Calcamyl-40 MP ad us. vet.

Hauptinformation

  • Handelsname:
  • Calcamyl-40 MP ad us. vet., Infusionslösung
  • 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:
  • Calcamyl-40 MP ad us. vet., Infusionslösung
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Infusionslösung mit Ca, Mg und P für Rinder

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 43498
  • Letzte Änderung:
  • 02-09-2017

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

Calcamyl-40 MP ad us. vet., Infusionslösung

Dr. E. Graeub AG

Infusionslösung mit Ca, Mg und P für Rinder

ATCvet: QA12AX

Zusammensetzung

100 ml Infusionslösung enthalten:

Calcium

(ut C. gluconas et borogluconas)

3.13 g

Magnesium

(ut M. hypophosphis hexahydricus)0.55 g

Phosphorus

(ut M. hypophosphis hexahydricus)1.42 g

Conserv.: E 216: 10 mg, E 218: 90 mg

Aqua ad injectabilia

Fachinformationen Wirkstoffe (CliniPharm)

Calciumgluconat - Magnesiumhypophosphit

Eigenschaften / Wirkungen

Calcamyl-40 MP enthält in ausgewogener Zusammensetzung die Mineralstoffe Calcium,

Magnesium und Phosphor, welche für verschiedene biologische Vorgänge, wie z.B.

Muskelkontraktionen, nervöse Erregungsleitung, Enzymreaktionen etc. lebensnotwendig

sind. Calcium besitzt einen stabilisierenden Effekt auf Membranen; es wirkt einer erhöhten

Gefässpermeabilität entgegen. Zudem hat Calcium antiphlogistische und antiallergische

Eigenschaften. Calciummangel führt bei der Milchkuh zu Krankheiten wie:

lebensbedrohliche hypocalcämische Gebärparese (Festliegen), fortschreitende

Muskellähmung, Kreislaufschwäche. Hypomagnesämische Zustände können ebenfalls

Festliegen verursachen. Ein Abfall des Phosphatspiegels im Blut kann zu einem

verminderten Ansprechen auf eine Calciumtherapie führen.

Indikationen

Rind: Gebärparese, Festliegen, Stall- und Weidetetanie.

Rind, langsam intravenös:

50 ml pro 100 kg KGW

Rind, subkutan auf mehrere Stellen verteilt:

100 - 200 ml

Anwendungseinschränkungen

Kontraindikationen

Schwere Niereninsuffizienz, Hypercalcämie.

Vorsichtsmassnahmen

Wie bei allen Calcium-Infusionen ist eine Herzkontrolle empfohlen.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Zu schnelle Infusion kann zu allergischen Erscheinungen führen. Eventuell auftretende

Gewebeschwellungen klingen nach einigen Tagen wieder ab.

keine

Wechselwirkungen

Calcium-Ionen und Herzglycoside wirken synergistisch. Dieser Effekt kann zu einem

Herzstillstand führen.

Sonstige Hinweise

Das Präparat darf nur bis zu dem auf der Packung mit "Exp" bezeichneten Datum

verwendet werden.

-Aufbrauchfrist nach erster Entnahme: 4 Wochen.

-Medikament ausser Reichweite von Kindern aufbewahren.

-Bei Raumtemperatur (15 - 25°C) aufbewahren.

Packungen

Infusionsflasche zu 500 ml

Abgabekategorie: B

Swissmedic Nr. 43'498

Informationsstand: 06/2005

Dieser Text ist behördlich genehmigt.

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Versican Plus DHPPi/L4R ad us. vet.

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Versican Plus L4 ad us. vet.

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Institut für Veterinärpharmakologie und toxikologie

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Versican Plus Pi/L4 ad us. vet.

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Perlutex ad us. vet., Tabletten

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Activyl TickPlus spot-on Hund M ad us. vet., insektizide Loesung zum Auftragen auf die Haut

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Institut für Veterinärpharmakologie und toxikologie

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Institut für Veterinärpharmakologie und toxikologie

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Institut für Veterinärpharmakologie und toxikologie

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Institut für Veterinärpharmakologie und toxikologie

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Institut für Veterinärpharmakologie und toxikologie

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21-12-2018

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19-12-2018

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FDA - U.S. Food and Drug Administration

19-12-2018

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FDA - U.S. Food and Drug Administration

18-12-2018

#DYK December is #SafeToysAndGiftsMonth. Check out @US_FDA's Consumer Update on how to keep kids safe with toys containing lasers:  https://go.usa.gov/xEx2r  #FDApic.twitter.com/57pZAmSb9r

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FDA - U.S. Food and Drug Administration

14-12-2018

GE Healthcare Recalls CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit. @US_FDA @US has identified this as a Class I Recall, the most serious type recall. Read more about the recall here:  https://go.usa.gov/xE38

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FDA - U.S. Food and Drug Administration

14-12-2018

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FDA - U.S. Food and Drug Administration

14-12-2018

Relvar Ellipta (GlaxoSmithKline (Ireland) Limited)

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Europe -DG Health and Food Safety

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.@US_FDA is emphasizing the importance of manual cleaning prior to disinfection or sterilization and proper servicing of duodenoscopes. Read more:  https://go.usa.gov/xPShF  #MedicalDevice #FDApic.twitter.com/HiJbgPnsPt

