Ensure

Glavne informacije

  • Zaščiteno ime:
  • Ensure vanilija 250 ml pločevinka
  • Farmacevtska oblika:
  • peroralna suspenzija
  • Sestava:
  • živilo za posebne zdravstvene namene 250 ml / 1 pločevinka
  • Pot uporabe:
  • Peroralna uporaba
  • Enote v paketu:
  • 250 ml pločevinka
  • Uporabi za:
  • ljudje
  • Vrsta medicine:
  • Alopatska drog

Dokumentov

Lokalizacija

  • Na voljo v:
  • Ensure vanilija 250 ml pločevinka
    Slovenija
  • Jezik:
  • slovenščina

Terapevtski podatki

  • Terapevtska skupina:
  • Maščobe, ogljikovi hidrati, proteini, minerali in vitamini, kombinacije

Drugi podatki

Stanje

  • Source:
  • JAZMP - Javna agencija RS za zdravila in medicinske pripomočke - Slovenia Medicines Agency
  • Status dovoljenje:
  • Živilo
  • Zadnja posodobitev:
  • 19-01-2018

Podatki za bolnike

ŽIVILO ZA POSEBNE ZDRAVSTVENE NAMENE

Uporaba samo pod zdravniškim nadzorom

Popolno in uravnoteženo živilo

ENSURE

®

okus: vanilija

1,0 kcal/ml

250 ml

PRIPOROČENO ODMERJANJE: Kot edini vir prehrane 6-7 pakiranj/dan, kot dopolnilna

prehrana 2–3 pakiranji/dan.

NAVODILO

ZA

UPORABO:

ENSURE®

pripravljen

uporabo.

DOBRO

PRETRESITE.

Pločevinko

odprite

pred

uporabo.

odprtju

shranjujte

pokrito

pločevinko v hladilnikuin uporabite v roku 24 ur. Po tem času je ostanek potrebno

zavreči.

POMEMBNO OBVESTILO: ENSURE® je primeren kot edini vir prehrane ali kot dodatek

k prehrani in se mora uporabljati pod zdravniškim nadzorom. Ni namenjen za uporabo

pri otrocih, razen če to priporoči zdravnik ali drug usposobljen zdravstveni delavec. Ni

primeren

osebe

galaktozemijo.

PARENTERALNO

(INTRAVENSKO)

UPORABO.

SHRANJEVANJE: Neodprto pločevinko shranjujte pri sobni temperaturi.

Uporabno najmanj do konca: označeno na originalni ovojnini

Izdelovalec: Abbott Laboratories B.V., Zwolle, Nizozemska

PAKIRANO V KONTROLIRANI ATMOSFERI

Sestavine:

voda,

hidroliziran

koruzni

škrob,

kalcijev

natrijev

kazeinat

(mlečne

beljakovine), saharoza, olje repičnega semena, sončnično olje z visoko vsebnostjo

oleinske kisline, MINERALI (kalijev citrat, magnezijev klorid, natrijev citrat, kalcijev fosfat,

kalijev klorid, kalijev hidrogenfosfat, železov sulfat, cinkov sulfat, manganov sulfat,

bakrov sulfat, natrijev molibdat, natrijev selenat, kromov klorid, kalijev jodid), izolat

sojinih

beljakovin,

koruzno

olje,

aroma,

emulgator:

E322

(sojin

lecitin),

VITAMINI

(holinijev

klorid,

askorbinska

kislina,

dl-alfa

tokoferilacetat,

niacinamid,

kalcijev

pantotenat, vitamin A palmitat, piridoksinijev klorid, tiaminijev klorid, riboflavin, folna

kislina, biotin, filokinon, vitamin D3, cianokobalamin), stabilizator: E407.

