RIBES PET SYMBIO GATTO

Informazioni principali

  • Nome commerciale:
  • RIBES PET SYMBIO GATTO
  • Forma farmaceutica:
  • Orale
  • Confezione:
  • 30 perle, in blister
  • Tipo di ricetta:
  • Libera vendita
  • Utilizzare per:
  • Animali
  • Tipo di medicina:
  • Nutrizionale

Documenti

  • per i professionisti:
  • Il foglio illustrativo per questo prodotto non è al momento disponibile, é possibile inviare una richiesta al nostro Servizio Clienti ed essere avvisati nel momento in cui è disponibile sulla nostra piattaforma.


    Richiedi il foglio illustrativo per i professionisti.

Localizzazione

  • Disponibile in:
  • RIBES PET SYMBIO GATTO
    Italia
  • Lingua:
  • italiano

Informazioni terapeutiche

  • Gruppo terapeutico:
  • Gatti
  • Area terapeutica:
  • Tutti gli altri prodotti non terapeutici
  • Indicazioni terapeutiche:
  • Ribes Pet Symbio gatto è indicato per il benessere della cute e dell’intestino. A base di Olio di Ribes nero, Nucleotidi e Ossido di Zinco. Utile in caso di manifestazioni topiche ed intestinali, in regime di alimentazione controllata, in animali con permeabilità intestinale modificata, in animali con squilibri nel sistema immunitario, nei soggetti con una dimunuita tolleranza orale/mucosale.
  • Dettagli prodotto:
  • Posologia: Da somministrare al gatto direttamente in bocca o in aggiunta all’alimento completo in ragione di: 1 perla al dì fino a 5 kg di peso e di 2 perle per gatti con peso superiore ai 5 kg. È consigliabile somministrare Ribes Pet Symbio gatto per un periodo di 2 mesi.

Altre informazioni

Status

  • Fonte:
  • Ministero della Salute - Italia
  • Numero dell'autorizzazione:
  • 939757579
  • Ultimo aggiornamento:
  • 23-12-2017

Foglio illustrativo: composizione, posologia, indicazioni, interazioni, gravidanza, allattamento, effetti indesiderati, controindicazioni

RIBES PET SYMBIO GATTO

Mangime complementare per gatti a base di olio di ribes nero,nucleotidi e ossido di zinco.

Ribes Pet Symbio gatto è indicato per il benessere della cute e dell'intestino.Utile in caso di

manifestazioni topiche ed intestinali, in regime di alimentazionecontrollata, in animali con permeabilità

intestinale

modificata,

animali

consquilibri

sistema

immunitario.

Ingredienti

Oli e grassi vegetali (Ribes nigrum L. (58,30%), Lactobacillus reuteri NBF2*, gelatina (suino), glicerolo.

(*)inattivato

termicamente.

Additivi

(per

kg):

Composti di oligoelementi: 3b603 Zinco ossido mg 13.993 (Zn mg11.237), aromi naturali o

corrispondenti sintetici a struttura chimica definita: CAS No.352195-40-5 / disodio inosina-5-mono-

fosfato (IMP) mg 11.660; CAS No. 5550-12-9 / disodioguanosina 5'-monofosfato (GMP) mg 11.660.

Componenti analitici: umidità <0,5%, proteine gregge 15,89%, oli e grassi greggi58,40%, fibra greggia

0,02%,

ceneri

gregge

1,5%,

Omega

totali

min.

35%,

Omega

totalimin.

9,0%.

Apporto

nutrizionale.

Ogni perla contiene: olio di semi di ribes nero: 625 mg (acido linoleico 287,5 mg, acidogammalinolenico

87,5 mg, acido alfa-linolenico 84,5 mg, acido stearidonico 15 mg);Lactobacillus reuteri NBF 2*: 100 mg

(*)inattivato

termicamente;

nucleotidi(IMP+GMP):

Zinco:

Modalità

d'uso

Da somministrare al gatto direttamente in bocca o in aggiunta all'alimento completo inragione di: 1 perla

al dì fino a 5 kg di peso e di 2 perle per gatti con pesosuperiore ai 5 kg. È consigliabile somministrare

Ribes

Symbio

gatto

unperiodo

mesi.

Avvertenze

Da consumarsi preferibilmente entro la data indicata sul lato della confezione. Siraccomanda acqua a

volontà. Si raccomanda di chiedere il parere di un veterinarioprima dell'uso oppure prima di estendere il

periodo

impiego.

