Vertaling van "reporting adverse effects and adverse " (Nederlands → Frans) :

Table 3: Update of evidence found in SR and HTA Search Radiation harms of mammography screening (40-49 y) questions Note Update of HTA (ETMIS) Date 03/05/2010 Keywords Breast neoplasms, mammography/ adverse effects, mass screening/ adverse effects Medline Case report.tw (156081) (OVID): 2 Letter.pt (689184) Filter 3 Historical article.pt (263481) RCT 4 Review of reported cases.pt (0) 5 Review,multicase.pt (0) 6 or/1-5 (1099551) 7 Breast/ or Breast Diseases/ (30731) 8 Neoplasms/ (216844) 9 7 and 8 (536) 10 exp Breast Neoplasms/ (171800) 11 (breast$ adj5 neoplas$).tw (2557) 12 (breast$ adj5 cancer$).tw (135752) 13 (breast$ adj5 carcin$).tw (31777) 14 (breast$ adj5 tumo$).tw (23441) 15 (breast$ adj5 metasta$).tw (16582) 16 (breast$ adj5 malig$).tw (7361) 17 exp Carcinoma, Ductal, Breast/ (8472) 18 9 or 10 or 11 or 12 or 13 or 14 or 15 or 16 or 17 (207367) 19 Mammography/ae [Adverse Effects] (517) 20 Mass Screening/ae [Adverse Effects] (325) 21 19 or 20 (763) 22 18 and 21 (443) 23 22 not 6 (379) 24 limit 23 to (yr=" 2005 -Current" and " all adult (19 plus years)" and (dutch or english or french)) (44) 25 from 24 keep 1-44 (44)
Table 5: Update of evidence found in SR and HTA Search Radiation harms of mammography screening (40-49 y) questions Note Update of HTA (ETMIS) Date 03/05/2010 Keywords Breast neoplasms, mammography/ adverse effects, mass screening/ adverse effects Medline Case report.tw (156081) (OVID): 2 Letter.pt (689184) Filter 3 Historical article.pt (263481) RCT 4 Review of reported cases.pt (0) 5 Review,multicase.pt (0) 6 or/1-5 (1099551) 7 Breast/ or Breast Diseases/ (30731) 8 Neoplasms/ (216844) 9 7 and 8 (536) 10 exp Breast Neoplasms/ (171800) 11 (breast$ adj5 neoplas$).tw (2557) 12 (breast$ adj5 cancer$).tw (135752) 13 (breast$ adj5 carcin$).tw (31777) 14 (breast$ adj5 tumo$).tw (23441) 15 (breast$ adj5 metasta$).tw (16582) 16 (breast$ adj5 malig$).tw (7361) 17 exp Carcinoma, Ductal, Breast/ (8472) 18 9 or 10 or 11 or 12 or 13 or 14 or 15 or 16 or 17 (207367) 19 Mammography/ae [Adverse Effects] (517) 20 Mass Screening/ae [Adverse Effects] (325) 21 19 or 20 (763) 22 18 and 21 (443) 23 22 not 6 (379) 24 limit 23 to (yr=" 2005 -Current" and " all adult (19 plus years)" and (dutch or english or french)) (44) 25 from 24 keep 1-44 (44)

The evaluation of oncological adverse effects (as well as the evaluation of the Periodic Safety Update Report – PSUR, Annual Safety Report - ASR, Suspected Unexpected Serious Adverse Reaction
The evaluation of oncological adverse effects (as well as the evaluation of the Periodic Safety Update Report – PSUR, Annual Safety Report - ASR, Suspected Unexpected Serious Adverse Reaction

Healthcare professionals and consumers of medicines and health products need to be made aware of the utility and obligation (in the case of materiovigilance and haemovigilance) of reporting adverse effects and adverse events associated with the use of medicines and health products to the FAMHP. Furthermore, the report form should be made easy to complete
Healthcare professionals and consumers of medicines and health products need to be made aware of the utility and obligation (in the case of materiovigilance and haemovigilance) of reporting adverse effects and adverse events associated with the use of medicines and health products to the FAMHP. Furthermore, the report form should be made easy to complete

Both the SCF’s 2003 opinion and the advisory report recently published by the German Federal Institute for Risk Assessment (BfR, 2008) mention a number of observation cases and reported cases with acute adverse effects, including death, in people who consume energy drinks.
L’avis du SCF de 2003 ainsi que l’avis récemment émis par l’Institut fédéral allemand d’évaluation des risques (BfR, 2008) mentionnent un certain nombre de cas d’observation et de cas rapportés signalant des effets nocifs aigus, comprenant des décès, chez des sujets consommant des boissons énergisantes.

Each report of an adverse effect is now processed in two phases. For the first phase “preparing” the electronic report approximately 60 % of the backlog has been removed.
Each report of an adverse effect is now processed in two phases. For the first phase “preparing” the electronic report approximately 60 % of the backlog has been removed.

