Traduction de «after treatment » (Néerlandais → Français) :

Spontaneous cessation rate: 2.5% OR counselling only: 1.73 Incremental OR NRT gum (relative to counselling only): 1.63 Incremental OR NRT patch (relative to counselling only): 1.79 Incremental OR NRT spray (relative to counselling only): 2.35 Incremental OR NRT inhaler (relative to counselling only): 2.14 Incremental OR bupropion (relative to counselling only): 2.30 % of smokers still under treatment after the first month: 50% (range 40-60% in sensitivity analysis) % of smokers still under treatment after the second month: 20% (range 15-25% in sensitivity analysis) Lifetime relapse probability after one year of abstinence: 35% (range 10-50% in sensitivity analysis) Effect of smoking cessation on mortality derived from the results of the American Cancer Society Prevention Study II. The mortality rate for former smokers was projected by calculating a weighted average of the incremental differentials between mortality rates of neversmokers and smokers, weighted according to the duration of abstinence.
Spontaneous cessation rate: 2.5% OR counselling only: 1.73 Incremental OR NRT gum (relative to counselling only): 1.63 Incremental OR NRT patch (relative to counselling only): 1.79 Incremental OR NRT spray (relative to counselling only): 2.35 Incremental OR NRT inhaler (relative to counselling only): 2.14 Incremental OR Buproprion (relative to counselling only): 2.30 % of smokers still under treatment after the first month: 50% (range 40-60% in sensitivity analysis) % of smokers still under treatment after the second month: 20% (range 15-25% in sensitivity analysis) Lifetime relapse probability after one year of abstinence: 35% (range 10-50% in sensitivity analysis) Effect of smoking cessation on mortality derived from the results of the American Cancer Society Prevention Study II. The mortality rate for former smokers was projected by calculating a weighted average of the incremental differentials between mortality rates of neversmokers and smokers, weighted according to the duration of abstinence.

Afinitor (USD 12 million), an oral inhibitor of the mTOR pathway, was launched in the US after regulatory approval was granted in March as the first therapy for patients with advanced renal cell carcinoma (kidney cancer) after failure of treatment with sunitinib or sorafenib.
Afinitor (USD 12 millions), inhibiteur par voie orale de la voie mTOR, a été lancé aux Etats-Unis après avoir reçu, en mars, son homologation en tant que traitement du carcinome avancé des cellules rénales (cancer du rein) après échec d’un traitement par sunitinib ou sorafenib.

Boutitie F, Pinede L, Schulman S et al. Influence of preceding length of anticoagulant treatment and initial presentation of venous thromboembolism on risk of recurrence after stopping treatment: analysis of individual participant’s data from seven trials.
Oudega R, Van Weert H, Stoffers H et al. NHG-Standaard: Diepe veneuze trombose.

In August, “The New England Journal of Medicine” published results from the landmark BIG 1-98 study affirming the five-year upfront use of Femara after surgery was an optimal treatment approach versus tamoxifen for postmenopausal women with early-stage, hormone-receptor positive breast cancer.
En août, «The New England Journal of Medicine» a publié les résultats de l’étude pivot BIG 1-98 qui démontrent que l’utilisation de Femara pendant cinq ans après l'intervention chirurgicale constituait une approche optimale par rapport au tamoxifène chez les femmes ménopausées atteintes d’un cancer du sein hormonodépendant précoce.

The optimal scenario for informing the patient with regard to decisions related to reimbursement of products linked to a specific treatment is similar to the previous one but (Figure 8) presents a higher number of respondents choosing “inside the organs” and “at each step”. Only 26% would choose to inform the patient outside the existing organs, and with a stronger preference on informing after the decision is taken.
The optimal scenario for informing the patient with regard to decisions related to reimbursement of products linked to a specific treatment is similar to the previous one but ( Figure 8) presents a higher number of respondents choosing “inside the organs” and “at each step”.

Afinitor (USD 38 million), an oral inhibitor of the mTOR pathway, received European approval in August 2009 for use in patients with advanced renal cell carcinoma (RCC, kidney cancer) whose disease progressed on or after treatment with VEGF-targeted therapy.
Afinitor (USD 38 millions), inhibiteur par voie orale de la voie mTOR, a obtenu son autorisation dans l’Union européenne en tant que traitement du carcinome avancé des cellules rénales (cancer du rein) chez les malades où le carcinome a progressé pendant ou après un traitement ciblé sur le VEGF.

Zelnorm Novartis subsidiaries are defendants in approximately 140 cases brought in US and Canadian courts in which plaintiffs claim to have experienced cardiovascular injuries after having been treated with Zelnorm, a treatment for irritable bowel syndrome and chronic constipation.
Zelnorm Des filiales de Novartis sont aujourd’hui défenderesses dans quelque 140 actions en justice intentées devant des tribunaux américains et canadiens. Les plaignants affirment avoir subi des lésions cardiovasculaires après avoir été traités avec Zelnorm, un traitement du côlon irritable et de la constipation chronique.

Afinitor, an oral inhibitor of the mTOR pathway, was launched in the US, Europe, Switzerland and Japan after first regulatory approvals in 2009 as a new treatment for advanced renal cell carcinoma (RCC, kidney cancer) following VEGF-targeted therapy.
Cet inhibiteur de la voie mTOR par administration orale, a été lancé aux Etats-Unis, en Europe, en Suisse et au Japon après avoir été homologué pour la première fois en 2009 comme nouveau traitement du carcinome avancé des cellules rénales (cancer du rein) à la suite d’un traitement ciblé sur le VGEF.

Zometa/Aredia product liability litigation NPC is a defendant in approximately 680 cases brought in US courts in which plaintiffs claim to have experienced osteonecrosis of the jaw after treatment with Zometa or Aredia, which are used to treat patients whose cancer has spread to the bones.
Zometa/Aredia : litige ayant trait à la responsabilité produit Novartis Pharmaceuticals Corp. est défenderesse dans quelque 680 actions en justice intentées devant des tribunaux américains par des demandeurs qui affirment avoir développé une ostéonécrose de la mâchoire après avoir été traités par Zometa ou Aredia, qui sont utilisés dans les métastases osseuses du cancer.

Zometa/Aredia product liability litigation NPC is a defendant in approximately 690 cases brought in US courts in which plaintiffs claim to have experienced osteonecrosis of the jaw after treatment with Zometa or Aredia, which are used to treat patients whose cancer has spread to the bones.
Zometa/Aredia : litige ayant trait à la responsabilité produit NPC est défenderesse dans quelque 690 actions en justice intentées devant des tribunaux américains par des demandeurs qui affirment avoir développé une ostéonécrose de la mâchoire après avoir été traités par Zometa ou Aredia, qui sont utilisés dans les métastases osseuses du cancer.