Traduction de «other potential » (Néerlandais → Français) :

TERMINOLOGIE

afwijkend(e) | elektro-oculogram [EOG] | afwijkend(e) | elektromyogram [EMG] | afwijkend(e) | elektroretinogram [ERG] | afwijkend(e) | respons op zenuwstimulatie | afwijkend(e) | visually evoked potential [VEP]
Anomalies (de):électromyogramme [EMG] | électro-oculogramme [EOG] | électrorétinogramme [ERG] | potentiels évoqués visuellement | réponse à une stimulation nerveuse

potentiëring | versterking
potentiation/potentialisation | augmentation de l'action d'un médicament par l'absorption d'un second

potentie | kracht
1) puissance sexuelle - 2) efficacité | 1) puissance sexuelle - 2) d'un médicament

TRADUCTIONS EN CONTEXTE

This release contains forward-looking information about an agreement by Pfizer to acquire FoldRx, and about FoldRx’s product candidate tafamidis, its other clinical and preclinical development programs and its technology platform, including their potential benefits, that involves substantial risks and uncertainties. Such risks and uncertainties include, among other things, the satisfaction of conditions to closing the agreement; the uncertainties inherent in research and development; whether and when a new drug application for tafamidis will be filed with the FDA; decisions by regulatory authorities regarding whether and when to approve any drug applications that have been or may be filed for tafamidis and that may be filed for any other product candidates that may be generated by FoldRx’s technology platform as well as their decisions regarding labeling and other matters that could affect the availability or commercial potential of tafamidis and such other product candidates; and competitive developments. A further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2009 and in its reports on Form 10-Q and Form 8-K.
Such risks and uncertainties include, among other things, the satisfaction of conditions to closing the agreement; the uncertainties inherent in research and development; whether and when a new drug application for tafamidis will be filed with the FDA; decisions by regulatory authorities regarding whether and when to approve any drug applications that have been or may be filed for tafamidis and that may be filed for any other product candidates that may be generated by FoldRx’s technology platform as well as their decisions regarding labeling and other matters that could affect the availability or commercial potential of tafamidis and such other product candidates; and competitive developments.

However, the Council remains concerned that these energy drinks increase the risk of excessive and potentially harmful caffeine consumption and its consequences (such as insomnia, nervousness, anxiety, headaches, trembling and tachycardia), as well as the risk of potentially inducing an addiction to caffeine and, as has been noted more recently, a dependence on other substances (nicotine, alcohol and/or cannabis).
Il reste néanmoins préoccupé par le risque accru d’une surconsommation potentiellement nuisible de caféine et des conséquences que celle-ci implique telles que insomnie, nervosité, anxiété, maux de tête, tremblements et tachycardie, mais également, la possibilité d’induction d’une dépendance à la caféine ou à d’autres substances (nicotine, alcool et/ou cannabis), plus récemment évoquée.

Such risks and uncertainties include, among other things, the uncertainties inherent in research and development; whether and when regulatory authorities in countries where regulatory applications for Prevenar 13 may be pending or may be submitted will approve such applications and their decisions regarding labeling and other matters that could affect its availability or commercial potential; and competitive developments.
This release contains forward-looking information that involves substantial risks and uncertainties regarding Prevenar 13, including its potential benefits; and the success of the AMC project for vaccines. Such risks and uncertainties include, among other things, the uncertainties inherent in research and development; whether and when regulatory authorities in countries where regulatory applications for Prevenar 13 may be pending or may be submitted will approve such applications and their decisions regarding labeling and other matters that could affect its availability or commercial potential; and competitive developments. A further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2009, and in its reports on Form 10-Q and Form 8-K.

This release contains forward-looking information about a potential joint venture between Pfizer and Zhejiang Hisun Pharmaceuticals (Hisun) including, among other things, the anticipated benefits there of, that involves substantial risks and uncertainties.
This information contained in this release is as of June 2, 2011, Pfizer assumes no obligation to update forward-looking statements contaiTned in this release as the result of new information or future events or developments. This release contains forward-looking information about a potential joint venture between Pfizer and Zhejiang Hisun Pharmaceuticals (Hisun) including, among other things, the anticipated benefits there of, that involves substantial risks and uncertainties.

The primary concern of doctors, pharmacists, and other health professionals is informing their patients and drawing their attention to the fact that it is of crucial importance to use the correct dosage (e.g. by drawing their attention to the potential side effects of a treatment once it has been started and explaining to them that antidepressants need a few weeks to take effect).
La plus grande préoccupation des médecins, pharmaciens et autres prestataires de soins de santé est d’informer les patients sur l’importance d’une posologie correcte et de les informer (par exemple en attirant l’attention sur des possibles effets secondaires d’un traitement entamé et en expliquant que les antidépresseurs ne commencent à être effectifs qu’au bout de quelques semaines).

Novartis is also cooperating with an inquiry by the EDPA regarding similar allegations of potential off-label marketing and promotion and payments to healthcare providers in connection with five other products: Diovan, Exforge, Sandostatin, Tekturna and Zelnorm.
Novartis coopère également avec l’EPDA dans le cadre d’une enquête concernant des accusations similaires en relation avec cinq autres produits: Diovan, Exforge, Sandostatine, Tekturna et Zelnorm.

Studies are underway to review potential anti-cancer benefits in other tumor types.
Des études sont en cours afin de déterminer les bénéfices anticancer potentiels de ce médicament dans d’autres types de tumeurs.

The SOE-USE will also be involved in control policy, and the current demarcation with other inspection units may potentially change.
The SOE-USE will also be involved in control policy, and the current demarcation with other inspection units may potentially change.

concerned about the increased risk of potentially harmful caffeine-abuse and all its consequences (such as insomnia, nervousness, anxiety, headache, trembling and tachycardia), as well as the fact that these beverages may induce an addiction to caffeine or, as has been discovered more recently, a dependence on other substances (nicotine, alcohol and/or cannabis).
En conséquence, le Conseil Supérieur de la Santé prend acte de la mise à disposition de données rassurantes sur l’innocuité de deux principaux composants des boissons énergisantes, à savoir la taurine et la D-glucuronolactone, mais reste préoccupé par le risque accru qu’elles entraînent d’une surconsommation potentiellement nuisible de caféine, avec les conséquences que celle-ci implique telles que insomnie, nervosité, anxiété, maux de tête, tremblements et tachycardie, mais également, la possibilité d’induction d’une dépendance à la caféine ou à d’autres substances (nicotine, alcool et/ou cannabis), plus récemment évoquée.