Cibinqo Európai Unió - máltai - EMA (European Medicines Agency)

cibinqo

pfizer europe ma eeig  - abrocitinib - dermatite, atopika - preparazzjonijiet oħra dermatoloġiċi - cibinqo is indicated for the treatment of moderate-to-severe atopic dermatitis in adults who are candidates for systemic therapy.

Gavreto Európai Unió - máltai - EMA (European Medicines Agency)

gavreto

roche registration gmbh  - pralsetinib - karċinoma, pulmun mhux taċ-Ċellula Żgħira - aġenti antineoplastiċi - gavreto is indicated as monotherapy for the treatment of adult patients with rearranged during transfection (ret) fusion-positive advanced non-small cell lung cancer (nsclc) not previously treated with a ret inhibitor.

Kerendia Európai Unió - máltai - EMA (European Medicines Agency)

kerendia

bayer ag - finerenone - renal insufficiency, chronic; diabetes mellitus, type 2 - aġenti li jaġixxu fuq is-sistema renin-angiotensin - kerendia is indicated for the treatment of chronic kidney disease (stage 3 and 4 with albuminuria) associated with type 2 diabetes in adults.

Okedi Európai Unió - máltai - EMA (European Medicines Agency)

okedi

laboratorios farmacéuticos rovi, s.a. - risperidone - skizofrenija - psikolettiċi - treatment of schizophrenia in adults for whom tolerability and effectiveness has been established with oral risperidone.

Pirfenidone axunio (previously Pirfenidone AET) Európai Unió - máltai - EMA (European Medicines Agency)

pirfenidone axunio (previously pirfenidone aet)

axunio pharma gmbh - pirfenidone - fibrożi pulmonari idjopatika - immunosoppressanti - pirfenidone aet is indicated in adults for the treatment of mild to moderate idiopathic pulmonary fibrosis (ipf).

Melatonin Neurim Európai Unió - máltai - EMA (European Medicines Agency)

melatonin neurim

rad neurim pharmaceuticals eec sarl - melatonin - sleep inizjattiva u maintenance disorders - psikolettiċi - melatonin neurim is indicated as monotherapy for the short-term treatment of primary insomnia characterised by poor quality of sleep in patients who are aged 55 or over.

Pirfenidone Viatris Európai Unió - máltai - EMA (European Medicines Agency)

pirfenidone viatris

viatris limited - pirfenidone - idiopathic pulmonary fibrosis; lung diseases; respiratory tract diseases - immunosoppressanti - pirfenidone viatris is indicated in adults for the treatment of mild to moderate idiopathic pulmonary fibrosis (ipf).

Orserdu Európai Unió - máltai - EMA (European Medicines Agency)

orserdu

stemline therapeutics b.v. - elacestrant - neoplażmi tas-sider - terapija endokrinali - orserdu monotherapy is indicated for the treatment of postmenopausal women, and men, with estrogen receptor (er) positive, her2-negative, locally advanced or metastatic breast cancer with an activating esr1 mutation who have disease progression following at least one line of endocrine therapy including a cdk 4/6 inhibitor.

Pheburane Európai Unió - máltai - EMA (European Medicines Agency)

pheburane

eurocept international b. v. - sodium phenylbutyrate - carbamoyl-fosfat synthase i marda defiċjenza - varji ta'l-apparat alimentari u tal-metaboliżmu-prodotti - it-trattament kroniku tal-ġestjoni tal-urea-disturbi fiċ-ċiklu.

Imprida HCT Európai Unió - máltai - EMA (European Medicines Agency)

imprida hct

novartis europharm ltd. - l-amlodipina, valsartan, hydrochlorothiazide - pressjoni għolja - antagonisti ta 'angiotensin ii, sempliċi, antagonisti ta' angiotensin ii, kombinazzjonijiet - trattament ta ' l-ipertensjoni essenzjali bħala terapija ta ' sostituzzjoni fil-pazjenti adulti l-pressjoni tad-demm tagħhom huwa kontrollat adegwatament dwar il-kombinazzjoni ta ' amlodipine, valsartan u idrochlorothiazide (hct), meħuda bħala tliet formulazzjonijiet ta ' wieħed il-komponent jew bħala a doppju-komponent u formulazzjoni wieħed-komponent.