Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - anakinra - arthritis, rheumatoid; covid-19 virus infection - immunsuppressiva - rheumatoid arthritis (ra)kineret is indicated in adults for the treatment of the signs and symptoms of ra in combination with methotrexate, with an inadequate response to methotrexate alone. covid-19kineret is indicated for the treatment of coronavirus disease 2019 (covid-19) in adult patients with pneumonia requiring supplemental oxygen (low- or high-flow oxygen) who are at risk of progressing to severe respiratory failure determined by plasma concentration of soluble urokinase plasminogen activator receptor (supar) ≥ 6 ng/ml. periodisk feber syndromeskineret är indicerat för behandling av följande autoinflammatoriskt periodisk feber syndrom hos vuxna, ungdomar, barn och spädbarn i åldern 8 månader och äldre med en kroppsvikt på 10 kg eller däröver:cryopyrin-associerad periodiskt syndrom (caps)kineret är indicerat för behandling av caps, inklusive:neonatal debut multisystem inflammatoriska sjukdomar (nomid) / kronisk infantila neurologiska, kutan, articular syndrome (cinca)muckle-wells syndrom (mws)familjär kalla autoinflammatoriskt syndrom (fcas)familjär medelhavs feber (fmf)kineret är indicerat för behandling av familjär medelhavs feber (fmf). kineret ska ges i kombination med kolkicin, om det är lämpligt. still’s diseasekineret is indicated in adults, adolescents, children and infants aged 8 months and older with a body weight of 10 kg or above for the treatment of still’s disease, including systemic juvenile idiopathic arthritis (sjia) and adult-onset still’s disease (aosd), with active systemic features of moderate to high disease activity, or in patients with continued disease activity after treatment with non-steroidal anti-inflammatory drugs (nsaids) or glucocorticoids. kineret can be given as monotherapy or in combination with other anti-inflammatory drugs and disease-modifying antirheumatic drugs (dmards).

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

swedish orphan biovitrum ab - kollagenas clostridium histolyticum - dupuytren kontrakt - andra droger för sjukdomar i muskel-skelettsystemet - , the treatment of dupuytren’s contracture in adult patients with a palpable cord. behandling av vuxna män med peyronies sjukdom med en påtaglig plack och krökning deformitet av minst 30 grader i början av terapi.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

sanofi b.v. - tyrotropin alfa - sköldkörtelnoplasmer - främre hypofys lob hormoner och analoger, hypofysen och hypotalamus hormoner och derivat - thyrogen is indicated for use with serum thyroglobulin (tg) testing with or without radioiodine imaging for the detection of thyroid remnants and well-differentiated thyroid cancer in post thyroidectomy patients maintained on hormone suppression therapy (thst). low risk patients with well-differentiated thyroid carcinoma who have undetectable serum tg levels on thst and no rh (recombinant human) tsh-stimulated increase of tg levels may be followed-up by assaying rh tsh-stimulated tg levels. thyrogen is indicated for pre-therapeutic stimulation in combination with a range of 30 mci (1. 1 gbq) to 100 mci (3. 7 gbq) radioiodine for ablation of thyroid tissue remnants in patients who have undergone a near-total or total thyroidectomy for well-differentiated thyroid cancer and who do not have evidence of distant metastatic thyroid cancer (see section 4.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - avatrombopag maleate - trombocytopeni - hemostatika - doptelet är indicerat för behandling av svår trombocytopeni hos vuxna patienter med kronisk leversjukdom som är planerade att genomgå ett ingrepp. doptelet is indicated for the treatment of primary chronic immune thrombocytopenia (itp) in adult patients who are refractory to other treatments (e. kortikosteroider, immunoglobuliner).

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - emapalumab - immune system diseases - gamifant is indicated for the treatment of paediatric patients aged under 18 years with primary haemophagocytic lymphohistiocytosis (hlh).

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

swedish orphan biovitrum ab - loncastuximab tesirine - lymphoma, large b-cell, diffuse; lymphoma, b-cell - antineoplastiska medel - zynlonta as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl), after two or more lines of systemic therapy.

Thụy Điển - Tiếng Thụy Điển - Läkemedelsverket (Medical Products Agency)

chemvet dk a/s - actinobacillus pleuropneumoniae, apxi-toxoid; actinobacillus pleuropneumoniae, apxii-toxoid; actinobacillus pleuropneumoniae, apxiii-toxoid; actinobacillus pleuropneumoniae, serotyp 2, stam app2tr98, inaktiverad; actinobacillus pleuropneumoniae, serotyp 9, stam app9tr97, inaktiverad - injektionsvätska, emulsion - actinobacillus pleuropneumoniae, serotyp 2, stam app2tr98, inaktiverad 1 - 10 e aktiv substans; emulsigen sa 0,36 ml adjuvans; saponin 0,1 mg adjuvans; actinobacillus pleuropneumoniae, apxiii-toxoid 1 - 10 e aktiv substans; formaldehyd hjälpämne; tiomersal hjälpämne; actinobacillus pleuropneumoniae, apxi-toxoid 1 - 10 e aktiv substans; actinobacillus pleuropneumoniae, apxii-toxoid 1 - 10 e aktiv substans; actinobacillus pleuropneumoniae, serotyp 9, stam app9tr97, inaktiverad 1 - 10 e aktiv substans - svin

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

teva pharma b.v. - rivastigmin - dementia; alzheimer disease; parkinson disease - kolinesterashämmare - symtomatisk behandling av mild till måttligt svår alzheimers demens. symtomatisk behandling av mild till måttligt svår demens hos patienter med idiopatisk parkinsons sjukdom.

Thụy Điển - Tiếng Thụy Điển - Läkemedelsverket (Medical Products Agency)

vale pharmaceuticals ltd - ibuprofennatriumdihydrat; paracetamol - infusionsvätska, lösning - 10 mg/ml+3 mg/ml - ibuprofennatriumdihydrat 3,85 mg aktiv substans; mannitol hjälpämne; paracetamol 10 mg aktiv substans

Thụy Điển - Tiếng Thụy Điển - Läkemedelsverket (Medical Products Agency)

vale pharmaceuticals ltd - ibuprofennatriumdihydrat; paracetamol - infusionsvätska, lösning - 10 mg/ml+3 mg/ml - paracetamol 10 mg aktiv substans; mannitol hjälpämne; ibuprofennatriumdihydrat 3,85 mg aktiv substans