Anapen 500 Mikrogramm

Hauptinformation

  • Handelsname:
  • Anapen 500 Mikrogramm Injektionslösung
  • Darreichungsform:
  • Injektionslösung
  • Zusammensetzung:
  • adrenalinum 0.500 mg, natrii chloridum, antiox.: E 223 0.510 mg, Wasser iniectabilia für dosi.
  • Verwenden für:
  • Menschen
  • Art der Medizin:
  • Biologische Medizin

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:
  • Anapen 500 Mikrogramm Injektionslösung
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Synthetika
  • Therapiebereich:
  • Notfallmässige Behandlung von Allergien und Anaphylaxien

Weitere Informationen

Status

  • Quelle:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Zulassungsnummer:
  • 57570
  • Berechtigungsdatum:
  • 25-05-2007
  • Letzte Änderung:
  • 25-10-2018

21-11-2018

Setting of an import tolerance for mandipropamid in cocoa beans

Setting of an import tolerance for mandipropamid in cocoa beans

Published on: Tue, 20 Nov 2018 In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Syngenta Agro GmbH submitted a request to the competent national authority in Austria to set a maximum residue level (MRL) for the active substance mandipropamid in cocoa beans imported from Nigeria and Cameroon. The data submitted in support of the request were found to be sufficient to derive a MRL proposal of 0.06 mg/kg. Adequate analytical methods for enforcement are available to control the res...

Europe - EFSA - European Food Safety Authority Publications

31-10-2018

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

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

Published on: Tue, 30 Oct 2018 00:00:00 +0100 The product Bergazym® P100 contains a xylanase which is produced by a non‐genetically modified strain of Trichoderma reesei. The additive is available in a coated granular form and it is intended to be used as a zootechnical additive (functional group: digestibility enhancers) for chickens for fattening, and weaned piglets at the dose of 1,500 EPU/kg feed. The production strain and the additive were fully characterised in a previous assessment of the Panel o...

Europe - EFSA - European Food Safety Authority Publications

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

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

Published on: Tue, 23 Oct 2018 00:00:00 +0200 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 HOSTAZYM® X as a feed additive for sows in order to have benefit in piglets. The additive HOSTAZYM® X contains endo‐1,4‐beta‐xylanase and is available in liquid and solid formulations. This product is authorised as a feed additive for chickens for fattening, tu...

Europe - EFSA - European Food Safety Authority Publications

1-10-2018

Public Notification: FX75000 contains hidden drug ingredient

Public Notification: FX75000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use FX75000, a product promoted for sexual enhancement. This product was identified during an examination of international mail shipments.

FDA - U.S. Food and Drug Administration

20-9-2018

Euthoxin 500 mg/ml ad us. vet., Injektionsloesung

Euthoxin 500 mg/ml ad us. vet., Injektionsloesung

● Die Neuzulassung erfolgte am 20.09.2018.

Institut für Veterinärpharmakologie und toxikologie

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

13-11-2018

Nplate® 125/250/500 Mikrogramm Pulver

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13-11-2018

Relifex® 500 mg Filmtabletten

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13-11-2018

CEPROTIN 500 I.E.

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12-11-2018

Erythrocin®-i.v. 500 mg/1,0 g

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12-11-2018

Erythrocin 500 mg Neo

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9-11-2018

Claversal® 500 mg Tabletten

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6-11-2018

Tetracyclin Wolff® 500 mg

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6-11-2018

Arilin® 500 mg

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1-11-2018

Ovitrelle 250 Mikrogramm/0,5 ml

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30-10-2018

AGGRASTAT 250 Mikrogramm/ml Konzentrat

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23-10-2018

Feanolla® 75 Mikrogramm Filmtabletten

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23-10-2018

Calciumacetat-Nefro® 500 mg/700 mg

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22-10-2018

BeneFIX® 250/500/1000/2000/3000 I.E.

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25-9-2018

Rebif 44 Mikrogramm/0,5 ml (Patrone)

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25-9-2018

Rebif 22 Mikrogramm/0,5 ml (Patrone)

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14-9-2018

Fentanyl AWD® Matrix 12 Mikrogramm/h

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7-9-2018

Aloxi® 500 Mikrogramm Weichkapseln

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7-9-2018

Dexdor 100 Mikrogramm/ml

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