Conservazione

Conservare il prodotto in un luogo fresco, asciutto ed al riparo dalla luce diretta aduna temperatura non

superiore

25°

Formato

Confezione da 30 perle

17-1-2019

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Statement from FDA Commissioner Scott Gottlieb, M.D., on unprecedented new efforts to support development of over-the-counter naloxone to help reduce opioid overdose deaths

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Europe - EFSA - European Food Safety Authority EFSA Journal

24-12-2018

Columbia River Natural Pet Foods Inc. Voluntarily Expands Recall to Include Cow Pie and Chicken & Vegetables Fresh Frozen Meats for Dogs and Cats Due to Possible Health Risk

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Columbia River Natural Pet Foods of Vancouver, WA is voluntarily expanding their current recall to include additional products: 261 packages of Cow Pie Lot # 72618 and 82 packages of Chicken & Vegetables Lot# 111518 fresh frozen meats for dogs and cats, produced in July 2018 and November 2018, due to their potential to be contaminated with Salmonella and Listeria monocytogenes

FDA - U.S. Food and Drug Administration

20-12-2018

Data sources on animal diseases: Methodology on mapping the data sources on animal diseases in European Union Member States

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Europe - EFSA - European Food Safety Authority EFSA Journal

14-12-2018

Response to comments on the Scientific Opinion on the scientific substantiation of a health claim related to Symbiosal® and lowering of blood pressure and reduced risk of hypertension pursuant to Article 14 of Regulation (EC) No 1924/2006

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Published on: Thu, 13 Dec 2018 Following a request from the European Commission, EFSA was asked to review the comments received on the Scientific Opinion of the EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA) on the scientific substantiation of a health claim related to Symbiosal® and lowering of blood pressure and reduced risk of hypertension pursuant to Article 14 of Regulation (EC) No 1924/2006. Comments originating from the applicant (Han‐Biotech GmbH) were submitted to EFSA via the E...

Europe - EFSA - European Food Safety Authority Publications

13-12-2018

Pest categorisation of Septoria malagutii

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Europe - EFSA - European Food Safety Authority Publications

12-12-2018

Grant agreement for piloting the Framework Partnership Agreement between the National data provider organisations in France and EFSA – Final report

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Europe - EFSA - European Food Safety Authority Publications

5-12-2018

Columbia River Natural Pet Foods Inc. Recalls Cow Pie Fresh Frozen Meats for Dogs and Cats Because of Possible <em>Listeria monocytogenes</em> Health Risk

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Columbia River Natural Pet Foods of Vancouver, WA is voluntarily recalling 933 packages of Cow Pie fresh frozen meats for dogs and cats, produced in August 2017, because it has the potential to be contaminated with Listeria monocytogenes

FDA - U.S. Food and Drug Administration

3-12-2018

FDA Alerts Pet Owners about Potentially Toxic Levels of Vitamin D in Several Dry Pet Foods

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The FDA is investigating the presence of elevated, potentially toxic levels of vitamin D in several dry pet foodsVitamin D in very high amounts can cause serious health problems like kidney failure or death.

FDA - U.S. Food and Drug Administration

1-12-2018

Safety assessment of the process ‘RecyPET Hungária’, based on RecyPET Hungária technology, used to recycle post‐consumer PET into food contact materials

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Europe - EFSA - European Food Safety Authority Publications

29-11-2018

ELM Pet Foods Recall of Dry Dog Food Due to Elevated Levels of Vitamin D

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ELM Pet Foods, Inc is issuing a voluntary recall of Elm Chicken and Chickpea Recipe dog food because the products could contain elevated levels of Vitamin D.

FDA - U.S. Food and Drug Administration

28-11-2018

ANF Pet Inc. Issues Voluntary Precautionary Recall of Dry Dog Food Due to Potentially Elevated Levels of Vitamin D

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FDA - U.S. Food and Drug Administration

24-11-2018

The EFSA‐funded collection of dietary and related data in the general population aged 10‐74 years in Greece

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Europe - EFSA - European Food Safety Authority Publications

24-11-2018

Hazard identification and ranking for poultry at slaughter

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Published on: Fri, 23 Nov 2018 The Hellenic Health Foundation received support from the European Food Safety Authority in order to organise a national nutrition survey according to the methodology described in the EFSA Guidance document and to collect food consumption and related information among 780 adolescents, adults and elderly residing permanently in Greece. The EFSA‐funded data collection was largely based on the protocol of a large scale Greek national nutrition and health survey, called HYDRIA....

Europe - EFSA - European Food Safety Authority Publications

9-11-2018

Natural Life Pet Products Expands Recall of Dry Food Due to Elevated Levels of Vitamin D

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We regret to inform you that Natural Life® Chicken & Potato dry dog food has been confirmed to contain elevated levels of Vitamin D.

