aureus und E. coli und bakteriostatisch wirksam gegen Streptokokkus spp. Ein

Synergismus wurde gegen Staphylokokkus aureus nachgewiesen.

Pharmakokinetik

Bei vorschriftsmässiger Anwendung können folgende mittlere Konzentrationen von

Lincomycin und Neomycin in jedem behandelten Viertel gemessen werden:

Antibiotikum

Lincomycin Neomycin

Konzentration (µg/ml) vor der Instillation des 2. Injektors

52,7

27,2

Konzentration (µg/ml) vor der Instillation des 3. Injektors

53,5

29,9

Konzentration (µg/ml) 12 Stunden nach der Instillation des

3. Injektors

56,9

28,0

Konzentration (µg/ml) 24 Stunden nach der Instillation des

3. Injektors

Therapeutisch wirksame Spiegel oberhalb der MHK werden über die gesamte

Behandlungsdauer und mindestens 12 Stunden danach aufrechterhalten.

Indikationen

Zur Behandlung der durch lincomycin- und neomycinempfindliche Erreger

hervorgerufenen Euterentzündungen bei laktierenden Kühen, verursacht durch:

Staphylokokkus aureus, Streptokokkus agalactiae, Streptokokkus dysgalactiae,

Streptokokkus uberis und Escherichia coli.

Dosierung / Anwendung

1 Injektor (10 ml LincoNeo Mast) pro erkranktes Viertel 3-mal in 12-stündigem Abstand.

Insgesamt sind 3 Behandlungen pro erkranktes Viertel durchzuführen.

Vor der Behandlung die Zitzen gründlich reinigen, das Euter vollständig ausmelken und

den Strichkanal desinfizieren. Inhalt des Injektors nach Einführen der passenden

Injektorspritze in den Zitzenkanal instillieren. Danach das Viertel massieren, um das

Produkt in der Milchzisterne zu verteilen. Nach der Instillation die Zitzen mit einem

Zitzentauchmittel behandeln.

Anwendungseinschränkungen

Kontraindikationen

Resistenzen und Überempfindlichkeit gegen Aminoglykoside und Lincosamide. Bei

vorliegender Leberfunktionsstörung sollte LincoNeo Mast nicht angewendet werden. Nicht

kombinieren mit anderen Aminoglykosiden oder bakteriostatisch wirkenden Antibiotika.

Vorsichtsmassnahmen

Keine notwendig.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Bisher keine bekannt.

Essbare Gewebe:3 Tage

Milch:

6 Tage

Wechselwirkungen

Zwischen Lincomycin und Clindamycin besteht komplette Kreuzresistenz; gegenüber

Makrolid-Antibiotika wie Erythromycin, Kitasamycin, Spiramycin und Oleandomycin

partielle Kreuzresistenz.

Bei gleichzeitiger Anwendung von Anästhetika bzw. Wirkstoffen mit neuromuskulärer

Blockadewirkung (z.B. Tubocurarin, Gallamin, Pancuronium) verstärkt Lincomycin die

Curare-ähnlichen Effekte dieser Muskelrelaxantien.

Sonstige Hinweise

Lagerung bei Raumtemperatur (15 - 25°C).

Ausserhalb der Reichweite von Kindern aufbewahren.

Das Arzneimittel darf nur bis zu dem auf dem Behälter mit "EXP" angegebenen Datum

verwendet werden.

Packungen

Packung mit 24 × 10 ml

Abgabekategorie: A

Swissmedic Nr. 54'334

Informationsstand: 10/2007

Dieser Text ist behördlich genehmigt.

10-1-2019

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Published on: Wed, 09 Jan 2019 The food enzyme alpha‐amylase (4‐α‐d‐glucan glucanohydrolase; EC 3.2.1.1) is produced with a genetically modified strain of Trichoderma reesei by Danisco US Inc. The genetic modifications do not give rise to safety concerns. The food enzyme is free from viable cells of the production organism and recombinant DNA. This α‐amylase is intended to be used in distilled alcohol production and brewing processes. Residual amounts of total organic solids (TOS) are removed by distill...

