Vertaling van "included the once-yearly " (Nederlands → Frans) :

Top performers among recently launched medicines included the once-yearly osteoporosis therapy Aclasta/Reclast (USD 254 million), the age-related macular degeneration drug Lucentis (USD 886 million) and the addition of Exelon Patch, a skin patch formulation for Alzheimer’s disease that has reinvigorated the Exelon franchise (USD 815 million).
Parmi les médicaments récemment lancés ayant réalisé les meilleures performances se trouvent Aclasta/Reclast (USD 254 millions), traitement annuel contre l’ostéoporose, Lucentis (USD 886 millions), contre la cécité liée à l’âge, et l’addition d’Exelon Patch, un patch transdermique contre la maladie d’Alzheimer qui a revigoré le secteur d’activité Exelon (USD 815 millions).

Reclast/Aclasta (USD 142 million, +23% cc), the only once-yearly osteoporosis treatment available in over 90 countries, maintained a steady pace of growth.
Aclasta/Reclast (USD 142 millions, +23% tcc), le seul traitement contre l’ostéoporose administré par une perfusion unique par an, est disponible dans plus de 90 pays et progresse avec régularité.

Reclast/Aclasta (USD 143 million, +15% cc) is the only once-yearly osteoporosis therapy available in over 90 countries.
Aclasta/Reclast (USD 143 millions, +15% tcc) est l’unique traitement contre l’ostéoporose administré en perfusion une seule fois par an et disponible dans plus de 90 pays.

Reclast/Aclasta (USD 325 million, +100% lc), the first once-yearly infusion therapy for osteoporosis, continues to expand on increasing patient access to infusion centers and a broad range of use in patients suffering from various types of this debilitating disease.
Aclasta/Reclast (USD 325 millions, +100% en m. l.), le premier traitement de l’ostéoporose par perfusion annuelle, poursuit sa croissance en facilitant l’accès des malades aux centres de perfusion ainsi qu’en allongeant la liste des indications autorisées pour une utilisation chez les patients souffrant de différents types de cette maladie invalidante.

Reclast/Aclasta (USD 472 million, +88% lc), a once-yearly infusion therapy for osteoporosis, continues to expand on increasing patient access to infusion centers and a broad range of use in patients with various types of this debilitating bone disease.
Aclasta/Reclast (USD 472 millions, +88% en m. l.), traitement de l’ostéoporose par perfusion annuelle unique, poursuit sa croissance en facilitant l’accès des malades aux centres de perfusion ainsi qu’en allongeant la liste des indications autorisées pour de nombreuses utilisations chez les patients souffrant de différents types de cette maladie osseuse invalidante.

Reclast/Aclasta (USD 200 million, +105% lc), the first once-yearly infusion therapy for osteoporosis, has been fueled by increasing patient access to infusion centers in the US and Europe as well as a growing list of approved indications for use in a broad range of patients suffering from various types of this debilitating disease.
Aclasta/Reclast (USD 200 millions, +105% en m. l.), premier traitement de l’ostéoporose par perfusion annuelle, a bénéficié de l’accroissement du nombre de centres de perfusion facilitant l’accès aux malades aux Etats-Unis et en Europe ainsi que l’allongement de la liste des indications autorisées pour une utilisation chez de nombreux malades souffrant de différents types de cette maladie invalidante.

Once-yearly zoledronic acid for treatment of postmenopausal osteoporis.
Once-yearly zoledronic acid for treatment of postmenopausal osteoporosis.

Aclasta/Reclast (USD 254 million), the first once-yearly infusion therapy for various forms of osteoporosis, has now been used in more than 350,000 patients and has experienced consistent growth since its launch to treat postmenopausal osteoporosis in late 2007.
Aclasta/Reclast (USD 254 millions), première injection annuelle pour soigner différentes formes d’ostéoporose, a été utilisé par plus de 350 000 patients et a affiché une croissance notable depuis son lancement, à fin 2007, pour le traitement de l’ostéoporose potsménopausique.

The simplest, most efficient and safest treatment combines the application of a mupirocin nasal ointment (3 x/day in the anterior nostrils) and body wash (including skin lesions) with an antiseptic soap (chlorhexidine or polyvidone-iodine based) once a day for 5 days.
Le traitement le plus simple, le plus efficace et le plus sûr combine l'application d'un onguent nasal de mupirocine (3 x/jour dans les narines antérieures) et un lavage du corps (y compris les lésions cutanées) avec du savon antiseptique (à base de chlorhexidine ou d’iode polyvidone) une fois par jour pendant 5 jours.

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.