Pargenta-50 ad us. vet.

Hauptinformation

  • Handelsname:
  • Pargenta-50 ad us. vet., Injektionslösung
  • Darreichungsform:
  • Injektionslösung
  • 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:
  • Pargenta-50 ad us. vet., Injektionslösung
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Antibiotikum für Wiederkäuer, Pferde, Schweine, Hunde und Katzen

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 46067
  • Letzte Änderung:
  • 02-09-2017

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

Pargenta-50 ad us. vet., Injektionslösung

Dr. E. Graeub AG

Antibiotikum für Wiederkäuer, Pferde, Schweine, Hunde und Katzen

ATCvet: QJ01GB03

Zusammensetzung

1 ml wässerige Injektionslösung enthält:

Gentamicinum (ut G. sulfas) 50 mg

Conserv.: E 216, 0.1 mg E 218, 0.9 mg

Antiox.: E 223, 3.5 mg

Acid. citr.

Dinatr. phosph.

Excip. ad solut. iniect.

Fachinformationen Wirkstoffe (CliniPharm)

Gentamicin

Eigenschaften / Wirkungen

Gentamicin ist ein Aminolgykosid-Antibiotikum, welches erstmals zu Beginn der sechziger

Jahre aus Micromonospora-Arten isoliert worden ist. Gentamicin besitzt ein breites

Wirkungsspektrum. Es umfasst Staphylokokken, Streptokokken, gram-negative Kokken,

gram-positive Stäbchen wie Listerien, Corynebakterien und Clostridien, gram-negative

Stäbchen wie Pseudomonas, Proteus, E. coli und Salmonellen. Gentamicin wirkt sowohl

auf ruhende, als auch auf proliferierende Keime, indem es in die Bakterien eindringt und

an den Ribosomen die Proteinsynthese stört. Es wirkt bakterizid und ist daher für schwere

Infekte und Patienten mit geschwächter Abwehrkraft besonders geeignet. In vitro werden

minimale Hemmstoffkonzentrationen (MHK) von unter 1 µg/ml gefunden. Als sensibel

gelten Erreger mit einer MHK von <5 µg/ml. Bakterizid wirksame Konzentrationen werden

bereits mit der zwei- bis dreifachen MHK erreicht. Niedrigere (nicht mehr bakterizide)

Konzentrationen wirken noch bakteriostatisch.

Die Resistenzbildung erfolgt relativ langsam und ist plasmidgebunden.

Gentamicinresistente Keime sind auch gegen Kanamycin und Neomycin resistent, meist

jedoch nicht umgekehrt.

Pharmakokinetik

Pargenta-Injektionslösung wird nach intramuskulärer oder subkutaner Verabreichung

rasch resorbiert und verteilt. Maximale Serumkonzentrationen werden bereits 30 -

60 Minuten nach der Applikation erreicht. Die Verteilung erstreckt sich über den

extrazellulären Raum und umfasst unter anderem die Synovialflüssigkeit, das

Bronchialsekret und den weiblichen Geschlechtsapparat (Ovarien, Endometrium,

Myometrium, Vaginalgewebe). Bei trächtigen Tieren tritt der Wirkstoff auch in den

Fetalkreislauf über. Im Plasma wird Gentamicin kaum an Proteine gebunden.

Hauptausscheidungsorgane sind die Nieren. Gentamicin wird unverändert und damit in

antibakteriell wirksamer Form im Harn ausgeschieden. Es findet eine tubuläre

Rückresorption statt (20 - 40%), weshalb gute Therapieresultate bei Pyelonephritis zu

erreichen sind. Pargenta-Injektionslösung ist gut wasserlöslich.

Indikationen

Therapie und Prophylaxe von Infektionskrankheiten bei Pferd, Rind, Kalb, Schaf, Ziege,

Schwein, Hund und Katze. Eine besonders gute Wirkung kann erwartet werden gegen die

Keime Bacillus, E. coli, Enterobacter, Enterokokken, Klebsiellen, Pasteurellen, Proteus,

Pseudomonaden, Salmonellen und Staphylokokken. Mit einer weniger guten Wirkung

muss gerechnet werden gegen Streptokokken. Pargenta ist vor allem bei folgenden

Krankheiten angezeigt: Atmungstrakt (im Bronchialsekret werden beachtliche

Konzentrationen erreicht): Bronchitis, Bronchopneumonie, Pneumonie, Tracheitis,

Katzenschnupfen, Zwingerhusten. Harntrakt (hohe Konzentrationen, da Ausscheidung

über den Harn): Cystitis, Nephritis, Pyelonephritis. Haut: eitrige Dermatitis, v.a. verursacht

durch Penicillin-resistente Staphylokokken; Genitaltrakt (beachtliche Konzentrationen in

den Genitalschleimhäuten): Endometritis, Metritis, Pyometra, Vaginitis, Prostatitis,

Prostataabszesse; Körperhöhlen (ausreichende Konzentrationen): Pleuritis, Pericarditis,

Peritonitis; Verdauungstrakt: Gastro-Enteritis, Tonsillitis.