KOLIČINSKA SESTAVA

VSEBNOST

Enota

na 100 ml

ENERGIJSKA VREDNOST

kcal

beljakovine

4,00

maščobe

3,36

od teh nasičene maščobne kisline

ogljikovi hidrati

13,56

od teh sladkorji

voda

85,1

0,22

VITAMINI

vitamin A (palmitat)

μg RE

vitamin D

0,73

vitamin E

mg αTE

vitamin K

vitamin C

folna kislina

vitamin B

0,16

vitamin B

0,18

vitamin B

0,22

vitamin B

0,34

niacin

mg NE

pantotenska kislina

0,78

biotin

holin

MINERALI

natrij

kalij

klorid

kalcij

fosfor

magnezij

železo

cink

mangan

0,35

baker

selen

krom

molibden

osmolarnost

mOsm/L

9-11-2018

FDA seizes food and medical products held under insanitary conditions at an Arkansas grocery warehouse

FDA seizes food and medical products held under insanitary conditions at an Arkansas grocery warehouse

U.S. Marshals Service has conducted a mass seizure of FDA-regulated products that were being held in an Arkansas grocery warehouse under insanitary conditions

FDA - U.S. Food and Drug Administration

9-11-2018

Safety assessment of the substance Ln 1,4‐benzene dicarboxylic acid (with Ln = La, Eu, Gd, Tb) for use in food contact materials

Safety assessment of the substance Ln 1,4‐benzene dicarboxylic acid (with Ln = La, Eu, Gd, Tb) for use in food contact materials

Published on: Wed, 07 Nov 2018 00:00:00 +0100 The EFSA Panel on Food Contact Materials, Enzymes and Processing Aids (CEP Panel) assessed the safety of the additive Ln 1,4‐benzene dicarboxylic acid (with Ln = La, Eu, Gd, Tb) for use in food contact materials. It is a family of mixtures combining the four lanthanides lanthanum (La), europium (Eu), gadolinium (Gd) and/or terbium (Tb) in different proportions as their 1,4‐benzene dicarboxylate complexes, used as a taggant in plastics for authentication and ...

Europe - EFSA - European Food Safety Authority Publications

6-11-2018

Izzivi krepitve sistemov primarnega zdravstvenega varstva v regiji jugovzhodne Evrope

Izzivi krepitve sistemov primarnega zdravstvenega varstva v regiji jugovzhodne Evrope

Ministrstvo za zdravje, v sodelovanju z Nacionalnim inštitutom za javno zdravje, Zdravstveno mrežo...

Ministrstvo za zdravje

29-10-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on the FDA’s new consideration of labeling for sesame allergies

Statement from FDA Commissioner Scott Gottlieb, M.D., on the FDA’s new consideration of labeling for sesame allergies

Food allergies have touched the lives of most of us. Thousands of Americans experience life-threatening, food-related reactions each year, and an estimated 20 people die from them annually. In some cases, such reactions occur despite a careful reading of packaged food labels by conscientious consumers. To me, that’s unacceptable. The FDA is committed to advancing our efforts to help ensure that Americans have access to the information they need about common allergens in packaged foods.

FDA - U.S. Food and Drug Administration

26-10-2018

Državna sekretarka mag. Pia Vračko se je udeležila Globalne konference o primarnem zdravstvenem varstvu

Državna sekretarka mag. Pia Vračko se je udeležila Globalne konference o primarnem zdravstvenem varstvu

Državna sekretarka Ministrstva za zdravje mag. Pia Vračko se je udeležila Globalne konference o...

Ministrstvo za zdravje

24-10-2018

Sirob Imports, Inc. Issues Recall Due to Elevated Lead in Spices

Sirob Imports, Inc. Issues Recall Due to Elevated Lead in Spices

Sirob Imports, Inc of Lindenhurst, NY is recalling, Corrado, Orlando Imports, Nouri’s Syrian Bakery, Mediterranean Specialty Foods Brand and Butera Fruit Market Curry Powder because it contains elevated levels of lead.

FDA - U.S. Food and Drug Administration

11-10-2018

Minister za zdravje na 90. obletnici ZD Celje

Minister za zdravje na 90. obletnici ZD Celje

Minister za zdravje Samo Fakin se je danes udeležil 90. obletnice Zdravstvenega doma Celje. Na...