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Ampi-Kur ad us. vet., Eutersuspension

Ampi-Kur ad us. vet., Eutersuspension

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Institut für Veterinärpharmakologie und toxikologie

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Versican Plus DHPPi/L4 ad us. vet.

Versican Plus DHPPi/L4 ad us. vet.

● Änderung Text "Kurzbezeichnung", "Zusammensetzung", "Indikation", "Dosierung / Anwendung", "Anwendungseinschränkungen", "Unerwünschte Wirkungen", "Wechselwirkungen", "Sonstige Hinweise" und "Packungen"

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Versican Plus DHPPi/L4R ad us. vet.

Versican Plus DHPPi/L4R ad us. vet.

● Änderung Text "Zusammensetzung", "Indikation", "Dosierung / Anwendung", "Anwendungseinschränkungen", "Unerwünschte Wirkungen", "Wechselwirkungen", "Sonstige Hinweise" und "Packungen"

Institut für Veterinärpharmakologie und toxikologie

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Versican Plus L4 ad us. vet.

Versican Plus L4 ad us. vet.

● Änderung Text "Eigenschaften", "Dosierung / Anwendung", "Anwendungseinschränkungen", "Unerwünschte Wirkungen", "Wechselwirkungen" und "Sonstige Hinweise"

Institut für Veterinärpharmakologie und toxikologie

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Versican Plus Pi/L4 ad us. vet.

Versican Plus Pi/L4 ad us. vet.

● Änderung Text "Kurzbezeichnung", "Zusammensetzung", "Indikationen", "Dosierung / Anwendung", "Anwendungseinschränkungen", "Unerwünschte Wirkungen" und "Wechselwirkungen"

Institut für Veterinärpharmakologie und toxikologie

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Perlutex ad us. vet., Tabletten

Perlutex ad us. vet., Tabletten

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Institut für Veterinärpharmakologie und toxikologie

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Schauma-Dip ad us. vet., Zitzendesinfektionsmittel

Schauma-Dip ad us. vet., Zitzendesinfektionsmittel

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Bovilis BTV8 ad us. vet.

Bovilis BTV8 ad us. vet.

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12-12-2018

Activyl TickPlus spot-on Hund XS ad us. vet., insektizide Loesung zum Auftragen auf die Haut

Activyl TickPlus spot-on Hund XS ad us. vet., insektizide Loesung zum Auftragen auf die Haut

● Umwandlung in Exportzulassung (Exportspezialität): nur für den Vertrieb im Ausland

Institut für Veterinärpharmakologie und toxikologie

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Activyl TickPlus spot-on Hund S ad us. vet., insektizide Loesung zum Auftragen auf die Haut

Activyl TickPlus spot-on Hund S ad us. vet., insektizide Loesung zum Auftragen auf die Haut

● Umwandlung in Exportzulassung (Exportspezialität): nur für den Vertrieb im Ausland

Institut für Veterinärpharmakologie und toxikologie

12-12-2018

Activyl TickPlus spot-on Hund M ad us. vet., insektizide Loesung zum Auftragen auf die Haut

Activyl TickPlus spot-on Hund M ad us. vet., insektizide Loesung zum Auftragen auf die Haut

● Umwandlung in Exportzulassung (Exportspezialität): nur für den Vertrieb im Ausland

Institut für Veterinärpharmakologie und toxikologie

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Activyl TickPlus spot-on Hund L ad us. vet., insektiztide Loesung zum Auftragen auf die Haut

Activyl TickPlus spot-on Hund L ad us. vet., insektiztide Loesung zum Auftragen auf die Haut

● Umwandlung in Exportzulassung (Exportspezialität): nur für den Vertrieb im Ausland

Institut für Veterinärpharmakologie und toxikologie

12-12-2018

Activyl TickPlus spot-on Hund XL ad us. vet., insektizide Loesung zum Auftragen auf die Haut

