Europeiska unionen - svenska - EMA (European Medicines Agency)

astrazeneca ab - moxetumomab pasudotox - leukemi, hårig cell - antineoplastiska medel - 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).

Europeiska unionen - svenska - EMA (European Medicines Agency)

resilience biomanufacturing ireland limited - influensavaccin (helvirion, inaktiverad) innehållande antigen av: a / vietnam / 1203/2004 (h5n1) - influenza, human; immunization; disease outbreaks - vacciner - profylax av influensa i en officiellt deklarerad pandemisk situation. pandemiskt influensavaccin ska användas enligt officiell vägledning.

Europeiska unionen - svenska - EMA (European Medicines Agency)

pfizer europe ma eeig - tofacitinib - artrit, reumatoid - immunsuppressiva - 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 och 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.

Europeiska unionen - svenska - EMA (European Medicines Agency)

gilead sciences ireland uc, galapagos nv - filgotinib maleate - artrit, reumatoid - immunsuppressiva - rheumatoid arthritisjyseleca is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease modifying anti rheumatic drugs (dmards). jyseleca may be used as monotherapy or in combination with methotrexate (mtx). ulcerative colitisjyseleca is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic agent.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

medical valley invest ab - erlotinibhydroklorid - filmdragerad tablett - 25 mg - natriumlaurilsulfat hjälpämne; erlotinibhydroklorid 27,317 mg aktiv substans; laktosmonohydrat hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

medical valley invest ab - erlotinibhydroklorid - filmdragerad tablett - 150 mg - laktosmonohydrat hjälpämne; natriumlaurilsulfat hjälpämne; erlotinibhydroklorid 163,9 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

medical valley invest ab - erlotinibhydroklorid - filmdragerad tablett - 100 mg - laktosmonohydrat hjälpämne; erlotinibhydroklorid 109,267 mg aktiv substans; natriumlaurilsulfat hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - esomeprazolnatrium - pulver till injektions-/infusionsvätska, lösning - 40 mg - esomeprazolnatrium 42,5 mg aktiv substans - esomeprazol

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - esomeprazolnatrium - pulver till injektions-/infusionsvätska, lösning - 40 mg - esomeprazolnatrium 42,5 mg aktiv substans - esomeprazol

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - esomeprazolnatrium - pulver till injektions-/infusionsvätska, lösning - 40 mg - esomeprazolnatrium 42,5 mg aktiv substans - esomeprazol