Ig-PRO D Oral Care

Hauptinformation

  • Handelsname:
  • Ig-PRO® D Oral Care
  • Verwenden für:
  • Tiere
  • Art der Medizin:
  • Nahrungsergänzungsmittel

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:
  • Ig-PRO® D Oral Care
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiebereich:
  • Ergänzungsfuttermittel für Hunde zur Zusatzversorgung mit wichtigen Nährstoffen und zur Unterstützung der Maulhygiene.

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • α CH 32707
  • Letzte Änderung:
  • 22-01-2018

Packungsbeilage

ufamed AG

Ergänzungsfuttermittel für Hunde zur Zusatzversorgung mit wichtigen Nährstoffen und zur

Unterstützung der Maulhygiene.

Inhalt

Zusammensetzung:

Pflanzliche Öle und Fette (Sonnenblume), Eiprodukte (getrocknet) 17%, Hefeprodukt,

Dicalciumphosphat, Erzeugnisse aus der Verarbeitung von Kräutern (Petersilie) 5%

Analytische Bestandteile:

Rohprotein 11,50%, Rohöle und -fette 62,50%, Rohfaser 0,50%, Rohasche 10,50%, Salzsäure unlösliche

Asche 3,50%, Calcium 1,60%, Natrium 0,01%, Kalium 0,25%

Zusatzstoffe pro kg:

Ernährungsphysiologische Zusatzstoffe

Vitamin D

(E671) 50`000 I.E., Vitamin E (all rac-alpha-Tocopherylacetat (3a700)) 5`000 mg, Zink

(Zinkacetat Dihydrat (3b601)) 2`000 mg

Eigenschaften

Verhindert aufgrund spezifischer Ig- Pro

D Oral Care Ei-Pulvermischung die Besiedelung der

Maulhöhle mit Bakterien.

Die Bakterien werden durch spezifische Ig Y Antikörper neutralisiert.

Der Zusatz von Petersilie sorgt für einen frischen Atem.

Vitamin D ist zusammen mit Calcium und Phosphor am Mineralisierungsprozess der Zähne beteiligt.

Vitamin E ist als Oxidationsschutz für die ungesättigten Fettsäuren beigesetzt und Zink als Bestandteil

zahlreicher Enzyme.

Anwendungsmöglichkeiten

Schlechter

Atemgeruch/Mundgeruch

-Zahnbeläge/Plaques

-Prophylaxe von Zahnsteinbildung

Anwendung / Gebrauch

Fütterungsempfehlung:

Idealerweise sollten die Zähne des Hundes zuerst von einem Tierarzt überprüft und ggf. professionell

gereinigt und behandelt werden.

Einmal täglich Ig-Pro

D Oral Care über das Futter verabreichen oder ähnlich einer Zahnpasta auf den

Zähnen und dem Zahnfleisch verteilen (Bürsten ist nicht erforderlich).

Hunde < 15 kg:

2 - 3 cm

Paste

Hunde von 15 - 30 kg:

3 - 4 cm

Paste

Hunde > 30 kg:

4 - 5 cm

Paste

Empfohlene Fütterungsdauer:

Dauerhaft täglich oder als Kur über mindestens 3 Wochen regelmässig wiederholen.

Fütterungshinweis:

Aufgrund des höheren Gehaltes an Zink im Vergleich zu Alleinfuttermitteln darf dieses

Ergänzungsfuttermittel nur an Hunde mit bis zu 4% der Tagesration verfüttert werden.

Sonstige Hinweise

Kühl (5 - 25°C), frostfrei, trocken und vor lichtgeschützt lagern! Nach Anbruch schnellstmöglich

aufbrauchen.

Handelsformen

140 ml Tube

Agroscope−Zulassungsnummer: α CH 32707

Informationsstand: 01.12.2017

17-7-2018

Dringende Sicherheitsinformation zu Sectio Set Bielefeld incl. Safil and Novosyn von Mölnlycke Health Care AB

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Weitere Informationen sowie Details zum Produkt entnehmen Sie bitte der anliegenden Kundeninformation des Herstellers.

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Saje Natural Wellness is warning customers not to use Splish Splash Gentle Baby Wash, 8.5 fl. oz. and 1.7 fl. oz. (found in the Wee and Well Gentle Baby Care Kit) as it may contain the bacteria Pseudomonas aeruginosa. Pseudomonas aeruginosa is an opportunistic pathogen that causes infection and results in bacteria in the blood, particularly in individuals with compromised immune systems.

FDA - U.S. Food and Drug Administration

29-6-2018

Medicines Safety Update, Volume 9, Number 2, June 2018

Medicines Safety Update, Volume 9, Number 2, June 2018

Oral methotrexate dosing, medicines associated with a risk of neuropsychiatric adverse events, and clozapine and gastrointestinal effects

Therapeutic Goods Administration - Australia

25-6-2018

FDA approves first drug comprised of an active ingredient derived from marijuana to treat rare, severe forms of epilepsy

FDA approves first drug comprised of an active ingredient derived from marijuana to treat rare, severe forms of epilepsy

FDA approved Epidiolex (cannabidiol) oral solution, the first drug comprised of an active ingredient derived from marijuana, to treat two rare and severe forms of epilepsy.

