ALIVIHO – REUMA

Información principal

  • Denominación comercial:
  • ALIVIHO – REUMA gotas sublinguales
  • formulario farmacéutico:
  • Gotas sublinguales
  • Usar para:
  • Humanos
  • Tipo de medicina:
  • medicamento alopático

Documentos

  • para el público en general:
  • El prospecto de información de este producto no está disponible actualmente, puede enviar una petición a nuestro servicio al cliente y le notificaremos tan pronto como nos sea posible para conseguirlo.


    Solicitar el prospecto de información al público.

Localización

  • Disponible en:
  • ALIVIHO – REUMA  gotas sublinguales
    Cuba
  • Idioma:
  • español

Otros datos

Estado

  • Fuente:
  • CECMED - Autoridad Reguladora de Medicamentos, Equipos y Dispositivos Médicos - Cuba
  • Número de autorización:
  • h18021-v03
  • última actualización:
  • 10-05-2018

Ficha Técnica

RESUMEN DE LAS CARACTERISTICAS DEL PRODUCTO HOMEOPÁTICO

Nombre del producto: ALIVIHO®– REUMA, gotas sublinguales

Origen del material de partida: Vegetal, animal y mineral.

Forma farmacéutica: Gotas sublinguales

Grado de dilución o potenciación: 9-30 CH

Presentación: Estuche por un frasco de vidrio ámbar con tapa-gotero de PP con 15 ó 30

Titular, país: GRUPO EMPRESARIAL DE PRODUCCIONES BIOFARMACÉUTICAS Y

QUÍMICAS. LABIOFAM, La Habana, Cuba.

Fabricante, país: EMPRESA LABIOFAM CIENFUEGOS. UNIDAD EMPRESARIAL DE

BASE PRODUCCIONES FARMACÉUTICAS Y VETERINARIAS (UEB) LABORATORIO DE

HOMEOPATÍA, Cienfuegos, Cuba.

Número de Registro Sanitario: H-18-021-V03

Fecha de Inscripción: 6 de marzo de 2018

Material de partida: Aconitum napellus 15 CH, Asclepias tuberosa 15 CH, Colchicum

automnale 9 CH, Solanum dulcamara 15 CH, Ferrum phosphoricum 12 CH, Formica rufa 9

CH, Phytolacca decandra 30 CH, Rhus toxicodendron 30 CH, Sticta pulmonaria 12 CH.

Plazo de validez: 24 meses

Condiciones de almacenamiento:

Protéjase de la luz. No refrigerar. Mantenga el frasco dentro del estuche.

Usos recomendados: Medicamento Homeopático utilizado como tratamiento auxiliar para

procesos inflamatorios agudos y crónicos incluyendo inflamaciones musculares agudas,

reumatismo, artritis y artrosis. La acción clínica de cada componente para esta indicación es

la siguiente:

Contraindicaciones:

Hipersensibilidad al medicamento o a sus componentes.

Precauciones:

El uso de este producto no excluye, sustituye o limita la aplicación de otros tratamientos.

Este producto contiene etanol al 30 %, por lo que en niños menores de 10 años, embarazo,

lactancia,

geriatría

personas

sensibles

(desórdenes

hepáticos

alcoholismo),

recomendamos diluirlo en ¼ vaso de agua.

Advertencias especiales y precauciones de uso:

No manipular o administrar este producto en presencia de olores fuertes (perfume, tabaco,

ambientadores, mentol, desinfectantes, etc.). No administrar junto con comidas o bebidas.

Se recomienda, no fumar, beber, comer o lavarse los dientes 20 minutos antes y después

administración.

Mantener

alejado

equipos

electrónicos

generen

ondas

electromagnéticas

fuertes

(televisores,

microondas,

computadoras,

celulares,

radios,

teléfonos inalámbricos, refrigeradores, etc). En caso de aparición de síntomas severos

asociados a los usos recomendados u otros signos no relacionados, se debe acudir al

médico.

Efectos indeseables:

No se han reportado hasta la fecha.

Posología y modo de administración:

Se recomienda la administración de una dosis (5 gotas) 4 veces al día durante al menos 5

días. En caso de agudización de los síntomas, puede administrarse una dosis (5 gotas) cada

1 h y luego, en la medida en que se alcance la mejoría, disminuir gradualmente la frecuencia

hasta la posología recomendada de 4 dosis diarias. Se recomienda no exceder los 21 días

de tratamiento. Durante el tratamiento deben respetarse los horarios de sueño.

Interacciones con otros productos medicinales y otras formas de interacción:

No se han reportado hasta la fecha.