.@US_FDA is emphasizing the importance of manual cleaning prior to disinfection or sterilization and proper servicing of duodenoscopes. Read more: https://go.usa.gov/xPShF  #MedicalDevice #FDApic.twitter.com/HiJbgPnsPt

. @US_FDA is emphasizing the importance of manual cleaning prior to disinfection or sterilization and proper servicing of duodenoscopes. Read more: https://go.usa.gov/xPShF  #MedicalDevice #FDA pic.twitter.com/HiJbgPnsPt

FDA - U.S. Food and Drug Administration

7-12-2018

Ferrlecit® 40 mg/Ferrlecit 62,5 mg

Rote - Liste

1-12-2018

.@US_FDA scientists have replicated an imaging clinical trial using computer methods, suggesting in silico trials hold promise for regulatory evaluation.  https://ja.ma/2rdAtre pic.twitter.com/XiTbPfEkcj

.@US_FDA scientists have replicated an imaging clinical trial using computer methods, suggesting in silico trials hold promise for regulatory evaluation. https://ja.ma/2rdAtre pic.twitter.com/XiTbPfEkcj

. @US_FDA scientists have replicated an imaging clinical trial using computer methods, suggesting in silico trials hold promise for regulatory evaluation. https://ja.ma/2rdAtre  pic.twitter.com/XiTbPfEkcj

FDA - U.S. Food and Drug Administration

30-11-2018

#FDA In Brief: @US_FDA takes steps to advance the safety and accuracy of  blood glucose monitors to empower patients with diabetes with reliable  tools to manage their health. Read more:  https://go.usa.gov/xPMyA   #MedicalDevice

#FDA In Brief: @US_FDA takes steps to advance the safety and accuracy of blood glucose monitors to empower patients with diabetes with reliable tools to manage their health. Read more: https://go.usa.gov/xPMyA  #MedicalDevice

#FDA In Brief: @US_FDA takes steps to advance the safety and accuracy of blood glucose monitors to empower patients with diabetes with reliable tools to manage their health. Read more: https://go.usa.gov/xPMyA  #MedicalDevice

FDA - U.S. Food and Drug Administration

30-11-2018

.@US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall:  https://go.usa.gov/xPMEn  #MedicalDevicepic.twitter.com/YU9Iq

.@US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn  #MedicalDevicepic.twitter.com/YU9Iq

. @US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn  #MedicalDevice pic.twitter.com/YU9Iq3Yw0b

FDA - U.S. Food and Drug Administration

30-11-2018

.@US_FDA issues class I recall, the most serious type pf recall: Zimmer  Biomet, Inc. Recalls Spinal Fusion & Long Bone Stimulators Due to Lack  of Adequate Validation and Controls to Ensure Product Cleanliness. Read  more about the recall:  https://go.us

.@US_FDA issues class I recall, the most serious type pf recall: Zimmer Biomet, Inc. Recalls Spinal Fusion & Long Bone Stimulators Due to Lack of Adequate Validation and Controls to Ensure Product Cleanliness. Read more about the recall: https://go.us

. @US_FDA issues class I recall, the most serious type pf recall: Zimmer Biomet, Inc. Recalls Spinal Fusion & Long Bone Stimulators Due to Lack of Adequate Validation and Controls to Ensure Product Cleanliness. Read more about the recall: https://go.usa.gov/xPMEK  #MedicalDevice pic.twitter.com/M55ddC98wW

FDA - U.S. Food and Drug Administration

30-11-2018

.@US_FDA has selected 8 novel medical devices as participants in #FDA’s Innovation Challenge to address the #OpioidEpidemic by preventing and treating opioid use disorder. #FDAInnovationChallenge

.@US_FDA has selected 8 novel medical devices as participants in #FDA’s Innovation Challenge to address the #OpioidEpidemic by preventing and treating opioid use disorder. #FDAInnovationChallenge

. @US_FDA has selected 8 novel medical devices as participants in #FDA’s Innovation Challenge to address the #OpioidEpidemic by preventing and treating opioid use disorder. #FDAInnovationChallenge

FDA - U.S. Food and Drug Administration

29-11-2018

Andriol Testocaps 40 mg Kapseln

Rote - Liste

27-11-2018

Paroxetin-ratiopharm 40 mg Tabletten

Rote - Liste

26-11-2018

#DYK November is #NationalHealthySkinMonth. Are you thinking about getting Dermal Fillers? Check out the @US_FDA's information on Dermal Fillers before you do:  https://go.usa.gov/xPHtk   #FDA #MedicalDevice

#DYK November is #NationalHealthySkinMonth. Are you thinking about getting Dermal Fillers? Check out the @US_FDA's information on Dermal Fillers before you do: https://go.usa.gov/xPHtk  #FDA #MedicalDevice

#DYK November is #NationalHealthySkinMonth. Are you thinking about getting Dermal Fillers? Check out the @US_FDA's information on Dermal Fillers before you do: https://go.usa.gov/xPHtk  #FDA #MedicalDevice

FDA - U.S. Food and Drug Administration