Koi Med Tincture ad us. vet.[M]

Hauptinformation

  • Handelsname:
  • Koi Med Tincture ad us. vet.[M], Flüssigkeit
  • Darreichungsform:
  • Flüssigkeit
  • 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:
  • Koi Med Tincture ad us. vet.[M], Flüssigkeit
    Schweiz
  • Sprache:
  • Deutsch

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 59041
  • Letzte Änderung:
  • 02-09-2017

Packungsbeilage

Koi Med Tincture ad us. vet.

, Flüssigkeit

Zulassung im

Meldeverfahren

Swissmedic

fishmed GmbH

ATCvet: QD03

Zusammensetzung

Tinctura 500 mg ex rhei radix, Acidum salicylicum 100 mg, excipiens ad solutionem pro

10 ml.

Fachinformationen Wirkstoffe (CliniPharm)

Medizinal-Rhabarber - Salicylsäure

Zielspezies

Für Zierfische

Anwendungsgebiet

Behandlung und Desinfektion von Hautwunden bei Zierfischen.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Sonstige Hinweise

Für weitere Informationen wenden Sie sich an die Zulassungsinhaberin (Fishmed GmbH).

Packungen

10 ml

Abgabekategorie: D

Swissmedic Nr. 59'041

Informationsstand: 09/2007

Dieser Text ist behördlich genehmigt.

19-10-2018

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Cedar’s Mediterranean Foods, of Ward Hill, MA is voluntarily recalling Cedar’s Chickpea Salad 8 oz. because it may contain undeclared edamame (soy). People who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

19-10-2018

Reclamecode voor medische cosmetische behandelingen

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16-10-2018

FDA and DHS increase coordination of responses to medical device cybersecurity threats under new partnership; a part of the two agencies’ broader effort to protect patient safety

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10-10-2018

Sprayology Issues Voluntary Nationwide Recall of Homeopathic Aqueous-Based Medicines Due to Microbial Contamination

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FDA - U.S. Food and Drug Administration

10-10-2018

Minister Bruins tekent Green Deal voor duurzame zorg

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Credelio 56 mg ad us. vet., Kautabletten fuer Hunde

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● Die Neuzulassung erfolgte am 10.10.2018.

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Credelio 112 mg ad us. vet., Kautabletten fuer Hunde

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● Die Neuzulassung erfolgte am 10.10.2018.

Institut für Veterinärpharmakologie und toxikologie

10-10-2018

Credelio 225 mg ad us. vet., Kautabletten fuer Hunde

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● Die Neuzulassung erfolgte am 10.10.2018.

Institut für Veterinärpharmakologie und toxikologie

10-10-2018

Credelio 450 mg ad us. vet., Kautabletten fuer Hunde

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● Die Neuzulassung erfolgte am 10.10.2018.

Institut für Veterinärpharmakologie und toxikologie

10-10-2018

Credelio 900 mg ad us. vet., Kautabletten fuer Hunde

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● Die Neuzulassung erfolgte am 10.10.2018.

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9-10-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on new efforts to advance the development of generic copies of complex drugs to improve patient access to medicines

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9-10-2018

Essity Professional Hygiene North America LLC recalls Tork Foam Soap Extra Mild SKU

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The recalled product is potentially contaminated with the bacteria Burkholderia cepacia. B. cepacia is found in soil and water and poses little medical risk to healthy people.

Health Canada

9-10-2018

Metacam 5 mg/ml ad us. vet., Injektionsloesung

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● Verzicht Packungsgrösse 10 ml

Institut für Veterinärpharmakologie und toxikologie

4-10-2018

Nederland organiseert wereldwijde conferentie tegen antibioticaresistentie

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3-10-2018

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Sinds enkele jaren onderhandelt de minister voor Medische Zorg met fabrikanten van nieuwe en zeer dure geneesmiddelen. Doel is om deze waardevolle innovatieve geneesmiddelen tegen aanvaardbare kosten toegankelijk te maken en te houden voor de patiënt. Dit heeft in 2017 geleid tot een kostenverlaging van in totaal 132 miljoen euro. Dat heeft minister Bruno Bruins aan de Tweede Kamer laten weten. Op basis van de prijs die fabrikanten eerst vroegen zou er sprake zijn van 457 miljoen aan uitgaven aan de betr...

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Metacam 2 mg/ml Katzen ad us. vet., Injektionsloesung

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Institut für Veterinärpharmakologie und toxikologie

2-10-2018

Forthyron 200 ad us. vet., Tabletten

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● Die Zulassung ist am 02.10.2018 erloschen.

Institut für Veterinärpharmakologie und toxikologie

2-10-2018

Forthyron 400 ad us. vet., Tabletten

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● Die Zulassung ist am 02.10.2018 erloschen.

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1-10-2018

Statement from FDA Commissioner Scott Gottlieb, M.D. on FDA’s efforts to strengthen the agency’s medical device cybersecurity program as part of its mission to protect patients

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1-10-2018

Minister Bruno Bruins naar ministeriële G20-bijeenkomst over gezondheid

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FDA awards 12 grants to fund new clinical trials to advance the development of medical products for the treatment of rare diseases

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19-10-2018

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18-10-2018

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17-10-2018

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15-10-2018

We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4.

 http://fema.gov/hurricane-michael-rumor-co

We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4. http://fema.gov/hurricane-michael-rumor-co

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10-10-2018

Diversity in research means more treatments work for more people. Join #ResearchDiversity Day on October 23rd for a day-long discussion of diversity in study recruitment and research. Join us! @Alzheimers_NIHpic.twitter.com/AwYhetCBiw

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2-10-2018

Zavesca (Janssen-Cilag International NV)

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Dynastat (Pfizer Europe MA EEIG)

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2-10-2018

Retacrit (Pfizer Europe MA EEIG)

Retacrit (Pfizer Europe MA EEIG)

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2-10-2018

HALAVEN (Eisai GmbH)

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Imraldi (Samsung Bioepis UK Limited)

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2-10-2018

Nexium Control (Pfizer Healthcare Ireland)

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1-10-2018

My statement on the #FDA’s new efforts to strengthen the agency’s medical device cybersecurity program as part of our mission to protect patients  http://go.usa.gov/xPBK2 pic.twitter.com/8w5m5itceW

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1-10-2018

MS-H vaccine (Pharmsure Veterinary Products Europe Ltd)

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1-10-2018

Verzenios (Eli Lilly Nederland B.V.)

