Lopatol 100 ad us. vet.[A]

Hauptinformation

  • Handelsname:
  • Lopatol® 100 ad us. vet.[A], Lacktabletten
  • Darreichungsform:
  • Lacktabletten
  • 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:
  • Lopatol® 100 ad us. vet.[A], Lacktabletten
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Orales Breitband-Anthelminthikum für Hunde

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 43664
  • Letzte Änderung:
  • 03-11-2018

Packungsbeilage

Lopatol

100 ad us. vet.

, Lacktabletten

Elanco Tiergesundheit AG

HINWEIS: derzeit nicht erhältlich (Ausverkauft / Nicht lieferbar)!

Orales Breitband-Anthelminthikum für Hunde

ATCvet: QP52AX01

Zusammensetzung

Lopatol 100 enthält 100 mg Nitroscanat pro Lacktablette

Excipiens pro praeparatione (compresso obducto)

Lacktabletten

Fachinformationen Wirkstoffe (CliniPharm)

Nitroscanat

Eigenschaften / Wirkungen

Lopatol ist ein hochwirksames Breitband-Anthelminthikum für Welpen und

ausgewachsene Hunde. In den Lacktabletten liegt der Wirkstoff Nitroscanat in besonders

fein verteilter Form vor, wodurch ein optimaler anthelminthischer Wirkungsgrad erreicht

wird. Dadurch kann die Standard-Dosierung entsprechend niedrig gehalten werden. Das

Wirkungsspektrum umfasst die wichtigen beim Hund auftretenden intestinalen Würmer

(reife und unreife Stadien):

Spulwürmer:

Toxocara canis, Toxascaris leonina

Hakenwürmer:

Ancylostoma caninum, Ancylostoma braziliense, Uncinaria stenocephala

Bandwürmer:

Dipylidium caninum, Echinococcus granulosus, Spirometra erinacei,

Taenia pisiformis, Taenia hydatigena, Taenia ovis

Andere Spezies:Strongyloides stercoralis

Pharmakokinetik

Nitroscanat wird nach oraler Verabreichung im Darm resorbiert. Es erreicht maximale

Plasmaspiegel nach 24 Stunden. Die Verabreichung von Nitroscanat mit dem Futter, wie

empfohlen, führt gegenüber der Gabe an nüchterne Hunde zu einer viel besseren

Resorption des Wirkstoffs (C

[maximale Blutkonzentration] und AUC [Fläche unter der

Blutkonzentration/Zeit-Kurve]). Nitroscanat wird zum grössten Teil rasch im Urin und Kot

ausgeschieden. Das restliche an Protein gebundene Nitroscanat wird langsamer eliminiert.

Indikationen

Befall mit Spulwürmern, Hakenwürmern, Strongyloides, Dipylidium, Echinococcus und

Taenien.

Spulwürmer, Hakenwürmer, Strongyloides, Dipylidium und Taenien:

50 mg Nitroscanat/kg Körpergewicht

= 1 Tablette zu 100 mg/2 kg Körpergewicht

= 1 Tablette zu 500 mg/10 kg Körpergewicht

Gewicht des

Hundes in kg

Anzahl Tabletten

Lopatol 100

Anzahl Tabletten

Lopatol 500

1 - 2

3 - 4

5 - 6

7 - 10

11 - 20

21 - 30

31 - 40

Echinococcus:

100 mg Nitroscanat/kg Körpergewicht

= 1 Tablette zu 100 mg/1 kg Körpergewicht

= 1 Tablette zu 500 mg/5 kg Körpergewicht

mit Wiederholung im Abstand von 48 Stunden.

Lopatol morgens dem nüchternen Hund mit ca. ¼ der täglichen Futterration verabreichen.

Den restlichen Teil der Futterration abends geben. Es soll genügend Trinkwasser zur

Verfügung stehen. Lopatol kann auch in etwas Wasser aufgeschlämmt und so dem Futter

beigemischt werden.

Behandlungsplan

WELPEN: sollen wegen der Reinfektionsgefahr im Alter von 2, 4, 6 und 8 Wochen, und

danach im ersten Jahr 3 - 4 Mal entwurmt werden.

ERWACHSENE HUNDE: Entwurmung 1 - 2 Mal pro Jahr, oder gemäss Verordnung des

Tierarztes.

ZUCHTHÜNDINNEN: Während der Läufigkeit sowie 2 Wochen vor und 2 Wochen nach

dem Werfen (zusammen mit den Welpen).

HUNDEZUCHTEN: wegen der erhöhten Reinfektionsgefahr empfiehlt es sich, alle Hunde

in Zuchten 4 - 6 Mal jährlich einer Wurmkur zu unterziehen.

