Traduction de «adverse effects and adverse events attributable » (Néerlandais → Français) :

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.

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

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)

Voor elk adverse event werd de verantwoordelijkheid van het gezondheidszorgmanagement en de vermijdbaarheid van het adverse event geëvalueerd op een schaal van 1 (geen) tot 6 (volledig) door een van de teams.
Pour chacun des événements indésirables, le degré de responsabilité imputable à la gestion des soins et d’évitabilité de l'événement indésirable ont été notés sur une échelle de 1 (absence de responsabilité et de possibilité de prévention) à 6 (pleine responsabilité et possibilité de prévention) par l'une des équipes.

Op internationaal vlak wordt de prevalentie van adverse events in acute ziekenhuizen tussen 2,9% en 16,6% geschat, afhankelijk van het type adverse event.
La prévalence internationale des événements indésirables dans les hôpitaux aigus a été évaluée comme étant comprise entre 2.9 % et 16.6 %, en fonction de type d’événement indésirable.

Ter verduidelijking: verschil en verband tussen ziekenhuisinfecties, ‘adverse events’ en medische fouten Het KCE stelde vast dat de media vaak de begrippen ziekenhuisinfecties, medische fouten en ongewenste complicaties (of ‘adverse events’) door elkaar gebruiken.
Une mise au point au sujet des différences et des liens entre évènement indésirable (adverse event), infection nosocomiale et erreur médicale Le KCE a constaté que dans les médias, ces trois concepts sont parfois confondus.

Uit een eerdere KCE studie blijkt dat het opsporen van adverse events via administratieve databanken kan verbeterd worden door een aangepaste registratie van de opnamegegevens. Ziekenhuisinfecties, ook nosocomiale infecties genoemd, behoren dus ook tot de adverse events.
Les infections nosocomiales sont un des événements indésirables possibles.

serious adverse events associated with the collection, testing, processing, storage and distribution of blood or blood components that may have an effect on their quality or safety ●● Collecting and evaluating information about
serious adverse events associated with the collection, testing, processing, storage and distribution of blood or blood components that may have an effect on their quality or safety ●● Collecting and evaluating information about

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

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