Activyl TickPlus spot-on Hund XL ad us. vet., insektizide Loesung zum Auftragen auf die Haut

● Umwandlung in Exportzulassung (Exportspezialität): nur für den Vertrieb im Ausland

Institut für Veterinärpharmakologie und toxikologie

12-12-2018

Carofertin ad us. vet., Injektionsemulsion

Carofertin ad us. vet., Injektionsemulsion

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Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 5 mg ad us. vet., Kautabletten fuer Hunde

Simparica 5 mg ad us. vet., Kautabletten fuer Hunde

● Indikationserweiterung (Demodex canis, Otodectes cynotis) ● Änderung Text "Eigenschaften / Wirkungen", "Indikationen", "Dosierung / Anwendung" und "Unerwünschte Wirkungen"

Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 10 mg ad us. vet., Kautabletten fuer Hunde

Simparica 10 mg ad us. vet., Kautabletten fuer Hunde

● Indikationserweiterung (Demodex canis, Otodectes cynotis) ● Änderung Text "Eigenschaften / Wirkungen", "Indikationen", "Dosierung / Anwendung" und "Unerwünschte Wirkungen"

Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 20 mg ad us. vet., Kautabletten fuer Hunde

Simparica 20 mg ad us. vet., Kautabletten fuer Hunde

● Indikationserweiterung (Demodex canis, Otodectes cynotis) ● Änderung Text "Eigenschaften / Wirkungen", "Indikationen", "Dosierung / Anwendung" und "Unerwünschte Wirkungen"

Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 40 mg ad us. vet., Kautabletten fuer Hunde

Simparica 40 mg ad us. vet., Kautabletten fuer Hunde

● Indikationserweiterung (Demodex canis, Otodectes cynotis) ● Änderung Text "Eigenschaften / Wirkungen", "Indikationen", "Dosierung / Anwendung" und "Unerwünschte Wirkungen"

Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 80 mg ad us. vet., Kautabletten fuer Hunde

Simparica 80 mg ad us. vet., Kautabletten fuer Hunde

● Indikationserweiterung (Demodex canis, Otodectes cynotis) ● Änderung Text "Eigenschaften / Wirkungen", "Indikationen", "Dosierung / Anwendung" und "Unerwünschte Wirkungen"

Institut für Veterinärpharmakologie und toxikologie

11-12-2018

Simparica 120 mg ad us. vet., Kautabletten fuer Hunde

Simparica 120 mg ad us. vet., Kautabletten fuer Hunde

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Zulvac 8 Bovis ad us. vet., Suspension zur Injektion fuer Rinder

Zulvac 8 Bovis ad us. vet., Suspension zur Injektion fuer Rinder

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Hyalovet 20 ad us. vet., Injektionsloesung

Hyalovet 20 ad us. vet., Injektionsloesung

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Milteforan 20 mg/ml ad us. vet., orale Loesung

Milteforan 20 mg/ml ad us. vet., orale Loesung

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Institut für Veterinärpharmakologie und toxikologie

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Ubroseal ad us. vet., intramammaere Suspension

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Arnica compositum ad us. vet., Tabletten

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UpCard ad us. vet. 0,75 mg, teilbare Tabletten

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UpCard ad us. vet. 3 mg, teilbare Tabletten

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Ulcergold ad us. vet., orale Paste

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Feliserin PRC ad us. vet.

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Institut für Veterinärpharmakologie und toxikologie

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Felimazole 2.5 mg ad us. vet., Filmtabletten fuer Katzen

Felimazole 2.5 mg ad us. vet., Filmtabletten fuer Katzen

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Institut für Veterinärpharmakologie und toxikologie

13-11-2018

Felimazole 5 mg ad us. vet., Filmtabletten fuer Katzen

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Institut für Veterinärpharmakologie und toxikologie

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Pyrogenium compositum ad us. vet., fluessige Verduennung

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On 12/12/18 GE Healthcare Recalled CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA has identified this as a Class I Recall, the most serious type recall. Read more about the recall: https://go.usa.gov/

