AMOREPACIFIC FUTURE RESPONSE AGE DEFENSE CRÈME SPF 30 Crème Կանադա - ֆրանսերեն - Health Canada

amorepacific future response age defense crème spf 30 crème

amorepacific corporation - dioxyde de titane; octinoxate; octisalate; octocrilène - crème - 4.4%; 7%; 4.5%; 8% - dioxyde de titane 4.4%; octinoxate 7%; octisalate 4.5%; octocrilène 8% - sunscreen agents

AMOREPACIFIC FUTURE RESPONSE AGE DEFENSE DUAL EYE CRÈME WITH SPF 25 SUNSCREEN Crème Կանադա - ֆրանսերեն - Health Canada

amorepacific future response age defense dual eye crème with spf 25 sunscreen crème

amorepacific corporation - dioxyde de titane; octinoxate; octisalate; octocrilène - crème - 4.4%; 7%; 4.5%; 8% - dioxyde de titane 4.4%; octinoxate 7%; octisalate 4.5%; octocrilène 8% - sunscreen agents

Yesafili Եվրոպական Միություն - ֆրանսերեն - EMA (European Medicines Agency)

yesafili

viatris limited - aflibercept - macular edema; retinal vein occlusion; diabetic retinopathy; myopia, degenerative; diabetes complications - ophtalmologiques - yesafili is indicated for adults for the treatment ofneovascular (wet) age-related macular degeneration (amd) (see section 5. 1),visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo) (see section 5. 1),visual impairment due to diabetic macular oedema (dme) (see section 5. 1),visual impairment due to myopic choroidal neovascularisation (myopic cnv) (see section 5.

Luminity Եվրոպական Միություն - ֆրանսերեն - EMA (European Medicines Agency)

luminity

lantheus eu limited - perflutren - echocardiographie - contraste - ce médicament est destiné à un usage diagnostique uniquement. luminity est une échographie améliorant le contraste de l'agent pour l'utilisation dans les patients dans qui la non-échocardiographie de contraste a été sous-optimale (sous-optimale est considéré comme l'indiquent qu'au moins deux des six segments de l'ordre de 4 ou de 2 chambre vue sur le ventricule frontière n'étaient pas évaluables) et qui ont présumée ou établie la maladie coronarienne, de fournir l'opacification des cavités cardiaques et de l'amélioration du ventricule gauche endocardique délimitation de la frontière à la fois le repos et le stress.

Naglazyme Եվրոպական Միություն - ֆրանսերեն - EMA (European Medicines Agency)

naglazyme

biomarin international limited - la galsulfase - mucopolysaccharidose vi - d'autres tractus digestif et le métabolisme des produits, - naglazyme est indiqué pour la thérapie de remplacement d’enzymes à long terme chez les patients ayant un diagnostic confirmé de mucopolysaccharidose de type vi (mps vi ; n-acétylgalactosamine-4-sulfatase déficit ; maroteaux-lamy syndrome) (voir la section 5. comme pour tous les lysosomale troubles génétiques, il est de toute première importance, en particulier dans les formes sévères, pour initier le traitement le plus tôt possible, avant l'apparition de non-réversible manifestations cliniques de la maladie. une question clé est de traiter les patients âgés de.

Revolade Եվրոպական Միություն - ֆրանսերեն - EMA (European Medicines Agency)

revolade

novartis europharm limited - eltrombopag - purpura, thrombocytopénique, idiopathique - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 et 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 et 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

Enerzair Breezhaler Եվրոպական Միություն - ֆրանսերեն - EMA (European Medicines Agency)

enerzair breezhaler

novartis europharm limited - indacaterol, glycopyrronium bromide, mometasone - asthme - les médicaments pour les maladies respiratoires obstructives, - enerzair breezhaler is indicated as a maintenance treatment of asthma in adult patients not adequately controlled with a maintenance combination of a long acting beta2 agonist and a high dose of an inhaled corticosteroid who experienced one or more asthma exacerbations in the previous year.

Bemrist Breezhaler Եվրոպական Միություն - ֆրանսերեն - EMA (European Medicines Agency)

bemrist breezhaler

novartis europharm limited  - indacaterol, mometasone furoate - asthme - les médicaments pour les maladies respiratoires obstructives, - bemrist breezhaler is indicated as a maintenance   treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Zimbus Breezhaler Եվրոպական Միություն - ֆրանսերեն - EMA (European Medicines Agency)

zimbus breezhaler

novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - asthme - les médicaments pour les maladies respiratoires obstructives, - maintenance treatment of asthma in adults whose disease is not adequately controlled.