FDA - U.S. Food and Drug Administration

3-11-2018

Natural Life Pet Products Issues Recall of Dry Food Due to Elevated Levels of Vitamin D

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FDA - U.S. Food and Drug Administration

1-11-2018

Pest categorisation of Conotrachelus nenuphar

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Europe - EFSA - European Food Safety Authority Publications

31-10-2018

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Europe - EFSA - European Food Safety Authority Publications

17-10-2018

Pest categorisation of Stagonosporopsis andigena

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Europe - EFSA - European Food Safety Authority Publications

15-10-2018

October 11, 2018: Two Companies Ordered to Pay More Than $7 Million for Adulterated and Misbranded Pet Food Ingredients

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FDA - U.S. Food and Drug Administration

2-10-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on new agency actions to further deter ‘gaming’ of the generic drug approval process by the use of citizen petitions

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FDA - U.S. Food and Drug Administration

13-9-2018

Bravo Packing, Inc. Recalls Performance Dog Raw Pet Food Because of Possible Salmonella Health Risk to Humans and Animals

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FDA - U.S. Food and Drug Administration

11-9-2018

Radagast Pet Food, Inc. recalls various Rad Cat Raw Diet Pet Food

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The recalled pet food may be contaminated with Listeria monocytogenes and there is risk of cross contamination and illness after handling the pet food.

Health Canada

1-9-2018

Multiple “Dr. King’s” homeopathic and “Natural Pet” veterinary products recalled due to potential microbial contamination

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Health Canada

29-8-2018

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Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Safety assessment of the process ‘General Plastic’, based on Starlinger Decon technology, used to recycle post‐consumer PET into food contact materials

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Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Grant agreement for piloting the Framework Partnership Agreement between the National data provider organisations in Slovakia and EFSA – Final report

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Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Strategic partnership with German data providing institutions on data quality (Pilot project) – Final report

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Europe - EFSA - European Food Safety Authority Publications

28-8-2018

FDA alerts consumers, pet owners not to use products manufactured by King Bio, including Dr. King’s label, homeopathic drug and pet products

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FDA - U.S. Food and Drug Administration

22-8-2018

Radagast Pet Food Voluntarily Expands Recall to Include Rad Cat Raw Diet Products With Best By Dates of 10/19/18 Through 12/3/19 Due to Potential Health Risk

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Radagast Pet Food, Inc. of Portland, OR is expanding its voluntary recall to include an additional quantity of Rad Cat Raw Diet across all varieties with Best By dates of 10/19/18 through 12/3/19 because it has the potential to be contaminated with Listeria monocytogenes. Radagast Pet Food is conducting this voluntary recall out of an abundance of caution because of its strong commitment to food safety and quality.

FDA - U.S. Food and Drug Administration

6-8-2018

G & C Raw, LLC Recalls Pat's Cat Turkey, and Ground Lamb Pet Food, because of Possible Listeria Monocytogenes Health Risk

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FDA - U.S. Food and Drug Administration

19-7-2018

Radagast Pet Food Inc. recalls Rad Cat Raw Diet Free-Range Pet Food

Radagast Pet Food Inc. recalls Rad Cat Raw Diet Free-Range Pet Food

The pet food may be contaminated with Listeria monocytogenes and there is risk of cross contamination and illness after handling the pet food.

Health Canada

19-7-2018

K9 Natural Ltd recalls K9 Natural Frozen Chicken Feast Raw Pet Food 11lb bags

K9 Natural Ltd recalls K9 Natural Frozen Chicken Feast Raw Pet Food 11lb bags

K9 Natural Ltd is voluntarily recalling K9 Natural Frozen Chicken Feast 11lb bags, batch number #150517, that were imported into the Canadian market in July 2017 because they have the potential to be contaminated with Listeria monocytogenes. No other K9 Natural products are affected in Canada.

Health Canada

17-7-2018

Statement from FDA Commissioner Scott Gottlieb, M.D. on new efforts to empower consumers by advancing access to nonprescription drugs

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FDA - U.S. Food and Drug Administration

12-7-2018

FDA Investigating Potential Connection Between Diet and Cases of Canine Heart Disease

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FDA is alerting pet owners and veterinary professionals about reports of canine dilated cardiomyopathy (DCM) in dogs eating certain pet foods containing peas, lentils, other legume seeds, or potatoes as main ingredients.