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Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic)

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GE Healthcare Recalls CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA @US has identified this as a Class I Recall, the most serious type recall. Read more about the recall here:  https://go.usa.gov/xE38

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FDA - U.S. Food and Drug Administration

14-12-2018

#ICYMI: @US_FDA cleared a mobile medical app to help those with #opioid use disorder stay in recovery programs. Read more about the clearance here:  https://go.usa.gov/xE3ke  #FDA #MedicalDevice

#ICYMI: @US_FDA cleared a mobile medical app to help those with #opioid use disorder stay in recovery programs. Read more about the clearance here: https://go.usa.gov/xE3ke  #FDA #MedicalDevice

#ICYMI: @US_FDA cleared a mobile medical app to help those with #opioid use disorder stay in recovery programs. Read more about the clearance here: https://go.usa.gov/xE3ke  #FDA #MedicalDevice

FDA - U.S. Food and Drug Administration

14-12-2018


Final Guideline on Active Substance Master File Procedure - Revision 4

Final Guideline on Active Substance Master File Procedure - Revision 4

Final Guideline on Active Substance Master File Procedure - Revision 4

Europe - EMA - European Medicines Agency

10-12-2018

.@US_FDA is emphasizing the importance of manual cleaning prior to disinfection or sterilization and proper servicing of duodenoscopes. Read more:  https://go.usa.gov/xPShF  #MedicalDevice #FDApic.twitter.com/HiJbgPnsPt

.@US_FDA is emphasizing the importance of manual cleaning prior to disinfection or sterilization and proper servicing of duodenoscopes. Read more: https://go.usa.gov/xPShF  #MedicalDevice #FDApic.twitter.com/HiJbgPnsPt

. @US_FDA is emphasizing the importance of manual cleaning prior to disinfection or sterilization and proper servicing of duodenoscopes. Read more: https://go.usa.gov/xPShF  #MedicalDevice #FDA pic.twitter.com/HiJbgPnsPt

FDA - U.S. Food and Drug Administration

1-12-2018

.@US_FDA scientists have replicated an imaging clinical trial using computer methods, suggesting in silico trials hold promise for regulatory evaluation.  https://ja.ma/2rdAtre pic.twitter.com/XiTbPfEkcj

.@US_FDA scientists have replicated an imaging clinical trial using computer methods, suggesting in silico trials hold promise for regulatory evaluation. https://ja.ma/2rdAtre pic.twitter.com/XiTbPfEkcj

. @US_FDA scientists have replicated an imaging clinical trial using computer methods, suggesting in silico trials hold promise for regulatory evaluation. https://ja.ma/2rdAtre  pic.twitter.com/XiTbPfEkcj

FDA - U.S. Food and Drug Administration

30-11-2018

#FDA In Brief: @US_FDA takes steps to advance the safety and accuracy of  blood glucose monitors to empower patients with diabetes with reliable  tools to manage their health. Read more:  https://go.usa.gov/xPMyA   #MedicalDevice

#FDA In Brief: @US_FDA takes steps to advance the safety and accuracy of blood glucose monitors to empower patients with diabetes with reliable tools to manage their health. Read more: https://go.usa.gov/xPMyA  #MedicalDevice

#FDA In Brief: @US_FDA takes steps to advance the safety and accuracy of blood glucose monitors to empower patients with diabetes with reliable tools to manage their health. Read more: https://go.usa.gov/xPMyA  #MedicalDevice

FDA - U.S. Food and Drug Administration

30-11-2018

.@US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall:  https://go.usa.gov/xPMEn  #MedicalDevicepic.twitter.com/YU9Iq

.@US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn  #MedicalDevicepic.twitter.com/YU9Iq

. @US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn  #MedicalDevice pic.twitter.com/YU9Iq3Yw0b

