Tunisie - français - Ministère de la Santé, Direction de l'inspection Pharmaceutique

h.lundbeck a/s - la mÉmantine - comprimé pelliculé - 10 mg - systeme nerveux - psychoanaleptiques - traitement des patients atteints d'une forme modérée à sévère de la maladie d'alzheimer.

Tunisie - français - Ministère de la Santé, Direction de l'inspection Pharmaceutique

h.lundbeck a/s - la mÉmantine - comprimé pelliculé - 20 mg - systeme nerveux - psychoanaleptiques - traitement des patients atteints d'une forme modérée à sévère de la maladie d'alzheimer.

Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

elixan aromatica gmbh - melaleucae aetheroleum - flüssigkeit zur herstellung eines dampfes zur inhalation / einer gurgellösung - melaleucae aetheroleum, à la solution pro 1.g. - lors de l'inflammation dans la bouche ou la gorge - phytoarzneimittel

Canada - français - Health Canada

merck canada inc - prp d'haemophilus influenzae de type b; complexe protéique de la membrane externe du neisseria meningitidis - suspension - 7.5mcg; 125mcg - prp d'haemophilus influenzae de type b 7.5mcg; complexe protéique de la membrane externe du neisseria meningitidis 125mcg - vaccines

Canada - français - Health Canada

glaxosmithkline inc - protéine nhba hybride recombinante de neisseria meningitidis du sérogroupe b; protéine nada recombinante de neisseria meningitidis du sérogroupe b; protéine fhbp hybride recombinante de neisseria meningitidis du sérogroupe b; vésicules de membrane externe (neisseria meningitidis group b souche nz98/254) - suspension - 50mcg; 50mcg; 50mcg; 25mcg - protéine nhba hybride recombinante de neisseria meningitidis du sérogroupe b 50mcg; protéine nada recombinante de neisseria meningitidis du sérogroupe b 50mcg; protéine fhbp hybride recombinante de neisseria meningitidis du sérogroupe b 50mcg; vésicules de membrane externe (neisseria meningitidis group b souche nz98/254) 25mcg - vaccines

Union européenne - français - EMA (European Medicines Agency)

ceva-phylaxia co. ltd. - live recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus (rfp-lt) and avian encephalomyelitis virus, strain calnek 1143 (ae) - immunologicals for aves, live viral vaccines, domestic fowl - poulet - for active immunisation of chickens of 8 to 13 weeks of age in order to reduce the skin lesions due to fowlpox, to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis and to prevent egg production losses due to avian encephalomyelitis.

Union européenne - français - EMA (European Medicines Agency)

ceva-phylaxia co. ltd. - recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus, live - poulet - for active immunisation of chickens from 8 weeks of age in order to reduce the skin lesions due to fowlpox and to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis.

Union européenne - français - EMA (European Medicines Agency)

novartis europharm limited  - gozetotide - imagerie des radionucléides - produits radiopharmaceutiques de diagnostic - ce médicament est destiné à un usage diagnostique uniquement. locametz, after radiolabelling with gallium 68, is indicated for the detection of prostate specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high risk pca prior to primary curative therapy,suspected pca recurrence in patients with increasing levels of serum prostate specific antigen (psa) after primary curative therapy,identification of patients with psma positive progressive metastatic castration resistant prostate cancer (mcrpc) for whom psma targeted therapy is indicated (see section 4.

Union européenne - français - EMA (European Medicines Agency)

novartis europharm limited  - lutetium (177lu) vipivotide tetraxetan - bénigne de la prostate tumeurs, résistant À la castration - produits radiopharmaceutiques thérapeutiques - pluvicto in combination with androgen deprivation therapy (adt) with or without androgen receptor (ar) pathway inhibition is indicated for the treatment of adult patients with progressive prostate-specific membrane antigen (psma)-positive metastatic castration-resistant prostate cancer (mcrpc) who have been treated with ar pathway inhibition and taxane based chemotherapy.

Union européenne - français - EMA (European Medicines Agency)

curium pet france - piflufolastat (18f) - néoplasmes prostatiques - produits radiopharmaceutiques de diagnostic - ce médicament est destiné à un usage diagnostique uniquement. pylclari is indicated for the detection of prostate-specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high-risk pca prior to initial curative therapy,to localize recurrence of pca in patients with a suspected recurrence based on increasing serum prostate-specific antigen (psa) levels after primary treatment with curative intent. pylclari is indicated for use with positron emission tomography (pet).