Erbitux الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

erbitux

merck europe b.v.  - tsetuksimab - head and neck neoplasms; colorectal neoplasms - antineoplastilised ained - erbitux on näidustatud patsientide raviks epidermaalse kasvufaktori retseptori (egfr)-väljendades, ras metsikut tüüpi metastaatilise kolorektaalse vähi:koos irinotecan põhineva keemiaravi;esimene on-line kombinatsioonis folfox;ühe esindaja patsientidel, kes on jätnud oxaliplatin - ja irinotecan põhinev teraapia ja kes ei talu, et irinotecan. Üksikasju vaata punkt 5. erbitux on näidustatud ravi patsientidel, kellel on soomusrakuline rakkude vähk pea ja kaela:koos kiiritusravi puhul lokaalselt kaugelearenenud haigusega;koos platinum põhineva keemiaravi jaoks korduva ja/või metastaatilise haiguse.

Arzerra الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

arzerra

novartis europharm ltd - ofatumumab - leukeemia, lümfotsüütne, krooniline, b-rakk - monoklonaalsed antikehad - varem ravimata krooniline lümfoidne leukeemia (cll): arzerra koos kloorambutsiili või bendamustine on näidustatud patsientide raviks cll, kes ei ole eelnevalt saanud ravi ja kellel ei ole õigust fludarabine-põhine ravi. taastekkinud cll: arzerra on näidustatud kombinatsioonis fludarabine ja tsüklofosfamiidi ravi täiskasvanud patsientidel, kellel on taastekkinud cll. tulekindlad cll: arzerra on näidustatud ravi cll patsientidel, kes on tulekindlad, et fludarabine ja alemtuzumab.

Braftovi الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

braftovi

pierre fabre medicament - encorafenib - melanoma; colorectal neoplasms - antineoplastilised ained - encorafenib is indicated:in combination with binimetinib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutationin combination with cetuximab, for the treatment of adult patients with metastatic colorectal cancer (crc) with a braf v600e mutation, who have received prior systemic therapy.

Lumoxiti الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

lumoxiti

astrazeneca ab - moxetumomab pasudotox - leukeemia, karvane rakk - antineoplastilised ained - lumoxiti as monotherapy is indicated for the treatment of adult patients with relapsed or refractory hairy cell leukaemia (hcl) after receiving at least two prior systemic therapies, including treatment with a purine nucleoside analogue (pna).

Ebvallo الاتحاد الأوروبي - الإستونية - 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.

Dimethyl fumarate Mylan الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

dimethyl fumarate mylan

mylan ireland limited - dimetüülfumaraat - sclerosis multiplex, relapsing-remitting - immunosupressandid - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimethyl fumarate Polpharma الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

dimethyl fumarate polpharma

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dimetüülfumaraat - sclerosis multiplex, relapsing-remitting - immunosupressandid - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimethyl fumarate Neuraxpharm الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

dimethyl fumarate neuraxpharm

laboratorios lesvi s.l. - dimetüülfumaraat - sclerosis multiplex, relapsing-remitting - immunosupressandid - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Enjaymo الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

enjaymo

sanofi b.v. - sutimlimab - hemolysis; anemia, hemolytic, autoimmune - immunosupressandid - enjaymo is indicated for the treatment of haemolytic anaemia in adult patients with cold agglutinin disease (cad).

DIMTRUZIC gastroresistentne kõvakapsel أستونيا - الإستونية - Ravimiamet

dimtruzic gastroresistentne kõvakapsel

sandoz pharmaceuticals d.d. - dimetüülfumaraat - gastroresistentne kõvakapsel - 120mg 14tk