Richtdosis:

Initialdosis:

4 mg/kg

Erhaltungsdosis:

2 mg/kg

Erstbehandlung:

Pferd, Rind:

8 ml/100 kg

Kalb:

4 ml/ 50 kg KGW

Schaf, Ziege:2 ml/ 25 kg KGW

Schwein:

4 ml/ 50 kg KGW

Hund, Katze: 2 ml/ 25 kg KGW

Nachbehandlung:

in 12-stündigen Abständen mit jeweils der halben Dosis.

Pferd:

langsam i.v.

Rind, Kalb:

i.m./s.k./langsam

i.v.

Schaf, Ziege, Schwein,

Hund, Katze:

i.m./s.k

Anwendungseinschränkungen

Kontraindikationen:

Nicht anwenden bei Tieren mit Nierenfunktionsstörungen oder Störungen des Gehör- oder

Gleichgewichtssinnes.

Vorsichtsmassnahmen:

Gentamicin tritt in den Fetalkreislauf über, weshalb die Anwendung am trächtigen Tier

strengste Indikationsstellung erfordert.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Werden bei Tieren nur nach überhöhter Dosierung oder bei renaler Dysfunktion

beobachtet. Bei länger dauernder Anwendung können Störungen des Gehör- und

Gleichgewichtssinnes oder der Nierenfunktion vorkommen.

Rind, Schaf, Ziege:

Milch:3 Tage.

Pferd, Rind, Schaf, Ziege, Schwein:

Muskulatur, Leber

7 Tage.

Nieren:

45 Tage.

Injektionsstelle:

14 Tage.

Wechselwirkungen

Gleichzeitige Verabreichung von Diuretika (wie Furosemid) und potentiell

nephrotoxischen Substanzen vermeiden.

Bei gleichzeitiger Anwendung von Anästhetika können neuromuskuläre Blockaden

auftreten.

Sonstige Hinweise

-Bei Raumtemperatur (15 - 25 °C) lagern.

-Vor Licht geschützt lagern.

Das Präparat darf nur bis zu dem auf der Packung mit "Exp." bezeichneten Datum

verwendet werden.

-Aufbrauchfrist nach erster Entnahme: 28 Tage.

Packungen

Durchstechflaschen zu 100 ml.

Abgabekategorie: A

Hersteller

Dr. E. Gräub AG, Bern

Swissmedic Nr. 46'067

Informationsstand: 07/2003

Dieser Text ist behördlich genehmigt.

6-12-2018

Tris Pharma Issues Voluntary Nationwide Recall of Infants’ Ibuprofen Concentrated Oral Suspension, USP (NSAID) 50 mg per 1.25 mL, Due to Potential Higher Concentrations of Ibuprofen

Tris Pharma Issues Voluntary Nationwide Recall of Infants’ Ibuprofen Concentrated Oral Suspension, USP (NSAID) 50 mg per 1.25 mL, Due to Potential Higher Concentrations of Ibuprofen

Tris Pharma, Inc. has voluntarily recalled three (3) lots of Infants’ Ibuprofen Concentrated Oral Suspension, USP (NSAID) 50 mg per 1.25 mL, to the retail level. The recalled lots of the product have been found to potentially have higher concentrations of ibuprofen.

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Hyalovet 20 ad us. vet., Injektionsloesung

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Institut für Veterinärpharmakologie und toxikologie

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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

6-12-2018

Ubroseal ad us. vet., intramammaere Suspension

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4-12-2018

Arnica compositum ad us. vet., Tabletten

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Institut für Veterinärpharmakologie und toxikologie

29-11-2018

ANSES Newsletter in English - N°50 - November 2018

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France - Agence Nationale du Médicament Vétérinaire

23-11-2018

Semintra 10 mg/ml ad us. vet., orale Loesung

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● Die Neuzulassung erfolgte am 23.11.2018.

Institut für Veterinärpharmakologie und toxikologie

23-11-2018

Duvaxyn WNV ad us. vet.

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● Änderung Packungsgrösse: Karton mit 2 Einwegspritzen

Institut für Veterinärpharmakologie und toxikologie

23-11-2018

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

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● Die Neuzulassung erfolgte am 23.11.2018.

