Super Mastitar ad us. vet.

Hauptinformation

  • Handelsname:
  • Super Mastitar® ad us. vet., Suspension
  • Darreichungsform:
  • Suspension
  • 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:
  • Super Mastitar® ad us. vet., Suspension
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Suspension zur intramammären Anwendung; Antibiotika-Kombination zum Trockenstellen von Kühen

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 42340
  • Letzte Änderung:
  • 02-09-2017

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

Super Mastitar

ad us. vet., Suspension

MSD Animal Health GmbH

Suspension zur intramammären Anwendung; Antibiotika-Kombination zum

Trockenstellen von Kühen

ATCvet: QJ51RC23

Zusammensetzung

Wirkstoffe: Benzylpenicillinum procainum 1 Mio U.I., Benzylpenicillinum kalicum

500'000 U.I., Neomycinum (ut Neomycini sulfas) 500 mg

-Hilfsstoffe: Aluminii tristearas, Paraffinum liquidum ad susp. oleos. pro vase 9 g

-galenische Form: ölige Suspension zur intramammären Anwendung

1 Reinigungstuch mit 2.4 ml Lösung enthält 70% Isopropylalkohol und 30% gereinigtes

Wasser

Fachinformationen Wirkstoffe (CliniPharm)

Benzylpenicillin - Neomycin - Penicillin G-Procain

Eigenschaften / Wirkungen

Benzylpenicillin ist wirksam gegen Gelbgalt- und die meisten anderen Euterstreptokokken

sowie gegen Staphylokokken, die keine Penicillinase bilden. Neomycin wirkt v.a. gegen

gramnegative Bakterien wie E. coli und Klebsiella spp., aber auch gegen Penicillin-

resistente Staphylokokken. Das Wirkungsspektrum der beiden Antibiotika deckt alle

üblichen Mastitis-Erreger ab. β-Laktam-Antibiotika wirken bakterizid durch Hemmung der

Synthese von Peptidoglykanen; Aminoglykoside sind für empfindliche Organismen

bakterizid durch irreversible Hemmung der Proteinsynthese.

Pharmakokinetik

Die Resorption vom Euter ins Blut ist niedrig nach intramammärer Verabreichung. Die

höchsten Konzentrationen von Penicillin und Neomycin im Serum von Kühen werden

24 Stunden nach intramammärer Infusion des Präparates erreicht. Penicillin und

Neomycin werden vorwiegend über den Urin ausgeschieden. Die höchsten

Konzentrationen im Urin werden für Penicillin einen Tag und für Neomycin 9 Tage nach

der Verabreichung gemessen.

Benzylpenicillin Kalium erreicht rasch hohe Initialspiegel im Euter, während mit

Benzylpenicillin Procain lange anhaltende Penicillin-Spiegel erzielt werden. Die höchste

Penicillin-Konzentration im Eutersekret wird 1 Woche nach Verabreichung gemessen,

danach fällt die Konzentration innerhalb von 6 Wochen nach Verabreichung kontinuierlich

bis unter die Nachweisgrenze von Penicillin.

Die höchsten Konzentrationen von Neomycin im Eutersekret werden 1 - 3 Wochen nach

der Verabreichung gemessen und fallen dann bis zum Ende der Trockenstehzeit ab.

Jedoch bleibt die Neomycin-Konzentration während der gesamten Trockenstehzeit im

wirksamen Bereich.

In Plasma und Urin, die nach einer normal langen Trockenstehzeit gewonnen werden,

kann weder Penicillin noch Neomycin festgestellt werden.

Indikationen

Super Mastitar

ist indiziert zur Behandlung von subklinischen Mastitiden bei

trockenstehenden Kühen sowie zur Vorbeugung von Neuinfektionen während der

Trockenzeit, die durch empfindliche Keime verursacht werden.

Dosierung / Anwendung

1 Injektor/Viertel intramammär.

Vor der Applikation wird das Euter gründlich ausgemolken, die Zitzenkuppen werden

gereinigt und mit beiliegendem Zitzenreinigungstuch desinfiziert. Danach wird, ohne die

Injektorspitze mit den Fingern zu berühren, in jedes Viertel 1 Injektor instilliert.

Anwendungseinschränkungen

Kontraindikationen

Nicht bei laktierenden Kühen anwenden.

Nicht anwenden bei Tieren mit bekannter Überempfindlichkeit gegen Penicillin oder

Aminoglykoside. `

Beiliegendes Reinigungstuch nicht bei Läsionen der Zitzenhaut verwenden.

Vorsichtsmassnahmen

lnjektor nur zum einmaligen Gebrauch. Jegliche Kontamination der Injektorspitze ist zu

vermeiden.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Bei einigen Tieren sind allergische Reaktionen vom Soforttyp beschrieben worden, die mit

Agitation, Zittern, Euteroedem sowie erhöhter Körpertemperatur einhergehen können.

Essbare Gewebe

28 Tage

Milch:

2.5 Tage (5 Gemelke) bei einer Trockenstehzeit von ≥ 35 Tagen

Bei einer Trockenstehzeit von < 35 Tagen sollte die Milch vor

Ablieferung auf Hemmstoffe untersucht werden.

Wechselwirkungen

Aminoglykoside und β-Laktam-Antibiotika können synergistisch wirken.

Die gleichzeitige Anwendung bakteriostatischer Wirkstoffe kann die Wirkung von Penicillin

antagonisieren.

Sonstige Hinweise

Bei Raumtemperatur (15 - 25°C) lagern.

Arzneimittel, für Kinder unerreichbar aufbewahren.

Packungen

Packung mit 4 Injektoren à 9 g und 4 Reinigungstüchern

Packung mit 20 Injektoren à 9 g und 20 Reinigungstüchern

Abgabekategorie: A

Swissmedic Nr. 42'340

Informationsstand: 03/2010

Dieser Text ist behördlich genehmigt.

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Versican Plus DHPPi/L4R ad us. vet.

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

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Versican Plus L4 ad us. vet.

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

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Versican Plus Pi/L4 ad us. vet.

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Perlutex ad us. vet., Tabletten

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

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Institut für Veterinärpharmakologie und toxikologie

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

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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

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

Institut für Veterinärpharmakologie und toxikologie

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

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

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

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Institut für Veterinärpharmakologie und toxikologie

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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

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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

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

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

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Institut für Veterinärpharmakologie und toxikologie

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Institut für Veterinärpharmakologie und toxikologie

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UpCard ad us. vet. 3 mg, teilbare Tabletten

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Institut für Veterinärpharmakologie und toxikologie

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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

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● Änderung Text "Anwendungseinschränkungen", "Wechselwirkungen" und "Sonstige Hinweise"

Institut für Veterinärpharmakologie und toxikologie

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

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

● Änderung Text "Anwendungseinschränkungen", "Wechselwirkungen" und "Sonstige Hinweise"

Institut für Veterinärpharmakologie und toxikologie

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Pyrogenium compositum ad us. vet., fluessige Verduennung

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Institut für Veterinärpharmakologie und toxikologie

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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

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

21-11-2018

EU/3/18/2087 (Consejo Superior de Investigaciones Cientificas (CSIC))

EU/3/18/2087 (Consejo Superior de Investigaciones Cientificas (CSIC))

EU/3/18/2087 (Active substance: Etamsylate) - Orphan designation - Commission Decision (2018)7796 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/135/18

Europe -DG Health and Food Safety

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