LEFLUNOMID SANDOZ 20MG Potahovaná tableta Republik Czech - Czech - SUKL (Státní ústav pro kontrolu léčiv)

leflunomid sandoz 20mg potahovaná tableta

sandoz s.r.o., praha array - 8939 leflunomid - potahovaná tableta - 20mg - leflunomid

LEFLUNOPHARM 10MG Potahovaná tableta Republik Czech - Czech - SUKL (Státní ústav pro kontrolu léčiv)

leflunopharm 10mg potahovaná tableta

glenmark pharmaceuticals s.r.o., praha array - 8939 leflunomid - potahovaná tableta - 10mg - leflunomid

LEFLUNOPHARM 20MG Potahovaná tableta Republik Czech - Czech - SUKL (Státní ústav pro kontrolu léčiv)

leflunopharm 20mg potahovaná tableta

glenmark pharmaceuticals s.r.o., praha array - 8939 leflunomid - potahovaná tableta - 20mg - leflunomid

Jaypirca Kesatuan Eropah - Czech - EMA (European Medicines Agency)

jaypirca

eli lilly nederland b.v. - pirtobrutinib - lymfom, mantle-cell - inhibitory proteinkinázy - treatment of mantle cell lymphoma (mcl).

Tukysa Kesatuan Eropah - Czech - EMA (European Medicines Agency)

tukysa

seagen b.v. - tucatinib - breast neoplasms; neoplasm metastasis - antineoplastická činidla - tukysa is indicated in combination with trastuzumab and capecitabine for the treatment of adult patients with her2‑positive locally advanced or metastatic breast cancer who have received at least 2 prior anti‑her2 treatment regimens.

Vitrakvi Kesatuan Eropah - Czech - EMA (European Medicines Agency)

vitrakvi

bayer ag - larotrectinib sulfát - břišní novotvary - antineoplastická činidla - vitrakvi jako monoterapie je indikován k léčbě dospělých a pediatrických pacientů se solidními nádory, které vykazují neurotrofní receptor tyrosin kinázy (ntrk) fúzního genu,kteří mají nemoc, která je lokálně pokročilým, metastazujícím nebo kde chirurgická resekce, je pravděpodobné, že mít za následek závažné nemocnosti, která nemají žádné uspokojivé možnosti léčby.

Xenleta Kesatuan Eropah - Czech - EMA (European Medicines Agency)

xenleta

nabriva therapeutics ireland dac - lefamulin acetate - pneumonia, bacterial; community-acquired infections - antibakteriální látky pro systémové použití, - xenleta is indicated for the treatment of community-acquired pneumonia (cap) in adults when it is considered inappropriate to use antibacterial agents that are commonly recommended for the initial treatment of cap or when these have failed. pozornost by měla být věnována oficiálním doporučením pro správné používání antibakteriálních látek.

Aubagio Kesatuan Eropah - Czech - EMA (European Medicines Agency)

aubagio

sanofi winthrop industrie - teriflunomid - roztroušená skleróza - selektivní imunosupresiva - aubagio is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Teriflunomide Mylan Kesatuan Eropah - Czech - EMA (European Medicines Agency)

teriflunomide mylan

mylan pharmaceuticals limited - teriflunomid - roztroušená skleróza, relaps-remitentní - imunosupresiva - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).

Teriflunomide Accord Kesatuan Eropah - Czech - EMA (European Medicines Agency)

teriflunomide accord

accord healthcare s.l.u. - teriflunomid - roztroušená skleróza, relaps-remitentní - imunosupresiva, selektivní imunosupresiva - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).