FDA - U.S. Food and Drug Administration

19-6-2018

Various Aortic Endovascular Graft Systems: Letter to Health Care Providers - UPDATE on Type III Endoleaks

Various Aortic Endovascular Graft Systems: Letter to Health Care Providers - UPDATE on Type III Endoleaks

Based on new information, the Endologix AFX with Strata device is at greater risk for a Type III endoleak compared to other endovascular AAA graft systems.

FDA - U.S. Food and Drug Administration

13-6-2018

Dringende Sicherheitsinformation zu Procedure trays: Bandscheiben Tray KH Vilsbiburg Spinale, LWS-Set Worms von Mölnlycke Health Care AB

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Weitere Informationen sowie Details zum Produkt entnehmen Sie bitte der anliegenden Kundeninformation des Herstellers.

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

12-6-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on new efforts to advance medical product communications to support drug competition and value-based health care

Statement from FDA Commissioner Scott Gottlieb, M.D., on new efforts to advance medical product communications to support drug competition and value-based health care

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FDA - U.S. Food and Drug Administration

4-6-2018

Liquid-filled Intragastric Balloons by Apollo Endosurgery and ReShape Lifesciences: Letter to Health Care Providers - New Labeling About Potential Risks

Liquid-filled Intragastric Balloons by Apollo Endosurgery and ReShape Lifesciences: Letter to Health Care Providers - New Labeling About Potential Risks

FDA has approved new labeling for the Orbera and ReShape balloon systems with more information about possible death associated with the use of these devices.

FDA - U.S. Food and Drug Administration

31-5-2018

Vitakraft Vita Care Antiparasit-Halsband ad us. vet., fuer Katzen

Vitakraft Vita Care Antiparasit-Halsband ad us. vet., fuer Katzen

● Die Zulassung ist am 31.05.2018 erloschen.

Institut für Veterinärpharmakologie und toxikologie

29-5-2018

TAYTULLA (norethindrone acetate and ethinyl estradiol capsules and ferrous fumarate capsules) by Allergan: Recall - Due to Out of Sequence Capsules

TAYTULLA (norethindrone acetate and ethinyl estradiol capsules and ferrous fumarate capsules) by Allergan: Recall - Due to Out of Sequence Capsules

Allergan recently identified, through a physician report, that four placebo capsules were placed out of order in a sample pack of TAYTULLA. Specifically, the first four days of therapy had four non-hormonal placebo capsules instead of active capsules. As a result of this packaging error, oral contraceptive capsules, that are taken out of sequence, may place the user at risk for contraceptive failure and unintended pregnancy. The reversing of the order may not be apparent to either new users or previous ...

FDA - U.S. Food and Drug Administration

29-5-2018

Dringende Sicherheitsinformation zu XO 4 Unit von XO Care A/S

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Weitere Informationen sowie Details zum Produkt entnehmen Sie bitte der anliegenden Kundeninformation des Herstellers.

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

29-5-2018

Herausforderungen und offene „To-dos“ für die pharmazeutische Industrie

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Vortragsfolien von Verband Forschender Arzneimittelhersteller e. V., Bundesverband der Arzneimittel-Hersteller e. V., Bundesverband der Pharmazeutischen Industrie e. V., Pro Generika e. V., im Rahmen der Veranstaltung "BfArM im Dialog - Arzneimittelfälschungen und Umsetzung der Fälschungsschutzrichtlinie" vom 8. Mai 2018

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

24-5-2018

FDA Approves Semintra, the First FDA-approved Animal Drug for the Control of Systemic Hypertension in Cats

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The FDA has approved Semintra (telmisartan oral solution), the first FDA-approved animal drug to control systemic hypertension in cats. Semintra is an oral solution administered either directly into the cat’s mouth or on top of a small amount of food.

FDA - U.S. Food and Drug Administration

23-5-2018

Merrick Pet Care Voluntarily Recalls Limited Amount of Good Buddy and Backcountry Treats Containing Beef Due to Potentially Elevated Levels of Thyroid Hormone

Merrick Pet Care Voluntarily Recalls Limited Amount of Good Buddy and Backcountry Treats Containing Beef Due to Potentially Elevated Levels of Thyroid Hormone

Merrick Pet Care, of Amarillo, Texas, is initiating a voluntary recall of a limited amount of beef dog treat varieties due to the potential that they contain elevated levels of a naturally-occurring beef thyroid hormone.

FDA - U.S. Food and Drug Administration

23-5-2018

FDA takes action against the use of OTC benzocaine teething products due to serious safety risk, lack of benefit

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OTC oral health products containing benzocaine for the temporary relief of sore gums due to teething in infants or children should no longer be marketed. FDA is asking companies to stop selling these products for such use and requesting that companies add new warnings to all other benzocaine oral health products to describe certain serious risks.