Nach positivem Befund einer parasitologischen Kotuntersuchung soll immer eine

Behandlung erfolgen. Bei Befall mit Spulwürmern muss die Behandlung nach 2 Wochen

wiederhohlt werden. Bei Dipylidienbefall wird die Durchführung eines

Flohbekämpfungsprogramms empfohlen.

Anwendungseinschränkungen

Kontraindikationen:

Keine bekannt.

Vorsichtsmassnahmen:

Keine.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Bei Einhaltung der Verabreichungsempfehlung sind Nebenwirkungen wie z.B. Erbrechen

praktisch auszuschliessen.

Wechselwirkungen

Keine bekannt.

Sonstige Hinweise

Vor Wärme schützen (nicht oberhalb 30°C lagern). Tierarzneimittel, für Kinder

unzugänglich aufbewahren. Das Medikament darf nur bis zu dem auf dem Behälter mit

"EXP" bezeichneten Datum verwendet werden.

Packungen

Packung mit 24 Schachteln à 6 Tabletten à 100 mg Nitroscanat

Nicht erhältlich: Ausverkauft / Nicht lieferbar!

Abgabekategorie: B

Swissmedic Nr. 43'664

Informationsstand: 06/2005

Dieser Text ist behördlich genehmigt.

15-11-2018

Feliserin PRC ad us. vet.

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● Änderung Text gesamte Arzneimittelinformation

Institut für Veterinärpharmakologie und toxikologie

13-11-2018

Alebrije Dist Wholesale Recalls Quesillo Queseria “La Milagrosa” and “Alebrije Cheese” Because of Possible Health Risk

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FDA - U.S. Food and Drug Administration

13-11-2018

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

13-11-2018

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

13-11-2018

Pyrogenium compositum ad us. vet., fluessige Verduennung

Pyrogenium compositum ad us. vet., fluessige Verduennung

● Änderung Präparatenamen sowie Text "Zusammensetzung", "Indikationen", "Anwendungseinschränkungen", "Sonstige Hinweise" und "Packungen"

Institut für Veterinärpharmakologie und toxikologie

10-11-2018

Pest categorisation of Popillia japonica

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Published on: Thu, 08 Nov 2018 00:00:00 +0100 The Panel on Plant Health performed a pest categorisation of Popillia japonica(Coleoptera: Scarabaeidae) for the EU. P. japonica is a distinguishable species listed in Annex IAII of Council Directive 2000/29/EC. It is native to Japan but established in the USA in the early 20th century. It spreads from New Jersey to most US states east of the Mississippi, some to the west and north into Canada. P. japonica feeds on over 700 plant species. Adults attack folia...

Europe - EFSA - European Food Safety Authority Publications

9-11-2018

Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient (API)

Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient (API)

Sandoz Inc. is voluntarily recalling one lot of Losartan Potassium Hydrochlorothiazide Tablets, USP 100mg/25mg to the consumer level. This product is being recalled due to the trace amount of an impurity, N-nitrosodiethylamine (NDEA) contained in the API Losartan, USP manufactured by Zhejiang Huahai Pharmaceutical Co. Ltd. Sandoz Inc. Losartan Potassium Hydrochlorothiazide product is manufactured by Lek Pharmaceuticals dd, Ljubljana, Slovenia. This impurity, which is a substance that occurs naturally in ...

FDA - U.S. Food and Drug Administration

9-11-2018

First Choice Vapor recalls Unflavoured 100 mg Nicotine Base E-Liquids

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These vaping products do not meet requirements of the Consumer Chemicals and Containers Regulations, 2001 (CCCR, 2001) under the Canada Consumer Product Safety Act.

Health Canada

9-11-2018

Safety assessment of the substance Ln 1,4‐benzene dicarboxylic acid (with Ln = La, Eu, Gd, Tb) for use in food contact materials

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Published on: Wed, 07 Nov 2018 00:00:00 +0100 The EFSA Panel on Food Contact Materials, Enzymes and Processing Aids (CEP Panel) assessed the safety of the additive Ln 1,4‐benzene dicarboxylic acid (with Ln = La, Eu, Gd, Tb) for use in food contact materials. It is a family of mixtures combining the four lanthanides lanthanum (La), europium (Eu), gadolinium (Gd) and/or terbium (Tb) in different proportions as their 1,4‐benzene dicarboxylate complexes, used as a taggant in plastics for authentication and ...

Europe - EFSA - European Food Safety Authority Publications

8-11-2018

Marbonor 10% ad us. vet., Injektionsloesung

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● Die Neuzulassung erfolgte am 08.11.2018.

