Vinorelbin Cancernova 10 mg/1 ml

Hauptinformation

  • Handelsname:
  • Vinorelbin Cancernova 10 mg/1 ml Lösung zur intravenösen Injektion/Infusion
  • Darreichungsform:
  • Lösung zur intravenösen Injektion/Infusion
  • Zusammensetzung:
  • vinorelbinum 10 mg zu vinorelbini tartras (1:2), Wasser ad iniectabilia q.s. zu einer Lösung anstelle von 1 ml.
  • Verwenden für:
  • Menschen
  • Art der Medizin:
  • allopathic Droge

Dokumenten

  • für die Allgemeinheit:
  • 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 das Informationsblatt für die Öffentlichkeit.

  • 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:
  • Vinorelbin Cancernova 10 mg/1 ml Lösung zur intravenösen Injektion/Infusion
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Synthetik menschlichen
  • Therapiebereich:
  • Zytostatikum

Weitere Informationen

Status

  • Quelle:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Zulassungsnummer:
  • 57992
  • Berechtigungsdatum:
  • 09-05-2008
  • Letzte Änderung:
  • 06-02-2018

10-8-2018

Enforcement Report for the Week of July 25, 2018

Enforcement Report for the Week of July 25, 2018

Recently Updated Records for the Week of July 25, 2018 Last Modified Date: Friday, August 10, 2018

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Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

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On 1 October 2010, orphan designation (EU/3/10/796) was granted by the European Commission to XOMA Ireland Ltd, Ireland, for recombinant humanised anti-human interleukin-1 beta monoclonal antibody for the treatment of Behçet’s disease.

Europe - EMA - European Medicines Agency

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FDA - U.S. Food and Drug Administration

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11-7-2018

July 10, 2018: Former Des Moines Pharmacy Technician Sentenced for Illegally Tampering with Fentanyl

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FDA - U.S. Food and Drug Administration

11-7-2018

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Europe -DG Health and Food Safety

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By Aug. 10, all packages and advertisements for “covered” tobacco products (except for cigars and pipe tobacco) and roll-your-own/cigarette tobacco products must have the required nicotine warning statement. https://cards.twitter.com/cards/2m2m96/5xn98 …

FDA - U.S. Food and Drug Administration

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Europe -DG Health and Food Safety

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Zovirax Duo 50 mg/g / 10 mg/ g Creme

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Europe -DG Health and Food Safety

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27-7-2018

EU/3/11/868 (Celgene Europe B.V.)

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Europe -DG Health and Food Safety

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Sempera® Liquid 10 mg/ml

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13-7-2018

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Europe -DG Health and Food Safety

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Europe -DG Health and Food Safety

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Europe -DG Health and Food Safety

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Europe -DG Health and Food Safety

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Europe -DG Health and Food Safety

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Europe -DG Health and Food Safety

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Europe -DG Health and Food Safety

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Europe -DG Health and Food Safety