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1-10-2018

EU/3/16/1762 (Pharma Gateway AB)

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Europe -DG Health and Food Safety

1-10-2018

EU/3/05/328 (Celgene Europe B.V.)

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1-10-2018

EU/3/05/279 (Celgene Europe B.V.)

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Europe -DG Health and Food Safety

1-10-2018

EU/3/03/133 (Shire Orphan Therapies GmbH)

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EU/3/03/133 (Active substance: Icatibant acetate) - Transfer of orphan designation - Commission Decision (2018)6432 of Mon, 01 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/054/02/T/01

Europe -DG Health and Food Safety

1-10-2018

Gefitinib Mylan (Mylan S.A.S.)

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Europe -DG Health and Food Safety

30-9-2018

Roteas (Daiichi Sankyo Europe GmbH)

Roteas (Daiichi Sankyo Europe GmbH)

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26-9-2018

FORTEKOR PLUS (Elanco GmbH)

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Europe -DG Health and Food Safety

26-9-2018

Comfortis (Elanco GmbH)

Comfortis (Elanco GmbH)

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Europe -DG Health and Food Safety

26-9-2018

Kexxtone (Elanco GmbH)

Kexxtone (Elanco GmbH)

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25-9-2018

Udenyca (ERA Consulting GmbH)

Udenyca (ERA Consulting GmbH)

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Europe -DG Health and Food Safety

25-9-2018

Inovelon (Eisai GmbH)

Inovelon (Eisai GmbH)

Inovelon (Active substance: Rufinamide) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6283 of Tue, 25 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/660/T/48

Europe -DG Health and Food Safety

25-9-2018

Zonegran (Eisai GmbH)

Zonegran (Eisai GmbH)

Zonegran (Active substance: zonisamide) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6285 of Tue, 25 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/577/T/90

Europe -DG Health and Food Safety

25-9-2018

Slenyto (RAD Neurim Pharmaceuticals EEC Limited)

Slenyto (RAD Neurim Pharmaceuticals EEC Limited)

Slenyto (Active substance: melatonin) - Centralised - Authorisation - Commission Decision (2018)6223 of Tue, 25 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4425

Europe -DG Health and Food Safety

25-9-2018

Brilique (AstraZeneca AB)

Brilique (AstraZeneca AB)

Brilique (Active substance: ticagrelor) - PSUSA - Modification - Commission Decision (2018)6282 of Tue, 25 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1241/PSUSA/2948/201712

Europe -DG Health and Food Safety

25-9-2018

Fycompa (Eisai GmbH)

Fycompa (Eisai GmbH)

Fycompa (Active substance: Perampanel) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6280 of Tue, 25 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/002434/T/0040

Europe -DG Health and Food Safety

25-9-2018

Opsumit (Janssen-Cilag International NV)

Opsumit (Janssen-Cilag International NV)

Opsumit (Active substance: macitentan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6279 of Tue, 25 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/002697/T/0028

Europe -DG Health and Food Safety

25-9-2018

Imfinzi (AstraZeneca AB)

Imfinzi (AstraZeneca AB)

Imfinzi (Active substance: durvalumab) - Centralised - Authorisation - Commission Decision (2018)6289 of Tue, 25 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/004771/0000

Europe -DG Health and Food Safety

25-9-2018

Pelgraz (Accord Healthcare Limited)

Pelgraz (Accord Healthcare Limited)

Pelgraz (Active substance: pegfilgrastim) - Centralised - Authorisation - Commission Decision (2018)6288 of Tue, 25 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/003961/0000

Europe -DG Health and Food Safety

24-9-2018

News and press releases:  Companies stepping up efforts to ensure medicine supply post Brexit

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Focus is now on 39 centrally authorised medicines, down from 108

Europe - EMA - European Medicines Agency

24-9-2018

NeuroBloc (Sloan Pharma S.a.r.l.)

NeuroBloc (Sloan Pharma S.a.r.l.)

NeuroBloc (Active substance: Botulinum Toxin Type B) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6221 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/000301/T/0101

Europe -DG Health and Food Safety

24-9-2018

Renvela (Genzyme Europe B.V.)

Renvela (Genzyme Europe B.V.)

Renvela (Active substance: sevelamer (carbonate)) - Centralised - Variation - Commission Decision (2018)6225 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/993/X/39

Europe -DG Health and Food Safety

24-9-2018

Deferiprone Lipomed (Lipomed GmbH)

Deferiprone Lipomed (Lipomed GmbH)

Deferiprone Lipomed (Active substance: Deferiprone) - Centralised - Authorisation - Commission Decision (2018)6233 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4710

Europe -DG Health and Food Safety

24-9-2018

Inhixa (Techdow Europe AB)

Inhixa (Techdow Europe AB)

Inhixa (Active substance: enoxaparin sodium) - Centralised - Variation - Commission Decision (2018)6101 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4264/X/18, 26

Europe -DG Health and Food Safety