FDA - U.S. Food and Drug Administration

30-11-2018

.@US_FDA issues class I recall, the most serious type pf recall: Zimmer  Biomet, Inc. Recalls Spinal Fusion & Long Bone Stimulators Due to Lack  of Adequate Validation and Controls to Ensure Product Cleanliness. Read  more about the recall:  https://go.us

.@US_FDA issues class I recall, the most serious type pf recall: Zimmer Biomet, Inc. Recalls Spinal Fusion & Long Bone Stimulators Due to Lack of Adequate Validation and Controls to Ensure Product Cleanliness. Read more about the recall: https://go.us

. @US_FDA issues class I recall, the most serious type pf recall: Zimmer Biomet, Inc. Recalls Spinal Fusion & Long Bone Stimulators Due to Lack of Adequate Validation and Controls to Ensure Product Cleanliness. Read more about the recall: https://go.usa.gov/xPMEK  #MedicalDevice pic.twitter.com/M55ddC98wW

FDA - U.S. Food and Drug Administration

30-11-2018

.@US_FDA has selected 8 novel medical devices as participants in #FDA’s Innovation Challenge to address the #OpioidEpidemic by preventing and treating opioid use disorder. #FDAInnovationChallenge

.@US_FDA has selected 8 novel medical devices as participants in #FDA’s Innovation Challenge to address the #OpioidEpidemic by preventing and treating opioid use disorder. #FDAInnovationChallenge

. @US_FDA has selected 8 novel medical devices as participants in #FDA’s Innovation Challenge to address the #OpioidEpidemic by preventing and treating opioid use disorder. #FDAInnovationChallenge

FDA - U.S. Food and Drug Administration

26-11-2018

#DYK November is #NationalHealthySkinMonth. Are you thinking about getting Dermal Fillers? Check out the @US_FDA's information on Dermal Fillers before you do:  https://go.usa.gov/xPHtk   #FDA #MedicalDevice

#DYK November is #NationalHealthySkinMonth. Are you thinking about getting Dermal Fillers? Check out the @US_FDA's information on Dermal Fillers before you do: https://go.usa.gov/xPHtk  #FDA #MedicalDevice

#DYK November is #NationalHealthySkinMonth. Are you thinking about getting Dermal Fillers? Check out the @US_FDA's information on Dermal Fillers before you do: https://go.usa.gov/xPHtk  #FDA #MedicalDevice

FDA - U.S. Food and Drug Administration

23-11-2018

.@US_FDA issues Class I Medical Device Recall, the most serious type of   recall: Oscor Recalls TB Temporary Bipolar Pacing Leads Due to  Connector Separation Causing Potential for Loss of Pacing. Find out  more:  https://go.usa.gov/xPHxF  #FDA #MedicalDe

.@US_FDA issues Class I Medical Device Recall, the most serious type of recall: Oscor Recalls TB Temporary Bipolar Pacing Leads Due to Connector Separation Causing Potential for Loss of Pacing. Find out more: https://go.usa.gov/xPHxF  #FDA #MedicalDe

. @US_FDA issues Class I Medical Device Recall, the most serious type of recall: Oscor Recalls TB Temporary Bipolar Pacing Leads Due to Connector Separation Causing Potential for Loss of Pacing. Find out more: https://go.usa.gov/xPHxF  #FDA #MedicalDevice pic.twitter.com/negJ6HU4x2

FDA - U.S. Food and Drug Administration

20-11-2018

.@US_FDA issues update to safety communication warning against the use of energy-based devices to perform vaginal “rejuvenation” or vaginal cosmetic procedures. Read more:  https://go.usa.gov/xPAzk  #MedicalDevicepic.twitter.com/pv0k2yaNfj

.@US_FDA issues update to safety communication warning against the use of energy-based devices to perform vaginal “rejuvenation” or vaginal cosmetic procedures. Read more: https://go.usa.gov/xPAzk  #MedicalDevicepic.twitter.com/pv0k2yaNfj

