REDITENS 180 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

reditens 180 mg

pharos mt ltd. - malta - deferasiroxum - compr. film. - 180mg - alte preparate terapeutice chelatori de fer

REDITENS 360 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

reditens 360 mg

pharos mt ltd. - malta - deferasiroxum - compr. film. - 360mg - alte preparate terapeutice chelatori de fer

REDITENS 90 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

reditens 90 mg

pharos mt ltd. - malta - deferasiroxum - compr. film. - 90mg - alte preparate terapeutice chelatori de fer

MAYSIGLU 100 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

maysiglu 100 mg

krka, d.d., novo mesto - slovenia - sitagliptinum - compr. film. - 100mg - analogi ai glp-1 inhibitori ai dipeptidil peptidazei 4 (dpp-4)

MAYSIGLU 25 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

maysiglu 25 mg

krka, d.d., novo mesto - slovenia - sitagliptinum - compr. film. - 25mg - analogi ai glp-1 inhibitori ai dipeptidil peptidazei 4 (dpp-4)

MAYSIGLU 50 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

maysiglu 50 mg

krka, d.d., novo mesto - slovenia - sitagliptinum - compr. film. - 50mg - analogi ai glp-1 inhibitori ai dipeptidil peptidazei 4 (dpp-4)

NEBIVOLOL TORRENT 5 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

nebivolol torrent 5 mg

heumann pharma gmbh & co. generica kg - germania - nebivololum - compr. - 5mg - agenti betablocanti betablocante selective

ETRIXENAL 250 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

etrixenal 250 mg

walmark, a.s. - republica ceha - naproxenum - compr. - 250mg - antiinflamatoare si antireumatice nesteroidiene derivati de acid propionic

Libtayo Uniunea Europeană - română - EMA (European Medicines Agency)

libtayo

regeneron ireland designated activity company (dac) - cemiplimab - carcinom, celule scuamoase - agenți antineoplazici - cutaneous squamous cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma (mcscc or lacscc) who are not candidates for curative surgery or curative radiation. basal cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic basal cell carcinoma (labcc or mbcc) who have progressed on or are intolerant to a hedgehog pathway inhibitor (hhi). non-small cell lung cancerlibtayo as monotherapy is indicated for the first-line treatment of adult patients with non-small cell lung cancer (nsclc) expressing pd-l1 (in ≥ 50% tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. libtayo in combination with platinum‐based chemotherapy is indicated for the first‐line treatment of adult patients with nsclc expressing pd-l1 (in ≥ 1% of tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. cervical cancerlibtayo as monotherapy is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer and disease progression on or after platinum-based chemotherapy.

Helixate NexGen Uniunea Europeană - română - EMA (European Medicines Agency)

helixate nexgen

bayer ag  - octocog alfa - hemofilia a - hemostatice - tratamentul și profilaxia hemoragiei la pacienții cu hemofilie a (deficit congenital de factor viii). acest preparat nu conține factorul von willebrand și este, prin urmare, nu este indicat în boala von willebrand.