FDA - U.S. Food and Drug Administration

6-7-2018

Radagast Pet Food, Inc. Voluntarily Recalls Three Lots of Rad Cat Raw Diet Free-Range Chicken Recipe and One Lot of Pasture-Raised Venison Recipe Because of Possible Health Risk

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Radagast Pet Food, Inc. of Portland, OR is recalling three lots of Rad Cat Raw Diet Free-Range Chicken Recipe because testing results indicate they have the potential to be contaminated with Listeria monocytogenes. The Company is also recalling one lot of Rad Cat Raw Diet Pasture-Raised Venison Recipe because testing results indicate it has the potential to be contaminated with Shiga Toxin producing E. coli O121. This recall is being conducted out of an abundance of caution. Due to Radagast Pet Food’s ...

FDA - U.S. Food and Drug Administration

21-6-2018

Carenza Petinimid (etosuccimide) - modalità di richiesta d'importazione dall'estero (21/06/2018)

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L'Agenzia Italiana del Farmaco rende disponibili aggiornamenti relativi al medicinale "Petinimid (Etosuccimide)", non reperibile sul territorio nazionale per il quale è stata autorizzata l’importazione dall’estero su richiesta dell’azienda.

Italia - AIFA - Agenzia Italiana del Farmaco

12-6-2018

Dave’s Pet Food Voluntarily Recalls 95% Premium Beef Canned Dog Food Due to Potentially Elevated Levels of Thyroid Hormone

Dave’s Pet Food Voluntarily Recalls 95% Premium Beef Canned Dog Food Due to Potentially Elevated Levels of Thyroid Hormone

Dave’s Pet Food of Agawam, MA is recalling a single lot of Dave’s Dog Food 95% premium beef cans because the products potentially contain elevated levels of beef thyroid hormone.

FDA - U.S. Food and Drug Administration

24-5-2018

Ticks and Lyme Disease: Symptoms, Treatment, and Prevention

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Lyme disease is on the rise. How can you prevent it? What are the symptoms, and what should you do if you think you or your pet have it?

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

11-5-2018

May 10, 2018: South Carolina Couple Sentenced to a Total of 138 Months in Prison for Trafficking Counterfeit Goods, Including Misbranded Pet Medicine

May 10, 2018: South Carolina Couple Sentenced to a Total of 138 Months in Prison for Trafficking Counterfeit Goods, Including Misbranded Pet Medicine

May 10, 2018: South Carolina Couple Sentenced to a Total of 138 Months in Prison for Trafficking Counterfeit Goods, Including Misbranded Pet Medicine

FDA - U.S. Food and Drug Administration

15-8-2018

Scientific guideline:  Draft guideline on quality of herbal medicinal products/traditional herbal medicinal products - Revision 3 , draft: consultation open

Scientific guideline: Draft guideline on quality of herbal medicinal products/traditional herbal medicinal products - Revision 3 , draft: consultation open

This document intends to cover the general quality aspects of herbal medicinal products for human and veterinary use, including traditional herbal medicinal products for human use. It describes the special problems of herbal medicinal products and the differences between medicinal products containing chemically defined active substances.

Europe - EMA - European Medicines Agency

26-7-2018

Regulatory and procedural guideline:  EudraVigilance release notes v.1.17

Regulatory and procedural guideline: EudraVigilance release notes v.1.17

This document lists and briefly describes the following areas for the releases of EVWEB starting with the release on 22 November 2017.

Europe - EMA - European Medicines Agency

15-6-2018

Regulatory and procedural guideline:  EudraVigilance release notes v.1.15

Regulatory and procedural guideline: EudraVigilance release notes v.1.15

This document lists and briefly describes the following areas for the releases of EVWEB starting with the release on 22 November 2017.

Europe - EMA - European Medicines Agency

24-5-2018

Regulatory and procedural guideline:  EudraVigilance release notes v.1.14

Regulatory and procedural guideline: EudraVigilance release notes v.1.14

This document lists and briefly describes the following areas for the releases of EVWEB starting with the release on 22 November 2017.

Europe - EMA - European Medicines Agency

23-5-2018

Scientific guideline:  Draft guideline on the responsibilities of the sponsor with regard to handling and shipping of investigational medicinal products for human use in accordance with good clinical practice and good manufacturing practice, draft: consul

Scientific guideline: Draft guideline on the responsibilities of the sponsor with regard to handling and shipping of investigational medicinal products for human use in accordance with good clinical practice and good manufacturing practice, draft: consul

The guideline lays down the principles for the two-step release and shipping of the investigational medicinal products by the qualified person and the sponsor. The guideline also describes the areas of interface between the manufacturer and the sponsor and the required contractual agreements.

Europe - EMA - European Medicines Agency