. @US_FDA issues update to safety communication warning against the use of energy-based devices to perform vaginal “rejuvenation” or vaginal cosmetic procedures. Read more: https://go.usa.gov/xPAzk  #MedicalDevice pic.twitter.com/pv0k2yaNfj

FDA - U.S. Food and Drug Administration

20-11-2018

.@US_FDA has updated the webpage on Urogynecologic Surgical Mesh Implants. Read more:  https://go.usa.gov/xPAzD  #MedicalDevice

.@US_FDA has updated the webpage on Urogynecologic Surgical Mesh Implants. Read more: https://go.usa.gov/xPAzD  #MedicalDevice

. @US_FDA has updated the webpage on Urogynecologic Surgical Mesh Implants. Read more: https://go.usa.gov/xPAzD  #MedicalDevice

FDA - U.S. Food and Drug Administration

20-11-2018

.@US_FDA issues Class I Medical Device Recall, the most serious type of recall: Beckman Coulter Life Sciences Beckman Coulter Life Sciences recalls the FC500 Series Flow Cytometers and EPICS XL Series Flow Cytometers. Find out more:  https://go.usa.gov/xP

.@US_FDA issues Class I Medical Device Recall, the most serious type of recall: Beckman Coulter Life Sciences Beckman Coulter Life Sciences recalls the FC500 Series Flow Cytometers and EPICS XL Series Flow Cytometers. Find out more: https://go.usa.gov/xP

. @US_FDA issues Class I Medical Device Recall, the most serious type of recall: Beckman Coulter Life Sciences Beckman Coulter Life Sciences recalls the FC500 Series Flow Cytometers and EPICS XL Series Flow Cytometers. Find out more: https://go.usa.gov/xPAtn  #MedicalDevice #FDA pic.twitter.com/6e064UQ2wg

FDA - U.S. Food and Drug Administration

14-11-2018

The @US_FDA issues a safety communication cautioning doctors & patients of the risks associated w/ using medications that are not approved for use w/ implanted pumps that are delivered into the spinal fluid to treat or   manage pain:  https://go.usa.gov/x

The @US_FDA issues a safety communication cautioning doctors & patients of the risks associated w/ using medications that are not approved for use w/ implanted pumps that are delivered into the spinal fluid to treat or manage pain: https://go.usa.gov/x

The @US_FDA issues a safety communication cautioning doctors & patients of the risks associated w/ using medications that are not approved for use w/ implanted pumps that are delivered into the spinal fluid to treat or manage pain: https://go.usa.gov/xPfuw  #FDA #MedicalDevice pic.twitter.com/kgDSx2PQzn

FDA - U.S. Food and Drug Administration

13-11-2018

#DYK November is #DiabetesAwarenessMonth. As the number of people diagnosed with diabetes continues to grow, @US_FDA  encourages patients and caregivers to beware of illegally markets  diabetes treatments. Check out our Consumer Update on this issue  http

#DYK November is #DiabetesAwarenessMonth. As the number of people diagnosed with diabetes continues to grow, @US_FDA encourages patients and caregivers to beware of illegally markets diabetes treatments. Check out our Consumer Update on this issue http

#DYK November is #DiabetesAwarenessMonth. As the number of people diagnosed with diabetes continues to grow, @US_FDA encourages patients and caregivers to beware of illegally markets diabetes treatments. Check out our Consumer Update on this issue https://go.usa.gov/xPfDx  pic.twitter.com/OGwOusdP1w

FDA - U.S. Food and Drug Administration

8-11-2018

There's only 1 week until the 2018 Patient Engagement Advisory Committee meeting. Join the @US_FDA on Nov 15 to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries.pic.twitter.com/WkDNnXqm

There's only 1 week until the 2018 Patient Engagement Advisory Committee meeting. Join the @US_FDA on Nov 15 to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries.pic.twitter.com/WkDNnXqm

There's only 1 week until the 2018 Patient Engagement Advisory Committee meeting. Join the @US_FDA on Nov 15 to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries. pic.twitter.com/WkDNnXqmbw

FDA - U.S. Food and Drug Administration