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

xerava

paion deutschland gmbh - eravacycline - infection; bacterial infections - antibatteriċi għal użu sistemiku, - xerava huwa indikat għall-kura ta ' infezzjonijiet intra-addominali kkumplikati (ciai) fl-adulti. għandha tingħata kunsiderazzjoni għall-gwida uffiċjali dwar l-użu xieraq ta ' sustanzi antibatteriċi.

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

tygacil

pfizer europe ma eeig - tigecycline - bacterial infections; skin diseases, bacterial; soft tissue infections - antibatteriċi għal użu sistemiku, - tygacil is indicated in adults and in children from the age of eight years for the treatment of the following infections: , complicated skin and soft tissue infections (cssti), excluding diabetic foot infections, complicated intra-abdominal infections (ciai) , tygacil should be used only in situations where other alternative antibiotics are not suitable. għandha tingħata kunsiderazzjoni għall-gwida uffiċjali dwar l-użu xieraq ta ' sustanzi antibatteriċi. l-użu xieraq ta ' sustanzi antibatteriċi.

Tigecycline Accord Unjoni Ewropea - Malti - EMA (European Medicines Agency)

tigecycline accord

accord healthcare s.l.u. - tigecycline - soft tissue infections; intraabdominal infections; bacterial infections; skin diseases, infectious - antibatteriċi għal użu sistemiku, - tygecycline qbil hija indikata fl-adulti u fit-tfal mill-età ta 'tmien snin għall-kura ta' l-infezzjonijiet li ġejjin (ara sezzjonijiet 4. 4 u 5. 1):infezzjonijiet kumplikati tal-ġilda u tat-tessuti rotob (cssti), esklużi l-infezzjonijiet dijabetiċi fis-saqajn (ara sezzjoni 4. 4)infezzjonijiet intra-addominali kkumplikati (ciai)tygecycline qbil għandu jintuża biss f'sitwazzjonijiet fejn l-alternattivi oħra l-antibijotiċi ma jkunux adattati (ara sezzjonijiet 4. 4, 4. 8 u 5. għandha tingħata kunsiderazzjoni għall-gwida uffiċjali dwar l-użu xieraq ta ' sustanzi antibatteriċi.

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

pombiliti

amicus therapeutics europe limited - cipaglucosidase alfa - mard tal-Ħażna tal-glukoġen tat-tip ii - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - pombiliti (cipaglucosidase alfa) is a long-term enzyme replacement therapy used in combination with the enzyme stabiliser miglustat for the treatment of adults with late-onset pompe disease (acid α-glucosidase [gaa] deficiency).

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

opfolda

amicus therapeutics europe limited - miglustat - mard tal-Ħażna tal-glukoġen tat-tip ii - prodotti oħra alimentari u metaboliżmu - opfolda (miglustat) is an enzyme stabiliser of cipaglucosidase alfa long-term enzyme replacement therapy in adults with late-onset pompe disease (acid α- glucosidase [gaa] deficiency).

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

revolade

novartis europharm limited - eltrombopag - purpura, tromboċitopenika, idjopatika - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 u 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 u 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

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

rebetol

merck sharp and dohme b.v - ribavirin - epatite Ċ, kronika - antivirals for systemic use, antivirals for treatment of hcv infections - rebetol huwa indikat flimkien ma 'prodotti mediċinali oħra għall-kura ta' l-epatite Ċ kronika (chc) fl-adulti. rebetol huwa indikat flimkien ma 'prodotti mediċinali oħra għat-trattament ta' epatite Ċ kronika (chc) għall-pazjenti pedjatriċi (minn tfal ta ' 3 snin jew akabr u adolexxenti) li ma kinux ittrattati qabel u mingħajr dikumpensazzjoni tal-fwied.

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

daklinza

bristol-myers squibb pharma eeig - daclatasvir dihydrochloride - epatite Ċ, kronika - antivirali għal użu sistemiku - daklinza huwa indikat flimkien ma 'prodotti mediċinali oħra għall-kura ta' infezzjoni kronika tal-virus tal-epatite Ċ (hcv) fl-adulti (ara sezzjonijiet 4. 2, 4. 4 u 5. għall-ġenotip hcv-attività speċifika, ara sezzjonijiet 4. 4 u 5.

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

enrylaze

jazz pharmaceuticals ireland limited - crisantaspase - leukimija limfoblastika taċ-Ċelluli prekursuri-linfoma - aġenti antineoplastiċi - enrylaze is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukaemia (all) and lymphoblastic lymphoma (lbl) in adult and paediatric patients (1 month and older) who developed hypersensitivity or silent inactivation to e. coli-derived asparaginase.

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.