Institut für Veterinärpharmakologie und toxikologie

6-11-2018

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

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● Die Neuzulassung erfolgte am 06.11.2018.

Institut für Veterinärpharmakologie und toxikologie

6-11-2018

Suanovil 20 ad us. vet., Injektionsloesung

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

Institut für Veterinärpharmakologie und toxikologie

5-11-2018

Effipro Spot On Hunde S ad us. vet., Loesung zum Auftropfen

Effipro Spot On Hunde S ad us. vet., Loesung zum Auftropfen

● Änderung Text "Sonstige Hinweise" und "Packungen"

Institut für Veterinärpharmakologie und toxikologie

5-11-2018

Effipro Spot On Hunde M ad us. vet., Loesung zum Auftropfen

Effipro Spot On Hunde M ad us. vet., Loesung zum Auftropfen

● Änderung Text "Sonstige Hinweise" und "Packungen"

Institut für Veterinärpharmakologie und toxikologie

5-11-2018

Effipro Spot On Hunde L ad us. vet., Loesung zum Auftropfen

Effipro Spot On Hunde L ad us. vet., Loesung zum Auftropfen

● Änderung Text "Sonstige Hinweise" und "Packungen"

Institut für Veterinärpharmakologie und toxikologie

5-11-2018

Effipro Spot On Hunde XL ad us. vet., Loesung zum Auftropfen

Effipro Spot On Hunde XL ad us. vet., Loesung zum Auftropfen

● Änderung Text "Sonstige Hinweise" und "Packungen"

Institut für Veterinärpharmakologie und toxikologie

5-11-2018

Effipro Spot On Katzen ad us. vet., Loesung zum Auftropfen

Effipro Spot On Katzen ad us. vet., Loesung zum Auftropfen

● Änderung Text "Sonstige Hinweise" und "Packungen"

Institut für Veterinärpharmakologie und toxikologie

1-11-2018

Three research projects to increase our knowledge of medicinal cannabis

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Danish Medicines Agency

1-11-2018

Seresto ad us. vet., Halsband fuer Hunde groesser 8 kg

Seresto ad us. vet., Halsband fuer Hunde groesser 8 kg

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

Institut für Veterinärpharmakologie und toxikologie

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Seresto ad us. vet., Halsband fuer Katzen und Hunde kleinergleich 8 kg

Seresto ad us. vet., Halsband fuer Katzen und Hunde kleinergleich 8 kg

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

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Efficacy of Bergazym® P100 (endo‐1,4‐β‐xylanase) as a feed additive for chickens for fattening and weaned piglets

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Onsior 5 mg ad us. vet., schmackhafte Tabletten fuer Hunde

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● Änderung Text "Anwendungseinschränkungen"

Institut für Veterinärpharmakologie und toxikologie

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Onsior 10 mg ad us. vet., schmackhafte Tabletten fuer Hunde

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● Änderung Text "Anwendungseinschränkungen"

Institut für Veterinärpharmakologie und toxikologie

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Onsior 20 mg ad us. vet., schmackhafte Tabletten fuer Hunde

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● Änderung Text "Anwendungseinschränkungen"

Institut für Veterinärpharmakologie und toxikologie

30-10-2018

Onsior 40 mg ad us. vet., schmackhafte Tabletten fuer Hunde

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● Änderung Text "Anwendungseinschränkungen"

Institut für Veterinärpharmakologie und toxikologie

29-10-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on the FDA’s new consideration of labeling for sesame allergies

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FDA - U.S. Food and Drug Administration

24-10-2018

Safety and efficacy of Hostazym® X (endo‐1,4‐beta‐xylanase) as a feed additive for sows in order to have benefit in piglets

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

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● Die Neuzulassung erfolgte am 24.10.2018.

Institut für Veterinärpharmakologie und toxikologie

23-10-2018

Bravecto Plus spot-on Katze L ad us. vet., Loesung zum Auftragen auf die Haut

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Institut für Veterinärpharmakologie und toxikologie

23-10-2018

Bravecto Plus spot-on Katze M ad us. vet., Loesung zum Auftragen auf die Haut

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● Die Neuzulassung erfolgte am 23.10.2018.

Institut für Veterinärpharmakologie und toxikologie

23-10-2018

Bravecto Plus spot-on Katze S ad us. vet., Loesung zum Auftragen auf die Haut

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● Die Neuzulassung erfolgte am 23.10.2018.

Institut für Veterinärpharmakologie und toxikologie

22-10-2018

Leucofeligen FeLV/CRP ad us. vet.

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● Änderung Text "Zusammensetzung", "Eigenschaften/Wirkungen", "Indikationen", "Dosierung/Anwendung" und "Anwendungseinschränkungen"

Institut für Veterinärpharmakologie und toxikologie

22-10-2018

Leucogen ad us. vet.