Componente

Coadyuva al alivio de:

Aconitum napellus

Dolor agudo

Asclepias tuberosa

Inflamaciones, dolores reumáticos

Colchicum automnale

Artritis reumatoide, inflamación de articulaciones

Solanum dulcamara

Dolores articulares, contracturas musculares

Ferrum phosphoricum

Entumecimiento, flujo sanguíneo restringido

Formica rufa

Dolor reumático, articulaciones rígidas y contracturadas,

nudosidades artríticas

Phytolacca decandra

Artritis reumatoide, dolores reumáticos, inflamación crónica

Rhus toxicodendron

Artritis, reuma con rigidez dolorosa

Sticta pulmonaria

Dolores crónicos

Uso en embarazo y lactancia.

Este

producto

contiene

etanol

niños

menores

de 10

años,

embarazo,

lactancia,

geriatría

personas

sensibles

(desórdenes

hepáticos

alcoholismo), recomendamos diluirlo en ¼ vaso de agua.

Efectos sobre la conducción de vehículos / maquinaria:

No se han reportado hasta la fecha,

Sobredosis:

Medidas generales..

Otras propiedades atribuidas o demostradas.

No se han reportado hasta la fecha.

Instrucciones de uso y manipulación del producto.

Antes de administrar cada dosis se sugiere golpear al menos 10 veces el frasco contra la

palma de la mano. Se recomienda la administración sublingual con la boca completamente

limpia y libre de olores fuertes y cualquier sabor. Por lo que no se debe comer, beber,

cepillarse los dientes ni fumar 20 minutos antes o después de la administración del

medicamento. En caso de administrar el producto diluido en agua potable (1/4 vaso), este se

debe retener en la boca durante 5 segundos garantizando el contacto sublingual. Se

recomienda

además

evitar

contacto

cuentagotas,

interior

tapa

medicamento con las manos o labios. Se sugiere dispensar previamente cada dosis (5

gotas) en la tapa del frasco y luego administrar debajo de la lengua.

Fecha de aprobación/revisión del texto: 6 de marzo de 2018

  • El prospecto de información de este producto no está disponible actualmente, puede enviar una petición a nuestro servicio al cliente y le notificaremos tan pronto como nos sea posible para conseguirlo.

    Solicitar el prospecto de información al público.



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Livestock Health and Food Chain Risk Assessment

Livestock Health and Food Chain Risk Assessment

Published on: Mon, 27 Aug 2018 00:00:00 +0200 The EUFORA fellowship programme ‘Livestock Health and Food Chain Risk Assessment’ was proposed by the Animal and Plant Health Agency (APHA), a British governmental institution responsible for safeguarding animal and plant health in the UK. The working programme, which was organised into four different modules, covered a wide range of aspects related to risk assessment including identification of emerging risks, risk prioritisation methods, scanning surveilla...

Europe - EFSA - European Food Safety Authority Publications

10-9-2018

USDA and FDA announce joint public meeting on use of animal cell culture technology to develop products derived from livestock and poultry

USDA and FDA announce joint public meeting on use of animal cell culture technology to develop products derived from livestock and poultry

WASHINGTON, Sept. 10, 2018 – U.S. Secretary of Agriculture Sonny Perdue, DVM and U.S. Food and Drug Administration Commissioner Scott Gottlieb, M.D. today announced a joint public meeting to be held on Oct. 23-24, 2018 to discuss the use of cell culture technology to develop products derived from livestock and poultry.

FDA - U.S. Food and Drug Administration

29-8-2018

Risk to human and animal health related to the presence of 4,15‐diacetoxyscirpenol in food and feed

Risk to human and animal health related to the presence of 4,15‐diacetoxyscirpenol in food and feed

Published on: Thu, 16 Aug 2018 00:00:00 +0200 4,15‐Diacetoxyscirpenol (DAS) is a mycotoxin primarily produced by Fusarium fungi and occurring predominantly in cereal grains. As requested by the European Commission, the EFSA Panel on Contaminants in the Food Chain (CONTAM) assessed the risk of DAS to human and animal health related to its presence in food and feed. Very limited information was available on toxicity and on toxicokinetics in experimental and farm animals. Due to the limitations in the avai...

Europe - EFSA - European Food Safety Authority Publications

28-8-2018

King Bio Issues Voluntary Nationwide Recall of All Aqueous-Based Products for Human and Animal Use Due to Possible Microbial Contamination

King Bio Issues Voluntary Nationwide Recall of All Aqueous-Based Products for Human and Animal Use Due to Possible Microbial Contamination

King Bio is voluntarily recalling all of its aqueous-based products for human and animal use (see website link below), within expiry, to the consumer level due to possible microbial contamination.

FDA - U.S. Food and Drug Administration

22-8-2018

Santevia Water System Inc. recalls PureEasy Shower Filter

Santevia Water System Inc. recalls PureEasy Shower Filter

The housing can unexpectedly separate releasing the mineral contents into the eyes.