Ministrstvo za zdravje

4-10-2018

Odziv na ukinitev osebnega recepta za zdravnike brez licence in specializante

Odziv na ukinitev osebnega recepta za zdravnike brez licence in specializante

Minister za zdravje Samo Fakin je na vodstvo Zavoda za zdravstveno zavarovanje Slovenije (ZZZS)...

Ministrstvo za zdravje

28-9-2018

Drug agency from China visits Denmark

Drug agency from China visits Denmark

A delegation from the Centre for Drug Evaluation under the China National Medical Products Administration visited the Danish Medicines Agency this week to discuss clinical trials and drug monitoring, among other things. The meeting at the Danish Medicines Agency is part of a Danish-Chinese collaboration under the auspices of the China-Denmark Food and Drug Regulatory Cooperation Centre, which was established with the signing of a collaboration agreement in May of last year, and which aims to strengthen r...

Danish Medicines Agency

12-9-2018

Natural Disaster Preparedness and Response (Drugs)

Natural Disaster Preparedness and Response (Drugs)

The FDA reminds consumers to have an emergency plan and to take precautions for storing water and ensuring the safety of their food and medical supplies for themselves and their pets during and after severe storms (tornados, hurricanes, blizzards) and other events that can result in power outages, flooding, or road and business closures.

FDA - U.S. Food and Drug Administration

11-9-2018

Risk assessment of white willow (Salix alba) in food

Risk assessment of white willow (Salix alba) in food

Published on: Tue, 28 Aug 2018 00:00:00 +0200 This Technical Report contains a description of the activities within the work programme of the EU‐FORA Fellowship on the risk assessment of white willow in food. The bark of different varieties of willow has had a long history of medical use as a means to reduce fever and as a painkiller. Willow bark is also used in weight loss and sports performance food supplements. The labelling of these products usually does not mention any restrictions to the length of...

Europe - EFSA - European Food Safety Authority Publications

11-9-2018

Assessment of occupational and dietary exposure to pesticide residues

Assessment of occupational and dietary exposure to pesticide residues

Published on: Mon, 27 Aug 2018 00:00:00 +0200 Plant protection products (PPPs) are pesticides containing at least one active substance that drives specific actions against pests (diseases). PPPs are regulated in the EU and cannot be placed on the market or used without prior authorisation. EFSA assesses the possible risks of the use of active substances to humans and environment. Member States decide whether or not to approve their use at EU level. Furthermore, Member States decide at national level on ...

Europe - EFSA - European Food Safety Authority Publications

30-8-2018

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

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

Published on: Tue, 07 Aug 2018 00:00:00 +0200 Cyprus alongside with another 4 countries has participated successfully in the Grant Agreement GP/EFSA/DATA/2016/01‐GA 02, entitled: “Strategic Partnership with Cyprus on Data Quality”. The project was co‐financed by EFSA, aiming to help both EFSA and data providers from Member States to possess data of high quality in a quantitatively manageable way. The main objective of the grant agreement was the establishment of the data governance, coordination and imp...

Europe - EFSA - European Food Safety Authority Publications

30-8-2018

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

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

Published on: Tue, 07 Aug 2018 00:00:00 +0200 During the project seven standard operating procedures (SOP) were developed for the four data domains (zoonoses, chemical contaminant, pesticide residues and veterinary medical products residues). The SOPs describe 1) How the national governance of risk assessment data is organised, 2) how data are collected and validated before delivering to EFSA covering all four domains, 3) How data is transferred to EFSA, 4) how to respond to EFSA request for clarificati...

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

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

Published on: Fri, 10 Aug 2018 00:00:00 +0200 This scientific opinion of the EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF Panel) deals with the safety evaluation of the recycling process General Plastic (EU register No RECYC153), which is based on the Starlinger Decon technology. The decontamination efficiency of the process was demonstrated by a challenge test. The input of this process is hot caustic washed and dried poly(ethylene terephthalate) (PET) flakes orig...

