Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - ambrisentan - hypertension pulmonaire - antihypertenseurs, - volibris is indicated for treatment of pulmonary arterial hypertension (pah) in adult patients of who functional class (fc) ii to iii, including use in combination treatment (see section 5.  efficacy has been shown in idiopathic pah (ipah) and in pah associated with connective tissue disease. volibris is indicated for treatment of pah in adolescents and children (aged 8 to less than 18 years) of who functional class (fc) ii to iii including use in combination treatment. efficacy has been shown in ipah, familial, corrected congenital and in pah associated with connective tissue disease (see section 5.

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - niraparib (tosilate monohydrate) - fallopian tube neoplasms; peritoneal neoplasms; ovarian neoplasms - agents antinéoplasiques - zejula is indicated: , as monotherapy for the maintenance treatment of adult patients with advanced epithelial (figo stages iii and iv) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. , as monotherapy for the maintenance treatment of adult patients with platinum sensitive relapsed high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy.

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline biologicals sa - recombinant varicella zoster virus glycoprotein e - l'herpès zoster - vaccins - shingrix is indicated for prevention of herpes zoster (hz) and post-herpetic neuralgia (phn), in:adults 50 years of age or older;adults 18 years of age or older at increased risk of hz. l'utilisation de shingrix doit être en conformité avec les recommandations officielles.

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline trading services limited - le zanamivir - grippe humaine - antiviraux à usage systémique - dectova est indiqué pour le traitement de complexes et potentiellement la vie en danger de la grippe a ou b, le virus de l'infection chez les adultes et les patients pédiatriques (âgés de ≥6 mois) quand:le patient du virus de la grippe est connu ou suspecté de l'être résistante aux anti-grippe médicaments autres que le zanamivir, et/orother anti-virale médicaments pour le traitement de la grippe, y compris le zanamivir inhalé, ne sont pas appropriés pour le patient individuel. dectova doit être utilisé selon les recommandations officielles.

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - belantamab mafodotin - le myélome multiple - agents antinéoplasiques - blenrep is indicated as monotherapy for the treatment of multiple myeloma in adult patients, who have received at least four prior therapies and whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - dostarlimab - endometrial neoplasms - antineoplastic agents and antibody drug conjugates - jemparli is indicated as monotherapy for the treatment of adult patients with mismatch repair deficient (dmmr)/microsatellite instability-high (msi h) recurrent or advanced endometrial cancer (ec) that has progressed on or following prior treatment with a platinum-containing regimen.

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline trading services limited - sotrovimab - covid-19 virus infection - des sérums et immunoglobulines, - xevudy is indicated for the treatment of adults and adolescents (aged 12 years and over and weighing at least 40 kg) with coronavirus disease 2019 (covid-19) who do not require oxygen supplementation and who are at increased risk of progressing to severe covid-19.

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - le bromure d'umeclidinium, vilanterol trifenatate - maladie pulmonaire, chronique obstructive - les médicaments pour les maladies respiratoires obstructives, - anoro ellipta est indiqué comme traitement bronchodilatateur d'entretien pour soulager les symptômes chez les patients adultes atteints de maladie pulmonaire obstructive chronique (mpoc).

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - bromure d'uméclidinium - maladie pulmonaire, chronique obstructive - les médicaments pour les maladies respiratoires obstructives, - indiqué comme un traitement bronchodilatateur d'entretien pour soulager les symptômes chez les patients adultes atteints de bronchopneumopathie chronique obstructive (bpco).

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline trading services - furoate de fluticasone, bromure d'uméclidinium, trifénatate de vilantérol - maladie pulmonaire, chronique obstructive - les médicaments pour les maladies respiratoires obstructives, - trelegy ellipta est indiqué comme un traitement d’entretien chez l’adulte avec modéré à grave maladie pulmonaire obstructive chronique (mpoc) qui ne sont pas traités de façon adéquate par une combinaison d’un corticostéroïde en inhalation et un agoniste β2 longue durée d’action.