Leucogen ad us. vet.

● Änderung Text "Zusammensetzung", "Indikationen", "Dosierung/Anwendung", "Anwendungseinschränkungen", "Wechselwirkungen" und "Sonstige Hinweise"

Institut für Veterinärpharmakologie und toxikologie

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

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FDA - U.S. Food and Drug Administration

14-11-2018

DuoPlavin® 75 mg/100 mg Filmtabletten

Rote - Liste

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

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FDA - U.S. Food and Drug Administration

13-11-2018

CEPROTIN 1000 I.E.

Rote - Liste

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

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FDA - U.S. Food and Drug Administration

8-11-2018

Palladon® injekt 2 mg/10 mg/100 mg

Rote - Liste

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

6-11-2018

Symkevi® 100 mg/150 mg Filmtabletten

Rote - Liste

2-11-2018

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

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

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

FDA - U.S. Food and Drug Administration

2-11-2018

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

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

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

FDA - U.S. Food and Drug Administration

2-11-2018

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

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

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

FDA - U.S. Food and Drug Administration

1-11-2018

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

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

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

FDA - U.S. Food and Drug Administration

1-11-2018

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

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

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

FDA - U.S. Food and Drug Administration

31-10-2018

Zodin® Omega-3 1000 mg Weichkapseln

Rote - Liste

30-10-2018

#DYK: Mammograms are still the best tool for breast cancer screening.  Check out @US_FDA’s information on the importance of choosing a certified mammography facility:  https://go.usa.gov/xPPpT  #MedicalDevice #BreastCancerAwarenessMonthpic.twitter.com/YaG

#DYK: Mammograms are still the best tool for breast cancer screening. Check out @US_FDA’s information on the importance of choosing a certified mammography facility: https://go.usa.gov/xPPpT  #MedicalDevice #BreastCancerAwarenessMonthpic.twitter.com/YaG

#DYK: Mammograms are still the best tool for breast cancer screening. Check out @US_FDA’s information on the importance of choosing a certified mammography facility: https://go.usa.gov/xPPpT  #MedicalDevice #BreastCancerAwarenessMonth pic.twitter.com/YaGqeGgrTH

FDA - U.S. Food and Drug Administration

30-10-2018

EU/3/18/2076 (Orphan Europe S.A.R.L.)

EU/3/18/2076 (Orphan Europe S.A.R.L.)

EU/3/18/2076 (Active substance: Glycine, L-alanine, L-arginine, L-aspartic acid, L-cysteine, L-cystine, L-glutamic acid, L-histidine, L-lysine monohydrate, L-methionine, L-phenylalanine, L-proline, L-serine, L-threonine, L-tryptophan, L-tyrosine, taurine) - Orphan designation - Commission Decision (2018)7277 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/100/18

Europe -DG Health and Food Safety

26-10-2018

Men can also be diagnosed with breast cancer. Check out the @US_FDA’s information regarding breast cancer in men, available treatments and counseling options:  https://go.usa.gov/xPPpx  ) #MedicalDevice #BreastCancerAwarenessMonthpic.twitter.com/aZBjgCGsB

Men can also be diagnosed with breast cancer. Check out the @US_FDA’s information regarding breast cancer in men, available treatments and counseling options: https://go.usa.gov/xPPpx  ) #MedicalDevice #BreastCancerAwarenessMonthpic.twitter.com/aZBjgCGsB

Men can also be diagnosed with breast cancer. Check out the @US_FDA’s information regarding breast cancer in men, available treatments and counseling options: https://go.usa.gov/xPPpx  ) #MedicalDevice #BreastCancerAwarenessMonth pic.twitter.com/aZBjgCGsB1

FDA - U.S. Food and Drug Administration

25-10-2018

Vancomycin Lyomark 1000 mg Pulver

Rote - Liste

24-10-2018

It’s #BreastCancerAwarenessMonth and the @US_FDA is reminding patients and caregivers that thermography is not a substitute for mammograms.pic.twitter.com/XGJFHvut4x

It’s #BreastCancerAwarenessMonth and the @US_FDA is reminding patients and caregivers that thermography is not a substitute for mammograms.pic.twitter.com/XGJFHvut4x

It’s #BreastCancerAwarenessMonth and the @US_FDA is reminding patients and caregivers that thermography is not a substitute for mammograms. pic.twitter.com/XGJFHvut4x

FDA - U.S. Food and Drug Administration

24-10-2018

Nebido® 1000 mg Injektionslösung

Rote - Liste

22-10-2018

BeneFIX® 250/500/1000/2000/3000 I.E.

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