Cộng hòa Séc - Tiếng Séc - SUKL (Státní ústav pro kontrolu léčiv)

viatris healthcare limited, dublin array - 4352 fenofibrÁt - potahovaná tableta - 215mg - fenofibrÁt

Cộng hòa Séc - Tiếng Séc - SUKL (Státní ústav pro kontrolu léčiv)

viatris healthcare limited, dublin array - 4352 fenofibrÁt - potahovaná tableta - 145mg - fenofibrÁt

Cộng hòa Séc - Tiếng Séc - SUKL (Státní ústav pro kontrolu léčiv)

viatris healthcare limited, dublin array - 4352 fenofibrÁt - tvrdá tobolka - 267mg - fenofibrÁt

Cộng hòa Séc - Tiếng Séc - SUKL (Státní ústav pro kontrolu léčiv)

viatris healthcare limited, dublin array - 4352 fenofibrÁt - potahovaná tableta - 160mg - fenofibrÁt

Liên Minh Châu Âu - Tiếng Séc - EMA (European Medicines Agency)

amgen technology (ireland) uc - ekulizumab - hemoglobinurie, paroxysmální - imunosupresiva - bekemv is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). důkazy o klinické prospěšnosti je prokázána u pacientů s hemolýza s klinickým příznakem(s) svědčí o vysoké aktivity nemoci, bez ohledu na to, transfúze historie (viz bod 5.

Liên Minh Châu Âu - Tiếng Séc - EMA (European Medicines Agency)

pfizer europe ma eeig - tofacitinib - artritida, revmatoidní - imunosupresiva - rheumatoid arthritistofacitinib in combination with methotrexate (mtx) is indicated for the treatment of moderate to severe active rheumatoid arthritis (ra) in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying antirheumatic drugs (dmards) (see section 5. tofacitinib can be given as monotherapy in case of intolerance to mtx or when treatment with mtx is inappropriate (see sections 4. 4 a 4. psoriatic arthritistofacitinib in combination with mtx is indicated for the treatment of active psoriatic arthritis (psa) in adult patients who have had an inadequate response or who have been intolerant to a prior disease modifying antirheumatic drug (dmard) therapy (see section 5. ulcerative colitistofacitinib is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent (see section 5. tofacitinib is indicated for the treatment of active polyarticular juvenile idiopathic arthritis (rheumatoid factor positive [rf+] or negative [rf-] polyarthritis and extended oligoarthritis), and juvenile psoriatic arthritis (psa) in patients 2 years of age and older, who have responded inadequately to previous therapy with disease modifying antirheumatic drugs (dmards). tofacitinib can be given in combination with methotrexate (mtx) or as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. ankylosing spondylitistofacitinib is indicated for the treatment of adult patients with active ankylosing spondylitis (as) who have responded inadequately to conventional therapy.

Cộng hòa Séc - Tiếng Séc - SUKL (Státní ústav pro kontrolu léčiv)

janssen-cilag s.r.o., praha array - 2220 fentanyl - transdermální náplast - 100mcg/h - fentanyl

Cộng hòa Séc - Tiếng Séc - SUKL (Státní ústav pro kontrolu léčiv)

janssen-cilag s.r.o., praha array - 2220 fentanyl - transdermální náplast - 12mcg/h - fentanyl

Cộng hòa Séc - Tiếng Séc - SUKL (Státní ústav pro kontrolu léčiv)

janssen-cilag s.r.o., praha array - 2220 fentanyl - transdermální náplast - 25mcg/h - fentanyl

Cộng hòa Séc - Tiếng Séc - SUKL (Státní ústav pro kontrolu léčiv)

janssen-cilag s.r.o., praha array - 2220 fentanyl - transdermální náplast - 50mcg/h - fentanyl