Health Canada

17-8-2018

Animal Drug Under Fee Amendments Reauthorized Through September 2023 to Allow for FDA’s Continued Timely Review of Animal Drug Applications

Animal Drug Under Fee Amendments Reauthorized Through September 2023 to Allow for FDA’s Continued Timely Review of Animal Drug Applications

On 8/14/18, the Animal Drug and Animal Generic Drug User Fee Amendments of 2018 was signed into law to reauthorize ADUFA and AGDUFA. These programs help FDA maintain a predictable and timely animal drug review process, foster innovation, and expedite access to new therapies for animals.

FDA - U.S. Food and Drug Administration

15-8-2018

Statement by FDA Commissioner Scott Gottlieb, M.D., on the FDA’s new resource guide to support responsible opioid prescribing for pain management in animals

Statement by FDA Commissioner Scott Gottlieb, M.D., on the FDA’s new resource guide to support responsible opioid prescribing for pain management in animals

Statement by FDA Commissioner Scott Gottlieb, M.D., on the FDA’s new resource guide in support of responsible opioid prescribing for safe, effective pain management in animals

FDA - U.S. Food and Drug Administration

7-8-2018

FDA’s Center for Veterinary Medicine Announces Second eSubmitter Webinar in Ongoing Series

FDA’s Center for Veterinary Medicine Announces Second eSubmitter Webinar in Ongoing Series

On August 22, 2018, FDA-CVM will host the second of a three-part webinar series on using eSubmitter, CVM’s electronic submission tool for the animal drug approval process. Sponsors must use eSubmitter to submit applications as of October 1, 2018.

FDA - U.S. Food and Drug Administration

6-8-2018

Current Animal Food GRAS Notices Inventory

Current Animal Food GRAS Notices Inventory

Listing of current Animal Food GRAS notices including notifier, substance, intended use, intended species, and FDA’s response.

FDA - U.S. Food and Drug Administration

31-7-2018

ADM Animal Nutrition Recalls Mintrate® 36-15 Breed Right Cattle Tub - A specific lot of product may contain elevated levels of non-protein nitrogen, could harm cattle

ADM Animal Nutrition Recalls Mintrate® 36-15 Breed Right Cattle Tub - A specific lot of product may contain elevated levels of non-protein nitrogen, could harm cattle

ADM Animal Nutrition, a division of Archer Daniels Midland Company (NYSE: ADM), is recalling 200-pound tubs of Mintrate® 36-15 Breed Right Tub cattle feed, product number 54549AAA6H, because the product may contain elevated levels of non-protein nitrogen, which could be harmful to cattle. Excessive levels of non-protein nitrogen can be toxic to cattle and can cause muscle tremors (especially of face and ears), abdominal pain, bloat, frothy salivation, excessive urination, teeth grinding, incoordination, ...

FDA - U.S. Food and Drug Administration

29-6-2018

UPDATE: FDA Animal Drug Safety Communication: FDA continues to warn about risk of accidental overdosing of dogs with the noise aversion drug Sileo

UPDATE: FDA Animal Drug Safety Communication: FDA continues to warn about risk of accidental overdosing of dogs with the noise aversion drug Sileo

FDA is alerting dog owners and veterinarians about the risk of accidental overdose to dogs treated with the drug Sileo, a prescription gel that is given to dogs by mouth to treat noise aversion.

FDA - U.S. Food and Drug Administration

28-6-2018

FDA Releases Guidance to Help Animal Drug Sponsors with Antimicrobial Animal Drug Sales and Distribution Reporting Requirements

FDA Releases Guidance to Help Animal Drug Sponsors with Antimicrobial Animal Drug Sales and Distribution Reporting Requirements

FDA is releasing Guidance for Industry #252. This small entity compliance guide is intended to help small businesses comply with the Antimicrobial Animal Drug Sales and Distribution final rule.

FDA - U.S. Food and Drug Administration

20-6-2018

Signature of the framework agreement for the ESA Platform: strengthening epidemiological surveillance in animal health

Signature of the framework agreement for the ESA Platform: strengthening epidemiological surveillance in animal health

The signing of the new framework agreement for the Epidemiological Surveillance Platform for Animal Health (ESA Platform) on 20 June 2018 by the Director General for Food in the presence of Roger Genet, Director General of ANSES, and eight other members, signals a new departure for this platform, which has demonstrated its usefulness and effectiveness ever since it was set up in October 2011.  

France - Agence Nationale du Médicament Vétérinaire

14-6-2018

FDA Releases FSMA Draft Guidance on the Supply-Chain Program Preventive Control for Animal Food

FDA Releases FSMA Draft Guidance on the Supply-Chain Program Preventive Control for Animal Food

FDA issued draft guidance to help animal food facilities needing a supply-chain program meet those requirements under the Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Food for Animals rule.