Europe - EFSA - European Food Safety Authority Publications

30-7-2018

ANSES recommends that certain populations avoid the consumption of food supplements containing melatonin

ANSES recommends that certain populations avoid the consumption of food supplements containing melatonin

Under the national nutrivigilance scheme, reports of adverse effects likely to be associated with the consumption of food supplements containing melatonin have been brought to the attention of ANSES. A retrospective analysis of these reports, combined with the considerable level of consumption of this type of supplement, led ANSES to conduct an assessment of the potential health risks. In its Opinion of February 2018, the Agency highlighted the existence of populations and situations at risk, for which t...

France - Agence Nationale du Médicament Vétérinaire

18-7-2018

MZ izdalo dovoljenje za opravljanje zdravstvene dejavnosti NIOSB

MZ izdalo dovoljenje za opravljanje zdravstvene dejavnosti NIOSB

Ministrstvo za zdravje je včeraj, 17. 7. 2018, izdalo dovoljenje za opravljanje zdravstvene...

Ministrstvo za zdravje

11-7-2018

Ministrica za zdravje na srečanju ministrov za zdravje držav članic Zdravstvene mreže JV Evrope in partnerskih držav ter partnerskih organizacij Zdravstvene mreže JV Evrope

Ministrica za zdravje na srečanju ministrov za zdravje držav članic Zdravstvene mreže JV Evrope in partnerskih držav ter partnerskih organizacij Zdravstvene mreže JV Evrope

Ministrica za zdravje se je kot vabljena predstavnica partnerske države Zdravstvene mreže...

Ministrstvo za zdravje

10-7-2018

Uvodni nagovor državne sekretarke dr. Ane Medved na izredni seji DZ  - novela Zakona o zdravniški službi

Uvodni nagovor državne sekretarke dr. Ane Medved na izredni seji DZ - novela Zakona o zdravniški službi

Spoštovane poslanke in poslanci, odhod vseh vrhunsko usposobljenih specialistov za ozko in zelo...

Ministrstvo za zdravje

28-6-2018

The Facts on Tampons—and How to Use Them Safely

The Facts on Tampons—and How to Use Them Safely

Tampons are medical devices regulated by the U.S. Food and Drug Administration. And if you or a loved one uses them, it's important to use them safely. Learn the basics and consider this advice.

FDA - U.S. Food and Drug Administration

14-6-2018

ANSES consolidates its presence in Boulogne-sur-Mer!

ANSES consolidates its presence in Boulogne-sur-Mer!

Centrally located in the port of Boulogne-sur-Mer, the Laboratory for Food Safety's site specialising in fishery and aquaculture products is expanding! This extension, financed jointly by the Hauts-de-France Region and the local community, underlines ANSES's scientific investment in Boulogne-sur-Mer and is fully consistent with regional research dynamics for the quality and safety of aquatic products.

France - Agence Nationale du Médicament Vétérinaire

25-5-2018

Urgent Medical Device Recall: Sam XT Extremity Tourniquet

Urgent Medical Device Recall: Sam XT Extremity Tourniquet

SAM Medical today announced it is conducting a voluntary international recall of all unused SAM XT Extremity Tourniquets (SAM XT). The company initiated the recall after internal testing indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human patient to stop arterial blood flow. To date, there have been no reports of adverse health consequences received. This recall is being made with the knowledge of the Food and Drug A...

FDA - U.S. Food and Drug Administration

23-5-2018

Ministrica za zdravje na srečanju s predsednikom Svetovne zdravstvene organizacije dr. Tedrosom Adhanomom Ghebreyesusom

Ministrica za zdravje na srečanju s predsednikom Svetovne zdravstvene organizacije dr. Tedrosom Adhanomom Ghebreyesusom

Ministrica za zdravje Milojka Kolar Celarc se je danes uradno srečala z generalnim direktorjem...

