Thiotepa Riemser Unjoni Ewropea - Malti - EMA (European Medicines Agency)

thiotepa riemser

esteve pharmaceuticals gmbh - thiotepa - hematopoietic stem cell transplantation; neoplasms - aġenti antineoplastiċi - thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients. thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients.

Temozolomide Hexal Unjoni Ewropea - Malti - EMA (European Medicines Agency)

temozolomide hexal

hexal ag - temozolomide - glioma; glioblastoma - aġenti antineoplastiċi - għat-trattament ta 'pazjenti adulti b'glioblastoma multiforme dijanjostikata fl-istess ħin ma' radjuterapija (rt) u sussegwentement bħala trattament b'monoterapija. għall-kura tat-tfal mill-età ta ' tliet snin fuq, adolexxenti, u pazjenti adulti bi glijoma malinna, bħal glioblastoma multiforme jew astroċitoma anaplastika, li jerġgħu jirkadu jew progressjoni wara terapija standard.

Replagal Unjoni Ewropea - Malti - EMA (European Medicines Agency)

replagal

takeda pharmaceuticals international ag ireland branch - agalsidase alfa - marda ta 'fabry - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - replagal huwa indikat għal terapija fit-tul ta 'sostituzzjoni enżimika f'pazjenti b'dijanjosi kkonfermata ta' marda ta 'fabry (defiċjenza ta' α-galaktosidase-a).

Lunsumio Unjoni Ewropea - Malti - EMA (European Medicines Agency)

lunsumio

roche registration gmbh - mosunetuzumab - limfoma, follicular - antineoplastic agents, monoclonal antibodies - lunsumio as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (fl) who have received at least two prior systemic therapies.

Solymbic Unjoni Ewropea - Malti - EMA (European Medicines Agency)

solymbic

amgen europe b.v. - adalimumab - arthritis, psoriatic; spondylitis, ankylosing; crohn disease; colitis, ulcerative; hidradenitis suppurativa; psoriasis; arthritis, rheumatoid - immunosoppressanti - jekk jogħġbok irreferi għas-sezzjoni 4. 1 tas-sommarju tal-karatteristiċi tal-prodott fid-dokument ta 'informazzjoni tal-prodott.

Helicobacter Test INFAI Unjoni Ewropea - Malti - EMA (European Medicines Agency)

helicobacter test infai

infai, institut für biomedizinische analytik nmr-imaging gmbh - urea (13c) - breath tests; helicobacter infections - aġenti dijanjostiċi - helicobacter test infai jista 'jintuża għal dijanjosi in vivo ta' infezzjoni ta 'helicobacter pylori gastroduwodenali fl:adulti;l-adoloxxenti, li aktarx ikollhom mard ta' ulċeri peptiċi. helicobacter test infai għal tfal bejn l-etajiet minn tlieta sa 11-il sena jista 'jintuża għal dijanjosi in vivo ta gastrduodenal infezzjoni ta' helicobacter pylori:għall-evalwazzjoni tas-suċċess tal-qerda tal-kura, jew meta testijiet invażivi ma jistgħux jiġu mwettqa, jew;meta jkun hemm riżultati konfliġġenti li joħorġu mit-testijiet invażivi. dan il-prodott mediċinali huwa għal użu dijanjostiku biss.

Humira Unjoni Ewropea - Malti - EMA (European Medicines Agency)

humira

abbvie deutschland gmbh co. kg - adalimumab - spondylitis, ankylosing; arthritis, juvenile rheumatoid; uveitis; colitis, ulcerative; psoriasis; arthritis, psoriatic; crohn disease; arthritis, rheumatoid - immunosoppressanti - jekk jogħġbok irreferi għad-dokument ta 'informazzjoni dwar il-prodott.

Okedi Unjoni Ewropea - Malti - EMA (European Medicines Agency)

okedi

laboratorios farmacéuticos rovi, s.a. - risperidone - skizofrenija - psikolettiċi - treatment of schizophrenia in adults for whom tolerability and effectiveness has been established with oral risperidone.

Quviviq Unjoni Ewropea - Malti - EMA (European Medicines Agency)

quviviq

idorsia pharmaceuticals deutschland gmbh - daridorexant hydrochloride - sleep inizjattiva u maintenance disorders - psikolettiċi - quviviq is indicated for the treatment of adult patients with insomnia characterised by symptoms present for at least 3 months and considerable impact on daytime functioning.

Temozolomide Teva Unjoni Ewropea - Malti - EMA (European Medicines Agency)

temozolomide teva

teva b.v.  - temozolomide - glioma; glioblastoma - aġenti antineoplastiċi - għat-trattament ta 'pazjenti adulti b'glioblastoma multiforme dijanjostikata fl-istess ħin ma' radjuterapija (rt) u sussegwentement bħala trattament b'monoterapija. għall-kura tat-tfal mill-età ta ' tliet snin fuq, adolexxenti, u pazjenti adulti bi glijoma malinna, bħal glioblastoma multiforme jew astroċitoma anaplastika, li jerġgħu jirkadu jew progressjoni wara terapija standard.