Reagila Evropská unie - čeština - EMA (European Medicines Agency)

reagila

gedeon richter - kariprazin hydrochlorid - schizofrenie - psycholeptika - přípravek reagila je indikován k léčbě schizofrenie u dospělých pacientů.

PREATO 150MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

preato 150mg tableta

neuraxpharm bohemia s.r.o., praha array - 15519 pregabalin - tableta - 150mg - pregabalin

PREATO 300MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

preato 300mg tableta

neuraxpharm bohemia s.r.o., praha array - 15519 pregabalin - tableta - 300mg - pregabalin

PREATO 75MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

preato 75mg tableta

neuraxpharm bohemia s.r.o., praha array - 15519 pregabalin - tableta - 75mg - pregabalin

Trulicity Evropská unie - čeština - EMA (European Medicines Agency)

trulicity

eli lilly nederland b.v. - dulaglutid - diabetes mellitus, typ 2 - drugs used in diabetes, blood glucose lowering drugs, excl. insulins - trulicity is indicated for the treatment of patients 10 years and above with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes. pro výsledky studií s ohledem na kombinace, účinky na kontrolu glykémie a kardiovaskulárních příhod, a populace studoval, viz bod 4. 4, 4. 5 a 5.

Libtayo Evropská unie - čeština - EMA (European Medicines Agency)

libtayo

regeneron ireland designated activity company (dac) - cemiplimab - karcinom, skvamózní buňka - antineoplastická činidla - 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.

Sunlenca Evropská unie - čeština - EMA (European Medicines Agency)

sunlenca

gilead sciences ireland unlimited company - lenacapavir sodium - hiv infekce - antivirotika pro systémové použití - sunlenca injection, in combination with other antiretroviral(s), is indicated for the treatment of adults with multidrug resistant hiv 1 infection for whom it is otherwise not possible to construct a suppressive anti viral regimen (see sections 4. 2 a 5. sunlenca tablet, in combination with other antiretroviral(s), is indicated for the treatment of adults with multidrug resistant hiv 1 infection for whom it is otherwise not possible to construct a suppressive anti viral regimen, for oral loading prior to administration of long-acting lenacapavir injection (see sections 4. 2 a 5.

TESTAVAN 20MG/G Transdermální gel Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

testavan 20mg/g transdermální gel

the simple pharma company limited, dublin array - 1422 testosteron - transdermální gel - 20mg/g - testosteron

Angiox Evropská unie - čeština - EMA (European Medicines Agency)

angiox

the medicines company uk ltd - bivalirudin - akutní koronární syndrom - antitrombotické činidla - angiox je indikován jako antikoagulancium v dospělých pacientů, kteří podstupují perkutánní koronární zákrok (pci) včetně pacientů s st-segment elevation myocardial infarction (stemi), kteří podstupují primární pci. angiox je také indikován k léčbě dospělých pacientů s nestabilní anginou / non-st-segment-v případě infarktu myokardu s elevací (ua / nstemi) plánované k neodkladné nebo včasné intervence. přípravek angiox by měl být podáván společně s aspirinem a klopidogrelem.

Recuvyra Evropská unie - čeština - EMA (European Medicines Agency)

recuvyra

eli lilly and company limited  - fentanyl - nervový systém - psi - pro kontrolu bolesti spojené s ortopedickou operací a operací měkkých tkání u psů.