Ministrstvo za zdravje

21-5-2018

Ministrica za zdravje Milojka Kolar Celarc se je danes srečala z regionalno direktorico Svetovne zdravstvene organizacije

Ministrica za zdravje Milojka Kolar Celarc se je danes srečala z regionalno direktorico Svetovne zdravstvene organizacije

Ministrica za zdravje Milojka Kolar Celarc se je v okviru 71. zasedanja Generalne skupščine Svetovne...

Ministrstvo za zdravje

19-5-2018

Hickory Harvest Recalls Certain Island Fruit Mix and Organic Nut Mix Products Because of Possible Health Risk

Hickory Harvest Recalls Certain Island Fruit Mix and Organic Nut Mix Products Because of Possible Health Risk

Hickory Harvest Foods of Akron, Ohio is voluntarily recalling specific lots due to the potential exposure to Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, pregnant women, and others with weakened immune systems. Healthy individuals may experience short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea. Listeria infection can also cause miscarr...

FDA - U.S. Food and Drug Administration

15-5-2018

Nonprescription Drugs Advisory Committee

Nonprescription Drugs Advisory Committee

he Nonprescription Drugs Advisory Committee advises the Commissioner or designee in discharging responsibilities as they relate to helping to ensure safe and effective drugs for human use and, as required, any other product for which the Food and Drug Administration has regulatory responsibility.

FDA - U.S. Food and Drug Administration

9-5-2018

Medication Safety: Advice for New Parents

Medication Safety: Advice for New Parents

Mother's Day and Father's Day are exciting for new parents. But moms and dads of babies 12 months and younger can also have some worries. Medical officers at the U.S. Food and Drug Administration offer health suggestions.

FDA - U.S. Food and Drug Administration

8-5-2018

What to Know When Buying or Using a Breast Pump

What to Know When Buying or Using a Breast Pump

Breast pumps are medical devices regulated by the U.S. Food and Drug Administration. They can be used to extract milk, maintain or increase a woman's milk supply, and relieve engorged breasts (among other indications). But, to protect mothers and their babies, there are important safety considerations to know before using one.

FDA - U.S. Food and Drug Administration

17-4-2018

Ministrica za zdravje na otvoritvi sejma Medical v Gornji Radgoni

Ministrica za zdravje na otvoritvi sejma Medical v Gornji Radgoni

Ministrica za zdravje se je danes udeležila otvoritve sejma Medical v Gornji Radgoni V nagovoru je...

Ministrstvo za zdravje

9-4-2018

Na ministrstvu za zdravje predstavili nov način razpisovanja specializacij

Na ministrstvu za zdravje predstavili nov način razpisovanja specializacij

Spoštovani mladi zdravniki in predstavniki izvajalcev zdravstvene dejavnosti v mreži javne...

Ministrstvo za zdravje

6-4-2018

5 Things to Know About Breast Implants

5 Things to Know About Breast Implants

The U.S. Food and Drug Administration regulates breast implants as medical devices. Learn about the risks of these products, and consider this advice.

FDA - U.S. Food and Drug Administration

1-2-2018

Ministrica za zdravje bo predstavila predlog Zakona o zdravstvenem varstvu in zdravstvenem zavarovanju in predlog Zakona o dolgotrajni oskrbi

Ministrica za zdravje bo predstavila predlog Zakona o zdravstvenem varstvu in zdravstvenem zavarovanju in predlog Zakona o dolgotrajni oskrbi

KAJ: Ministrica za zdravje Milojka Kolar Celarc bo predstavila izhodišča in novosti ter ključnih...

Ministrstvo za zdravje

19-12-2017

Ministrica za zdravje podpisala sklep o razpisu specializacij

Ministrica za zdravje podpisala sklep o razpisu specializacij

Ministrica za zdravje Milojka Kolar Celarc je, na podlagi novele Zakona o zdravniški službi (ZdrS)...

