Hyalovet 20 ad us. vet.

Hauptinformation

  • Handelsname:
  • Hyalovet® 20 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:
  • Hyalovet® 20 ad us. vet., Injektionslösung
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Hyaluronsäurelösung für das Pferd: Injektionslösung für intraartikuläre Verabreichung

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 45449
  • Letzte Änderung:
  • 02-09-2017

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

Hyalovet

20 ad us. vet., Injektionslösung

TRB Chemedica International SA

Hyaluronsäurelösung für das Pferd: Injektionslösung für intraartikuläre

Verabreichung

ATCvet: QM09AX01

Zusammensetzung

Hochviskose wässrige Lösung einer definierten Molekularfraktion von gereinigter

Hyaluronsäure. Eine Spritzampulle oder ein Injektionsfläschchen enthalten jeweils:

Wirkstoff: Natrii hyaluronas 20 mg, Hilfsstoffe: Natrii chloridum, Natrii

dihydrogenophosphas, Dinatrii phosphas dodecahydricus, Aqua q.s. ad sol. pro 2 ml

Fachinformationen Wirkstoffe (CliniPharm)

Hyaluronsäure

Eigenschaften / Wirkungen

Die Hyaluronsäure ist der Prototyp einer grossen Familie von Saccharidbiopolymeren

(Glykosaminoglykane oder Mukopolysaccharide), die wichtige Bestandteile aller

extrazellulären Gewebestrukturen sind, Knorpel und Synovialflüssigkeit eingeschlossen.

Die Hyalovet

Wirksubstanz ist eine spezifische hochgereinigte Hyaluronsäurefraktion mit

definierter Molekularkettenlänge (2500 - 3500 Saccharideinheiten), die besondere

biochemische, physikalische und pharmakologische Eigenschaften besitzt.

Die intraartikuläre Injektion dieser biologischen Substanz ins erkrankte Pferdegelenk führt

eine Verbesserung der Gelenkfunktion herbei, bedingt durch die Normalisierung der

viskoelastischen Eigenschaften der Synovialflüssigkeit und die Aktivierung der

Gewebeheilungsprozesse im Gelenkknorpel.

Indikationen

Gelenkerkrankungen vom Pferd, verursacht durch:

Osteoarthrose mit oder ohne

Entzündungserscheinungen,

-akute oder chronische Synovitis,

-degenerative Prozesse im Gelenkknorpel,

-Osteochondrosis dissecans.

Adjuvans bei der Behandlung von Splitter- oder Sesamoidbrüchen.

Dosierung / Anwendung

2 ml pro Gelenk (eine Spritzampulle oder ein Injektionsfläschchen). Mehrere Gelenke

können gleichzeitig behandelt werden. Im Bedarfsfall kann die Injektion nach einer oder

mehreren Wochen wiederholt werden.

Anwendungseinschränkungen

Kontraindikationen

Kontraindikationen sind nicht bekannt.

Vorsichtsmassnahmen

Die Injektion ist unter streng aseptischen Bedingungen auszuführen.

Gewebeschädigungen sind zu vermeiden.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Vorübergehende Lokalreaktionen können vereinzelt auftreten.

Keine.

Wechselwirkungen

Nicht bekannt.

Sonstige Hinweise

Das Medikament kann bloss bis zu dem mit "expir." bezeichneten Datum verwendet

werden. Bei Raumtemperatur (15 - 25°C) und vor Feuchtigkeit geschützt aufbewahren.

Reste der Lösung nicht mehr verwenden. Das Präparat ist von Kindern fernzuhalten.

Packungen

2 ml Spritzampulle mit 19-G-Nadel

2 ml Injektionsfläschchen

Abgabekategorie: A

Hersteller

Fidia Farmaceutici S.p.A. - Abano Terme (PD) Italien

Swissmedic Nr. 45'449

Informationsstand: 06/2002

Dieser Text ist behördlich genehmigt.

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