Rivastigmine Actavis Unjoni Ewropea - Malti - EMA (European Medicines Agency)

rivastigmine actavis

actavis group ptc ehf - rivastigmine hydrogen tartrate - dementia; alzheimer disease; parkinson disease - psychoanaleptics, - trattament sintomatiku ta 'dimenzja ta' alzheimer ħafifa għal moderatament gravi. kura sintomatika ta 'minn ħafifa għal moderatament gravi dimenzja f'pazjenti bil-marda idjopatika ta' parkinson.

Tadalafil Mylan Unjoni Ewropea - Malti - EMA (European Medicines Agency)

tadalafil mylan

mylan pharmaceuticals limited - tadalafil - disfunzjoni erettili - uroloġiċi - trattament ta 'disfunzjoni erettili f'annimali adulti. sabiex tadalafil ikun effettiv, l-istimulazzjoni sesswali hija meħtieġa. tadalafil mylan mhuwiex indikat għall-użu min-nisa.

Zinforo Unjoni Ewropea - Malti - EMA (European Medicines Agency)

zinforo

pfizer ireland pharmaceuticals - ceftaroline fosamil - community-acquired infections; skin diseases, infectious; pneumonia - antibatteriċi għal użu sistemiku, - zinforo is indicated for the treatment of the following infections in neonates, infants, children, adolescents and adults: , complicated skin and soft tissue infections (cssti), community-acquired pneumonia (cap) , consideration should be given to official guidance on the appropriate use of antibacterial agents.

Nerlynx Unjoni Ewropea - Malti - EMA (European Medicines Agency)

nerlynx

pierre fabre medicament - neratinib - neoplażmi tas-sider - aġenti antineoplastiċi - nerlynx huwa indikat għall-estiż kura awżiljarja ta 'pazjenti adulti bil-istadju bikri pożittiv għar-riċetturi tal-ormon tat-her2-overexpressed/amplifikati-kanċer tas-sider u li huma anqas minn sena mill-tlestija ta'qabel l-adjuvant' trastuzumab terapija bbażata fuq.

Tegsedi Unjoni Ewropea - Malti - EMA (European Medicines Agency)

tegsedi

akcea therapeutics ireland limited - inotersen sodium - amyloidosis - drogi oħra tas-sistema nervuża - it-trattament tal-fażi 1 jew l-istadju 2 polinewropatija f'pazjenti adulti b'ereditarji transthyretin amilojdożi (hattr).

Koselugo Unjoni Ewropea - Malti - EMA (European Medicines Agency)

koselugo

astrazeneca ab - selumetinib sulfate - neurofibromatosis 1 - aġenti antineoplastiċi - koselugo as monotherapy is indicated for the treatment of symptomatic, inoperable plexiform neurofibromas (pn) in paediatric patients with neurofibromatosis type 1 (nf1) aged 3 years and above.

Camcevi Unjoni Ewropea - Malti - EMA (European Medicines Agency)

camcevi

accord healthcare s.l.u. - leuprorelin mesilate - neoplasmi prostatiċi - terapija endokrinali - camcevi is indicated for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy.

Dabigatran Etexilate Accord Unjoni Ewropea - Malti - EMA (European Medicines Agency)

dabigatran etexilate accord

accord healthcare s.l.u. - dabigatran etexilate mesilate - venous thromboembolism; arthroplasty, replacement - aġenti antitrombotiċi - prevention of venous thromboembolic events.