FDA - U.S. Food and Drug Administration

7-6-2018

Ovejoterapia: la nueva metodología que impacta física y cognitivamente en personas con discapacidad

Ovejoterapia: la nueva metodología que impacta física y cognitivamente en personas con discapacidad

“Las ovejas son una especie altamente social, superinteligentes, y son animales muy poco agresivos, por eso considerábamos que cumplían con requisitos mínimos para trabajar con niños en terapia, fue así como se nos ocurrió incluirlas en el trabajo terapéutico”, relata María José Ubilla, veterinaria, etóloga y coordinadora del Centro de Terapia Asistidas con Animales (CTAA) […]

Cuba - infomed - Red de Salud de Cuba

25-5-2018

Food Safety Modernization Act and Animal Feed

Food Safety Modernization Act and Animal Feed

This page highlights FSMA content that will be of most interest to manufacturers and distributors of animal food.

FDA - U.S. Food and Drug Administration

24-5-2018

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

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

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

24-5-2018

Three questions for Gilles Salvat, ANSES Managing Director General for Research and Reference

Three questions for Gilles Salvat, ANSES Managing Director General for Research and Reference

As Reference Delegation Day is held at ANSES, bringing together representatives of national and European reference laboratories, Gilles Salvat, Managing Director General for Research and Reference, gives us an overview of this essential part of ANSES's work. What do you mean by reference? Reference is an essential component of the system for safeguarding health. The work of the reference laboratories is vital to improving knowledge and identification of the major hazards we face in food safety, animal...

France - Agence Nationale du Médicament Vétérinaire

19-10-2018

Recocam (Bimeda Animal Health Limited)

Recocam (Bimeda Animal Health Limited)

Recocam (Active substance: Meloxicam) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6954 of Fri, 19 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/2247/T/10

Europe -DG Health and Food Safety

21-9-2018

Scientific guideline:  Reflection paper on the use of aminopenicillins and their beta-lactamase inhibitor combinations in animals in the European Union: development of resistance and impact on human and animal health, draft: consultation open

Scientific guideline: Reflection paper on the use of aminopenicillins and their beta-lactamase inhibitor combinations in animals in the European Union: development of resistance and impact on human and animal health, draft: consultation open

The objective of this document is to review available information on the use of aminopenicillins and their beta-lactamase inhibitor combinations in veterinary medicines in the EU, their effect on the emergence of antimicrobial resistance (AMR) and the potential impact of resistance on human and animal health. The document provides information for the risk profiling, as recommended by the Antimicrobial Advice ad hoc Expert Group (AMEG) of the EMA.

Europe - EMA - European Medicines Agency

11-9-2018

 Focus group meeting  on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics harmonisation, European Medicines Agency, London, UK, From: 12-Oct-2018, To: 12-Oct-2018

Focus group meeting on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics harmonisation, European Medicines Agency, London, UK, From: 12-Oct-2018, To: 12-Oct-2018

This meeting will allow a direct exchange of views between the Agency’s working party and stakeholders on its draft reflection paper on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics (SPC) harmonisation (EMA/CVMP/849775/2017). It complements the public consultation on this reflection paper ending on 31 January 2019. The reflection paper follows considerations in the report on a pilot project that aimed to develop and test non-experimental appr...

Europe - EMA - European Medicines Agency

27-7-2018

Scientific guideline:  Reflection paper on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics (SPC) harmonisation, draft: consultation open

Scientific guideline: Reflection paper on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics (SPC) harmonisation, draft: consultation open

Established veterinary antibiotics are not always used at the authorised dose, and the dose may need to be reviewed in order to maintain their effectiveness whilst limiting the risks of antimicrobial resistance. Before a new dose is introduced, the company would typically have to conduct new studies to ensure it does not negatively affect the safety of the target animal, the consumer of animal produce, or the environment. This may reduce product availability, which could have a negative impact on antimic...

Europe - EMA - European Medicines Agency

16-7-2018

Procox (Bayer Animal Health GmbH)

Procox (Bayer Animal Health GmbH)

Procox (Active substance: emodepside and toltrazuril) - Centralised - Yearly update - Commission Decision (2018)4753 of Mon, 16 Jul 2018

Europe -DG Health and Food Safety

13-6-2018

Veraflox (Bayer Animal Health GmbH)

Veraflox (Bayer Animal Health GmbH)

Veraflox (Active substance: Pradofloxacin) - Centralised - Yearly update - Commission Decision (2018)3834 of Wed, 13 Jun 2018

Europe -DG Health and Food Safety

29-5-2018

Profender (Bayer Animal Health GmbH)

Profender (Bayer Animal Health GmbH)

Profender (Active substance: Emodepside / Praziquantel) - Centralised - Yearly update - Commission Decision (2018)3405 of Tue, 29 May 2018

Europe -DG Health and Food Safety