Glucose 30%

Hauptinformation

  • Handelsname:
  • Glucose 30% Infusionslösung 300 mg/ml
  • Dosierung:
  • 300 mg/ml
  • Darreichungsform:
  • Infusionslösung
  • 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:
  • Glucose 30% Infusionslösung 300 mg/ml
    Belgien
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • infusion fluid

Weitere Informationen

Status

  • Quelle:
  • AFMPS - Agence Fédérale des Médicaments et des Produits de Santé - Belgium
  • Zulassungsnummer:
  • BE-V309145
  • Letzte Änderung:
  • 17-04-2018

Packungsbeilage

Bijsluiter – DE versie

Glucose 30 %

PACKUNGSBEILAGE

GEBRAUCHSINFORMATION

Glucose 30%

1.

NAME UND ANSCHRIFT DES ZULASSUNGSINHABERS UND, WENN

UNTERSCHIEDLICH, DES HERSTELLERS, DER FÜR DIE CHARGENFREIGABE

VERANTWORTLICH IST

Zulassungsinhaber

Eurovet NV / SA

Poorthoevestraat 4

B-3550 Heusden-Zolder

Belgien

Für die Chargenfreigabe verantwortlicher Hersteller:

Eurovet Animal Health B.V.

Handelsweg 25

5531 AE Bladel

Niederlande

2.

BEZEICHNUNG DES TIERARZNEIMITTELS

Glucose 30%, Infusionslösung

3.

WIRKSTOFF(E) UND SONSTIGE BESTANDTEILE

Dextrose (als Monohydrat) 300 mg/ml, konzentrierte Salzsäure und Wasser zur Injektion.

4.

ANWENDUNGSGEBIET(E)

Glukose 30% ist bei Erkrankungen, bei denen ein Energiebedarfsmangel entstanden ist, indiziert.

Zum Beispiel bei: - Acetonämie (Ketose) bei Kühen

- Trächtigkeitstoxämie bei Schafen und Ziegen.

5.

GEGENANZEIGEN

Da es sich hier um eine hypertone Lösung handelt, darf das Produkt nicht in Dehydratationsfällen

verabreicht werden. Außerdem wird von einer subkutanen Verabreichung abgeraten.

6.

NEBENWIRKUNGEN

Glucose 30% ist eine hypertone Lösung. Phlebitis und Gewebereaktionen sind an der Injektionsstelle

theoretisch möglich.

7.

ZIELTIERART(EN)

Rind, Schaf und Ziege.

Bijsluiter – DE versie

Glucose 30 %

8.

DOSIERUNG FÜR JEDE TIERART, ART UND DAUER DER ANWENDUNG

Glukose 30% ist ausschließlich zur intravenösen Verabreichung bestimmt und mittels einer sterilen

Infusion zu verabreichen.

Zur Behandlung einer Acetonämie (Ketose) bei Rindern wird eine Dosierung von 0,5 g Dextrose

je kg Körpergewicht empfohlen; dies entspricht 1,7 ml Glukose 30% je kg Körpergewicht.

Zur Behandlung einer Trächtigkeitstoxämie bei Mutterschafen und Ziegen wird eine Dosierung

von 5-7 g Dextrose empfohlen; dies entspricht 17-23 ml Glukose 30%, 6- bis 8-mal täglich.

9.

HINWEISE FÜR DIE RICHTIGE ANWENDUNG

Die Lösung sollte auf Körpertemperatur verabreicht werden.

10.

WARTEZEIT

Null Tage.

11.

BESONDERE LAGERUNGSHINWEISE

Vor Licht schützen.

Haltbarkeit nach dem Anstechen: 28 Tage bei 25 °C.

Arzneimittel unzugänglich für Kinder aufbewahren.

12.

BESONDERE WARNHINWEISE

Mit Bezug auf den Gebrauch während der Trächtigkeit oder Laktation sind keine Beschränkungen

bekannt.

Dieses Mittel sollte nicht gleichzeitig mit anderen Mitteln verabreicht werden.

Im Falle einer Überdosierung wird (infolge von Glukosurie) ein diuretischer Effekt auftreten.

13.

BESONDERE VORSICHTSMASSNAHMEN FÜR DIE ENTSORGUNG VON NICHT

VERWENDETEM ARZNEIMITTEL ODER VON ABFALLMATERIALIEN, SOFERN

ERFORDERLICH

Damit das Produkt nicht in die Umwelt gelangt, sind die erforderlichen Vorsichtsmaßnahmen zu

treffen.

14.

GENEHMIGUNGSDATUM DER PACKUNGSBEILAGE

Januar 2013

15.

WEITERE ANGABEN

Es werden möglicherweise nicht alle Packungsgrößen in Verkehr gebracht.

Verschreibungspflichtig.

BE-V309145

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Rote - Liste

1-10-2018

Diclofenac-ratiopharm 30 mg/g Gel

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30-9-2018

Roteas (Daiichi Sankyo Europe GmbH)

Roteas (Daiichi Sankyo Europe GmbH)

Roteas (Active substance: edoxaban) - PSUSA - Modification - Commission Decision (2018)5089 of Sun, 30 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/10387/201710

Europe -DG Health and Food Safety

28-9-2018

Diclofenac AbZ 30 mg/g Gel

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19-9-2018

Diclofenac acis 30 mg/g Gel

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17-9-2018

Reminder: the FDA is accepting applications through Sept. 30, 2018, for the #FDAInnovationChallenge for devices to help combat #opioid addiction.   Submissions will be evaluated based on the feasibility, potential public health impact and novelty of the c

Reminder: the FDA is accepting applications through Sept. 30, 2018, for the #FDAInnovationChallenge for devices to help combat #opioid addiction. Submissions will be evaluated based on the feasibility, potential public health impact and novelty of the c

Reminder: the FDA is accepting applications through Sept. 30, 2018, for the #FDAInnovationChallenge for devices to help combat #opioid addiction. Submissions will be evaluated based on the feasibility, potential public health impact and novelty of the concept.

FDA - U.S. Food and Drug Administration

10-9-2018

Gliolan® 30 mg/ml

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4-9-2018

Femikadin® 30

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