FDA - U.S. Food and Drug Administration

23-5-2018

Oral Over-the-Counter Benzocaine Products: Drug Safety Communication  - Risk of Serious and Potentially Fatal Blood Disorder

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Oral over-the-counter benzocaine products should not be used to treat infants and children younger than 2 years and should only be used in adults and children 2 years and older if they contain certain warnings on the drug label.

FDA - U.S. Food and Drug Administration

22-5-2018

Risk of serious and potentially fatal blood disorder prompts FDA action on oral over-the-counter benzocaine products used for teething and mouth pain and prescription local anesthetics

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FDA is taking safety actions regarding over-the-counter benzocaine oral drug products and prescription local anesthetics.

FDA - U.S. Food and Drug Administration

18-5-2018

Keytruda (pembrolizumab) or Tecentriq (atezolizumab): FDA Alerts Health Care Professionals and Investigators: FDA Statement - Decreased Survival in Some Patients in Clinical Trials Associated with Monotherapy

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Early reviews found patients in the monotherapy arms of both trials with PD-L1 low status had decreased survival compared to patients who received cisplatin- or carboplatin-based chemotherapy.

FDA - U.S. Food and Drug Administration

8-5-2018

Neurovascular Stents Used for Stent-Assisted Coiling (SAC): Letter to Health Care Providers - Recommendations Associated With the Use of These Devices in the Treatment of Unruptured Brain Aneurysms

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The FDA has received reports associated with the use of these devices in the treatment of unruptured brain aneurysms that suggest some events of peri-procedural stroke and/or death may have been related to procedural risks or patient selection related factors. These factors include patients who had serious co-morbidities resulting in a reduced life expectancy, or who were intolerant to required anticoagulation or anti-platelet therapy.

FDA - U.S. Food and Drug Administration

2-5-2018

April 17, 2018: Tampa Resident Sentenced to More Than 20 Years in Federal Prison for Tricare Health Care Fraud Scheme

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FDA - U.S. Food and Drug Administration

25-4-2018

Magnetic Resonance-guided Laser Interstitial Thermal Therapy (MRgLITT) Devices: Letter to Health Care Providers - Risk of Tissue Overheating Due to Inaccurate Magnetic Resonance Thermometry

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FDA is currently evaluating data which suggests that potentially inaccurate MR thermometry information can be displayed during treatment. Posted 04/25/2018

FDA - U.S. Food and Drug Administration

17-4-2018

March 27, 2018: Compounding Pharmacy Owner Sentenced to Five Years in Prison for $10.5 Million Health Care Fraud

March 27, 2018: Compounding Pharmacy Owner Sentenced to Five Years in Prison for $10.5 Million Health Care Fraud

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FDA - U.S. Food and Drug Administration

20-3-2018

Medicines Safety Update, Volume 9, Number 1, February-March 2018

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First-generation oral sedating antihistamines – use in children, Suvorexant (Belsomra) – next day effects, Desvenlafaxine (Pristiq) recommended dose, Miconazole and potential interaction with warfarin

Therapeutic Goods Administration - Australia

14-3-2018

Is It a Cold or the Flu? Prevention, Symptoms, Treatments

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21-8-2017

Access to a European primary and/or secondary care medical database - EMA/2016/33/PH

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Contract award notice

Europe - EFSA - European Food Safety Authority EFSA Journal

24-6-2014

Focus on correct dose of Pro-Epanutin

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The Danish Health and Medicines Authority encourages hospitals to pay special attention to the risk of dose errors of the anticonvulsant medicine Pro-Epanutin.

Danish Medicines Agency

28-5-2014

More than 10,000 websites shut down in global operation

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1-4-2014

Danish Pharmacovigilance Update 27 February 2014

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Danish Medicines Agency

17-2-2014

Danish Pharmacovigilance Update 19 December 2013

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In this issue of Danish Pharmacovigilance Update: Patients with mechanical heart valves should not be treated with the new oral anticoagulants Pradaxa®, Xarelto® and Eliquis®.

Danish Medicines Agency

13-6-2018

Colibiogen® oral

Rote - Liste

5-6-2018

Lasix® oral

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4-6-2018

UPDATE to Letter to Health Care Providers: Potential risks with liquid-filled intragastric balloons – Additional Information Regarding Death Reports-  https://go.usa.gov/xQGf8  #FDA #MedicalDevice

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FDA - U.S. Food and Drug Administration

29-5-2018

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Europe -DG Health and Food Safety

15-5-2018

Take care of your heart. Share these 4 tips for better heart health:  http://go.usa.gov/xXG7h  #NWHWpic.twitter.com/h1j6iHmvny

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Take care of your heart. Share these 4 tips for better heart health: http://go.usa.gov/xXG7h  #NWHW pic.twitter.com/h1j6iHmvny

FDA - U.S. Food and Drug Administration

14-5-2018

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Pro tip: Use our checklist as a starting point.  https://go.usa.gov/xQg4q  #NWHWpic.twitter.com/A44He0N4sf

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5-12-2017

Rabitec (IDT Biologika GmbH)

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Europe -DG Health and Food Safety