Institut für Veterinärpharmakologie und toxikologie

23-11-2018

UpCard ad us. vet. 3 mg, teilbare Tabletten

UpCard ad us. vet. 3 mg, teilbare Tabletten

● Die Neuzulassung erfolgte am 23.11.2018.

Institut für Veterinärpharmakologie und toxikologie

23-11-2018

UpCard ad us. vet. 7,5 mg, teilbare Tabletten

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● Die Neuzulassung erfolgte am 23.11.2018.

Institut für Veterinärpharmakologie und toxikologie

22-11-2018

Safety and efficacy of Monteban® G100 (narasin) for ducks for fattening

Safety and efficacy of Monteban® G100 (narasin) for ducks for fattening

Published on: Wed, 21 Nov 2018 Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety and efficacy of Monteban® G100 for ducks. Monteban® G100, containing narasin, is intended for the prevention of coccidiosis in ducks for fattening at a dose range of 60–70 mg/kg of complete feed. Narasin from Monteban® G100 is safe for ducks for fattening at a level of 70 mg/kg complete feed...

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Europe - EFSA - European Food Safety Authority Publications

21-11-2018

Safety and efficacy of Monteban® G100 (narasin) for chickens for fattening

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Published on: Tue, 20 Nov 2018 The feed additive Monteban® G100, containing the active substance narasin, an ionophore anticoccidial, is intended to control coccidiosis in chickens for fattening at a dose of 60–70 mg/kg complete feed. Narasin is produced by fermentation. Limited data on the taxonomic identification of the production strain did not allow the proper identification of strain NRRL 8092 as Streptomyces aureofaciens. The FEEDAP Panel cannot conclude on the absence of genetic determinants for ...

Europe - EFSA - European Food Safety Authority Publications

21-11-2018

Metacam 0,5 mg/ml ad us. vet., orale Suspension

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● Neue Zieltierart: Meerschweinchen ● Änderung Präparatename, früher: Metacam® 0,5 mg/ml Katzen ad us. vet., orale Suspension ● Änderung Text "Zusammensetzung", "Pharmakokinetik", "Indikationen", "Dosierung / Anwendung", "Anwendungseinschränkungen", "Unerwünschte Wirkungen", "Wechselwirkungen" und "Sonstige Hinweise"

Institut für Veterinärpharmakologie und toxikologie

21-11-2018

Ulcergold ad us. vet., orale Paste

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● Die Neuzulassung erfolgte am 21.11.2018.

Institut für Veterinärpharmakologie und toxikologie

19-11-2018

Certain Option and Personelle sunscreens voluntarily recalled because of bacterial contamination

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One lot each of Option Family Sunscreen Lotion SPF 50 and Personnelle Sport Sunscreen Lotion SPF 50 have been voluntarily recalled by Empack Spraytech Inc. because of bacterial contamination.

Health Canada

15-11-2018

Safety and efficacy of Monimax® (monensin sodium and nicarbazin) for chickens for fattening and chickens reared for laying

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Europe - EFSA - European Food Safety Authority Publications

15-11-2018

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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Institut für Veterinärpharmakologie und toxikologie

13-11-2018

Felimazole 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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Pyrogenium compositum ad us. vet., fluessige Verduennung

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Institut für Veterinärpharmakologie und toxikologie

10-11-2018

Pest categorisation of Popillia japonica

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Institut für Veterinärpharmakologie und toxikologie

6-11-2018

Levamisol 100 mg/ml ad us. vet., Injektionsloesung

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Institut für Veterinärpharmakologie und toxikologie

6-11-2018

Suanovil 20 ad us. vet., Injektionsloesung

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Institut für Veterinärpharmakologie und toxikologie

14-12-2018

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

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FDA - U.S. Food and Drug Administration

14-12-2018

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11-12-2018

REYATAZ® 50 mg Pulver zum Einnehmen

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10-12-2018

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FDA - U.S. Food and Drug Administration

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Syneudon® 50 mg

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7-12-2018

Benepali® 50 mg

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7-12-2018

Diabact UBT 50 mg Tabletten

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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

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FDA - U.S. Food and Drug Administration

30-11-2018

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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

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. @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

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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

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FDA - U.S. Food and Drug Administration

28-11-2018

Xadago 50 mg / 100 mg Filmtabletten

Rote - Liste

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

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FDA - U.S. Food and Drug Administration

26-11-2018

Today, #FDA’s device center also posted performance report highlighting measures taken to increase predictability, transparency of 510(k) review process, incl. 50 final guidance documents on important medical device policy issues issued since 2009.  https

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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

Amiodaron-hameln 50 mg/ml

Rote - Liste

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

19-11-2018

Leponex® 50 mg

Rote - Liste

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

6-11-2018

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