Midazolam Baxter 1 mg/ml Słowacja - słowacki - ŠÚKL (Štátny ústav pre kontrolu liečiv)

midazolam baxter 1 mg/ml

baxter deutschland gmbh, nemecko - midazolam - 57 - hypnotica, sedativa

Trepulmix Unia Europejska - słowacki - EMA (European Medicines Agency)

trepulmix

scipharm sàrl - treprostinil sodíka - hypertenzia, pľúca - antitrombotické činidlá - treatment of adult patients with who functional class (fc) iii or iv and:inoperable chronic thromboembolic pulmonary hypertension (cteph), orpersistent or recurrent cteph after surgical treatmentto improve exercise capacity.

Oxlumo Unia Europejska - słowacki - EMA (European Medicines Agency)

oxlumo

alnylam netherlands b.v. - lumasiran sodium - hyperoxaluria, primary - iné alimentárny trakt a metabolizmus výrobky, - treatment of primary hyperoxaluria type 1 (ph1) in all age groups.

HUSAR STAR Słowacja - słowacki - myHealthbox

husar star

bayer ag - vodou dispergovateľný granulát - iodosulfuron-methyl-sodium 33 g/kg; thiencarbazone-methyl 25 g/kg; mefenpyr-diethy (safener) 150 g/kg

SEKATOR PLUS Słowacja - słowacki - myHealthbox

sekator plus

bayer ag - suspenzný koncentrát - amidosulfuron 25 g/l; iodosulfuron-methyl-sodium 6,25 g/l; 2,4-d 2-ehe 433 g/l; mefenpyr-diethyl (safener) 62,5 g/l

Sugammadex Mylan Unia Europejska - słowacki - EMA (European Medicines Agency)

sugammadex mylan

mylan ireland limited - sugammadex sodium - neuromuskulárna blokáda - všetky ostatné terapeutické produkty - reversal of neuromuscular blockade induced by   rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Fresenius Kabi Unia Europejska - słowacki - EMA (European Medicines Agency)

sugammadex fresenius kabi

fresenius kabi deutschland gmbh - sugammadex sodium - neuromuskulárna blokáda - všetky ostatné terapeutické produkty - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sunlenca Unia Europejska - słowacki - EMA (European Medicines Agency)

sunlenca

gilead sciences ireland unlimited company - lenacapavir sodium - hiv infekcie - antivirotiká na systémové použitie - 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.

Amvuttra Unia Europejska - słowacki - EMA (European Medicines Agency)

amvuttra

alnylam netherlands b.v. - vutrisiran sodium - amyloid neuropathies, familial - Ďalšie lieky na nervový systém - treatment of hereditary transthyretin-mediated amyloidosis (hattr amyloidosis) in adult patients with stage 1 or stage 2 polyneuropathy.

Sugammadex Amomed Unia Europejska - słowacki - EMA (European Medicines Agency)

sugammadex amomed

aop orphan pharmaceuticals gmbh - sugammadex sodium - neuromuskulárna blokáda - všetky ostatné terapeutické produkty - zvrat neuromuskulárnej blokády indukovanej rokurónom alebo vekuróniom. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.