Unjoni Ewropea - Malti - EMA (European Medicines Agency)

pfizer europe ma eeig - nirmatrelvir, ritonavir - covid-19 virus infection - paxlovid is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who do not require supplemental oxygen and who are at increased risk for progressing to severe covid 19.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

siga technologies netherlands b.v. - tecovirimat - poxviridae infections; cowpox; monkeypox; vaccinia; smallpox - antivirali għal użu sistemiku - tecovirimat siga is indicated for the treatment of the following viral infections in adults and children with body weight at least 13 kg:- smallpox- monkeypox- cowpoxtecovirimat siga is also indicated to treat complications due to replication of vaccinia virus following vaccination against smallpox in adults and children with body weight at least 13 kg (see sections 4. 4 u 5. tecovirimat siga should be used in accordance with official recommendations.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

accord healthcare s.l.u. - relugolix - neoplasmi prostatiċi - terapija endokrinali - orgovyx is indicated for the treatment of adult patients with advanced hormone-sensitive prostate cancer.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm limited - asciminib hydrochloride - lewkimja, mjeloġenika, kronika, bcr-abl pożittiva - aġenti antineoplastiċi - scemblix is indicated for the treatment of adult patients with philadelphia chromosome positive chronic myeloid leukaemia in chronic phase (ph+ cml cp) previously treated with two or more tyrosine kinase inhibitors (see section 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

les laboratoires servier - ivosidenib - leukemia, myeloid, acute; cholangiocarcinoma - aġenti antineoplastiċi - tibsovo in combination with azacitidine is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (aml) with an isocitrate dehydrogenase-1 (idh1) r132 mutation who are not eligible to receive standard induction chemotherapy (see section 5. tibsovo monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with an idh1 r132 mutation who were previously treated by at least one prior line of systemic therapy.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

accord healthcare s.l.u. - degarelix acetate - neoplasmi prostatiċi - other hormone antagonists and related agents - degarelix accord is a gonadotrophin releasing hormone (gnrh) antagonist indicated:for treatment of adult male patients with advanced hormone-dependent prostate cancer. for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

roche registration gmbh - baloxavir marboxil - influwenza, bniedem - antivirali għal użu sistemiku - treatment of influenzaxofluza is indicated for the treatment of uncomplicated influenza in patients aged 1 year and above. post exposure prophylaxis of influenzaxofluza is indicated for post-exposure prophylaxis of influenza in individuals aged 1 year and above. xofluza should be used in accordance with official recommendations.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

basilea pharmaceutica deutschland gmbh - isavuconazole - asperġillożi - cresemba huwa indikat fl-adulti għall-kura ta': invażivi aspergillosismucormycosis fil-pazjenti li għalihom amphotericin b huwa inappropriateconsideration għandha tingħata lill-gwida uffiċjali dwar l-użu xieraq ta ' mediċini antifungali.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

teva b.v.  - sildenafil - disfunzjoni erettili - drogi użati f'każ ta 'disfunzjoni erettili - trattament ta 'rġiel b'funzjoni ta' disfunzjoni erettili, li hija l-inkapaċità li tikseb jew iżżomm erezzjoni tal-pene suffiċjenti għal prestazzjoni sesswali sodisfaċenti. sabiex għal sildenafil teva ikun effettiv, hija meħtieġa stimulazzjoni sesswali.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

actavis group ptc ehf - sildenafil - disfunzjoni erettili - uroloġiċi - trattament ta 'rġiel b'funzjoni ta' disfunzjoni erettili, li hija l-inkapaċità li tikseb jew iżżomm erezzjoni tal-pene suffiċjenti għal prestazzjoni sesswali sodisfaċenti. sabiex għal sildenafil actavis ikun effettiv, hija meħtieġa stimulazzjoni sesswali.