AAA aromatic amino acids aromatische aminozuren ADH aanbevolen dagelijkse hoeveelheid AR average requirement gemiddelde behoefte ATP adenosinetrifosfaat BMI body mass index BMR basal metabolic rate basaal metabolisme CLA conjugated linoleic acid geconjugeerd linolzuur DHA docosahexaëenzuur ΔE energievoorraad EAZ essentieel aminozuur EI energie-inname EPA eicosapentaëenzuur EV energieverbruik FAD flavineadenine-dinucleotide FMN flavine-mononucleotide GTF glucose tolerance factor glucose tolerantie factor His histidine IE internationale eenheid IEI integrated energy index geïntegreerde energie-index Ile isoleucine LA linolzuur LDL low density lipoprotein lage dichtheid lipoproteïne Leu leucine lg lichaamsgewicht LNA alfa-linoleenzuur LOAEL lowest observed adverse effect level LTI lowest treshold intake laagste opname-drempel Lys lysine MAO monoamineoxydase MUFA mono unsaturated fatty acids enkelvoudig onverzadigde vetzuren NHANES III third national health and nutrition examination survey NOAEL no observed adverse effect level NPU net protein utilisation netto eiwit benutting NSP non starch polysaccharides niet-zetmeel polymere koolhydraten
AAA aromatic amino acids acides aminés aromatiques AAE / AAI acide aminé essentiel / indispensable ADMR average daily metabolic rate AE apport énergétique AET apport énergétique total AJR apport journalier recommandé AR average requirement besoin moyen ATP adénosine triphosphate BMI body mass index BMR basal metabolic rate métabolisme basal (ou de base) CLA conjugated linoleic acid acide linoléique conjugué DE dépense énergétique DHA acide docosahexaénoïque ΔE réserve énergétique EPA acide eicosapentaénoïque ER équivalent rétinol ES énergie stockée FAD flavine adénine dinucléotide FMN flavine mononucléotide GTF glucose tolerance factor facteur de tolérace au glucose His histidine IEI integrated energy index indice énergétique intégré Ile isoleucine IQ Quetelet index indice de Quetelet (ou BMI) LDL low density lipoprotein lipoprotéine à faible densité Leu leucine LOAEL lowest observed adverse effect level LTI lowest treshold intake seuil d’apport le plus bas LA acide linoléique LNA acide linolénique Lys lysine MAO monoamine-oxydase MUFA mono unsaturated fatty acids acides gras monoinsaturés NHANES III third national health and nutrition examination survey NOAEL no observed adverse effect level NPU net protein utilisation utilisation protéique nette NSP non starch polysaccharides polysaccharides non amylacés PAI physical activity index PAL physical activity level niveau d’activité physique PAR physical activity ratio ratio d’activité physique p.c. poids corporel PDCAAS protein digestibility-corrected amino acid score

Lijst van de gebruikte afkortingen EFSA: European Food Safety Authority EU : Europese Unie FOD : Federale Overheidsdienst FSA : British Food Standards Agency HGR : Hoge Gezondheidsraad LOAEL : Lowest Adverse Effect Level NOAEL: No Observed Adverse Effect Level OIVO : Onderzoeks- en Informatiecentrum van de Verbruikersorganisaties RPE : Ratings of Perceived Exertion SCF : Scientific Committee on Food UL : tolerable Upper intake Level WIV : Wetenschappelijk Instituut Volksgezondheid
Liste des abréviations CRIOC : Centre de Recherche et d'Information des Organisations de Consommateurs CSS : Conseil Supérieur de la Santé EFSA: European Food Safety Authority FSA : British Food Standards Agency ISP : Institut Scientifique de Santé Publique LOAEL : Lowest Adverse Effect Level NOAEL: No Observed Adverse Effect Level RPE : Ratings of Perceived Exertion SCF : Scientific Committee on Food SPF : Service public fédéral UE : Union Européenne UL : tolerable Upper intake Level

At the end of 2007 the FAMHP initiated a programme for specific monitoring of new medicines (“black triangle” – symbol included in the BCFI-CBIP annotated drugs formulary – Gecommentarieerd Geneesmiddelenrepertorium – Répertoire Commenté des Médicaments) with the aim of encouraging healthcare professionals to report adverse effects of medicines with a new active substance to the FAMHP.
At the end of 2007 the FAMHP initiated a programme for specific monitoring of new medicines (“black triangle” – symbol included in the BCFI-CBIP annotated drugs formulary – Gecommentarieerd Geneesmiddelenrepertorium – Répertoire Commenté des Médicaments) with the aim of encouraging healthcare professionals to report adverse effects of medicines with a new active substance to the FAMHP.

A final element that needs to be added to this file is the very recent report of the French toxicovigilance co-ordination committee (Comité de Coordination de Toxicovigilance Français – CCTF) (CCTF, 2009). It describes the results of the prospective follow-up of the adverse effects of consuming energy drinks, especially during the five months that passed after the most famous of these drinks was allowed to be marketed in France (15 July 2008).
Un dernier élément à verser au dossier est le très récent rapport du comité de coordination de toxicovigilance français (CCTF) qui relate les résultats du suivi prospectif des effets indésirables liés à la consommation de boissons énergisantes, en particulier dans les 5 mois qui ont suivi l’autorisation de commercialisation de la plus connue d’entreelles en France (15 juillet 2008) (CCTF, 2009).

The prevention of adverse effects and adverse events attributable to the use of medicines and health products is closely linked with information for healthcare professionals and the public regarding the risks associated with the use of medicines and health products.
The prevention of adverse effects and adverse events attributable to the use of medicines and health products is closely linked with information for healthcare professionals and the public regarding the risks associated with the use of medicines and health products.