Ministrstvo za zdravje

15-12-2017

Ministrica Milojka Kolar Celarc ob dnevu Zveze društev upokojencev Slovenije: "Temelj našega zdravstvenega sistema je javno zdravstvo"

Ministrica Milojka Kolar Celarc ob dnevu Zveze društev upokojencev Slovenije: "Temelj našega zdravstvenega sistema je javno zdravstvo"

Ministrica za zdravje Milojka Kolar Celarc se je, poleg obiska SB Izola, danes udeležila slavnostne...

Ministrstvo za zdravje

7-10-2014

New rules for persons collaborating with the industry

New rules for persons collaborating with the industry

As of 1 November 2014, new rules governing healthcare professionals' collaboration with pharmaceutical and medical companies take effect. The rules governing association will be extended to include medical companies and nurses. Doctors' association with speciality stores trading in medical devices are also covered by the rules.

Danish Medicines Agency

21-10-2018

Although I’ve been focusing on medical products, we're also advancing our food safety and nutrition work, such as our joint advice w/ EPA on making informed choices about eating fish for women who are pregnant, may become pregnant or are breastfeeding  ht

Although I’ve been focusing on medical products, we're also advancing our food safety and nutrition work, such as our joint advice w/ EPA on making informed choices about eating fish for women who are pregnant, may become pregnant or are breastfeeding ht

Although I’ve been focusing on medical products, we're also advancing our food safety and nutrition work, such as our joint advice w/ EPA on making informed choices about eating fish for women who are pregnant, may become pregnant or are breastfeeding https://go.usa.gov/xPnda . pic.twitter.com/nktV9BDAC3

FDA - U.S. Food and Drug Administration

22-8-2018

Routine eye exams and visiting your eye doctor will help ensure and maintain healthy eyes for everyone. #OnePairTakeCare #FDA #MedicalDevicepic.twitter.com/SQYFz30oFy

Routine eye exams and visiting your eye doctor will help ensure and maintain healthy eyes for everyone. #OnePairTakeCare #FDA #MedicalDevicepic.twitter.com/SQYFz30oFy

Routine eye exams and visiting your eye doctor will help ensure and maintain healthy eyes for everyone. #OnePairTakeCare #FDA #MedicalDevice pic.twitter.com/SQYFz30oFy

FDA - U.S. Food and Drug Administration

18-7-2018

HSCC announced today a new workstream, conducted under the Task Group, that will discuss and seek input on a software bill of materials (SBOM) for medical devices. SBOMs can ensure that users have better understanding of what software elements are in a me

HSCC announced today a new workstream, conducted under the Task Group, that will discuss and seek input on a software bill of materials (SBOM) for medical devices. SBOMs can ensure that users have better understanding of what software elements are in a me

HSCC announced today a new workstream, conducted under the Task Group, that will discuss and seek input on a software bill of materials (SBOM) for medical devices. SBOMs can ensure that users have better understanding of what software elements are in a medical device.

FDA - U.S. Food and Drug Administration

3-7-2018

The Pediatric Medical Device Development public meeting is August 13-14 at #FDA White Oak Campus. Do you know how the FDA defines “pediatrics” for medical device purposes? Click the link for the answer and more info on #Pediatric #MedicalDevices  https://

The Pediatric Medical Device Development public meeting is August 13-14 at #FDA White Oak Campus. Do you know how the FDA defines “pediatrics” for medical device purposes? Click the link for the answer and more info on #Pediatric #MedicalDevices https://

The Pediatric Medical Device Development public meeting is August 13-14 at #FDA White Oak Campus. Do you know how the FDA defines “pediatrics” for medical device purposes? Click the link for the answer and more info on #Pediatric #MedicalDevices https://go.usa.gov/xU2e8 

FDA - U.S. Food and Drug Administration

29-5-2018

Ensure that you have optimised your Class I medical device ARTG entries

Ensure that you have optimised your Class I medical device ARTG entries

Information sheet to assist sponsors to optimise their Class I ARTG

Therapeutic Goods Administration - Australia