EXFERANA 360MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

exferana 360mg potahovaná tableta

vipharm s.a., ożarów mazowiecki array - 16626 deferasirox - potahovaná tableta - 360mg - deferasirox

EXFERANA 90MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

exferana 90mg potahovaná tableta

vipharm s.a., ożarów mazowiecki polsko - 16626 deferasirox - potahovaná tableta - 90mg - deferasirox

Enerzair Breezhaler Evropská unie - čeština - EMA (European Medicines Agency)

enerzair breezhaler

novartis europharm limited - indacaterol, glycopyrronium bromide, mometasone - astma - léky na obstrukční onemocnění dýchacích cest, - enerzair breezhaler is indicated as a maintenance treatment of asthma in adult patients not adequately controlled with a maintenance combination of a long acting beta2 agonist and a high dose of an inhaled corticosteroid who experienced one or more asthma exacerbations in the previous year.

Zimbus Breezhaler Evropská unie - čeština - EMA (European Medicines Agency)

zimbus breezhaler

novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - astma - léky na obstrukční onemocnění dýchacích cest, - maintenance treatment of asthma in adults whose disease is not adequately controlled.

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

tecvayli

janssen-cilag international n.v. - teclistamab - mnohočetný myelom - antineoplastická činidla - tecvayli is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

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

tepkinly

abbvie deutschland gmbh & co. kg - epcoritamab - lymphoma, large b-cell, diffuse - antineoplastická činidla - tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) after two or more lines of systemic therapy.

Baycox Iron Evropská unie - čeština - EMA (European Medicines Agency)

baycox iron

bayer animal health gmbh - iron(iii) ion, toltrazuril - toltrazuril, kombinace - prasata (prasata) - za současné prevence klinických příznaků kokcidiózy (např. průjem) u novorozených selat na hospodářství s potvrzenou historii kokcidiózy způsobené cystoisospora suis, a prevenci nedostatku železa anémie.

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

felpreva

vétoquinol sa - emodepside, praziquantel, tigolaner - anthelmintika, - kočky - for cats with, or at risk from, mixed parasitic infestations. the veterinary medicinal product is exclusively indicated when ectoparasites, cestodes and nematodes are targeted at the same time.

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

carvykti

janssen-cilag international nv - ciltacabtagene autoleucel - mnohočetný myelom - carvykti is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

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

ebvallo

pierre fabre medicament - tabelecleucel - lymphoproliferative disorders - ebvallo is indicated as monotherapy for treatment of adult and paediatric patients 2 years of age and older with relapsed or refractory epstein-barr virus positive post-transplant lymphoproliferative disease (ebv+ ptld) who have received at least one prior therapy. for solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate.