Sverige - svenska - Läkemedelsverket (Medical Products Agency)

evolan pharma ab - digoxin - injektionsvätska, lösning - 0,25 mg/ml - digoxin 0,25 mg aktiv substans; propylenglykol hjälpämne; etanol, vattenfri hjälpämne - digoxin

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

glaxosmithkline ab - varicellavirus, stam oka, levande försvagat - pulver och vätska till injektionsvätska, lösning - mannitol hjälpämne; fenylalanin hjälpämne; varicellavirus, stam oka, levande försvagat 3,3 log10 pfu aktiv substans; sorbitol hjälpämne; laktos (vattenfri) hjälpämne - levande försvagat

Europeiska unionen - svenska - EMA (European Medicines Agency)

zoetis belgium sa - synthetic peptide analogue of gnrf conjugated to diptheria toxoid - immunologiska medel för suidae - male pigs (from 8 weeks of age); female pigs (from 14 weeks of age) - male pigs:induction of antibodies against gnrf to produce a temporary immunological suppression of testicular function. for use as an alternative to physical castration for the reduction of boar taint caused by the key boar taint compound androstenone, in entire male pigs following the onset of puberty. en annan viktig bidragsgivare till vildsvin, skatole, kan också minskas som en indirekt effekt. aggressiva och sexuella (montering) beteenden minskar också. female pigs:induction of antibodies against gnrf to produce a temporary immunological suppression of ovarian function (suppression of oestrus) in order to reduce the incidence of unwanted pregnancies in gilts intended for slaughter, and to reduce the associated sexual behaviour (standing oestrus).

Europeiska unionen - svenska - EMA (European Medicines Agency)

united therapeutics europe ltd - dinutuximab - neuroblastom - antineoplastiska medel - unituxin är indicerat för behandling av högrisk neuroblastom hos patienter i åldern 12månader till 17år, som tidigare har mottagit induktionskemoterapi och uppnått minst ett delsvar, följt av myeloablativ terapi och autolog stamcellstransplantation transplantation (asct). det administreras i kombination med granulocyt-makrofagkolonistimulerande faktor (gm-csf), interleukin-2 (il-2) och isotretinoin.

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)

astrazeneca ab - andexanet alfa - drog-relaterade biverkningar och biverkningar - alla andra terapeutiska produkter - för vuxna patienter som behandlas med en direkt faktor xa (fxa) - hämmare (apixaban eller rivaroxaban) när återföring av antikoagulation som behövs på grund av livshotande eller okontrollerad blödning.

Europeiska unionen - svenska - EMA (European Medicines Agency)

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.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

galderma nordic ab - klobetasolpropionat - schampo - 500 mikrogram/g - etanol, vattenfri hjälpämne; klobetasolpropionat 500 mikrog aktiv substans - klobetasol

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

teva sweden ab - pamidronatdinatriumpentahydrat - koncentrat till infusionsvätska, lösning - 3 mg/ml - pamidronatdinatriumpentahydrat 2,527 mg aktiv substans - pamidronat

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

medac gesellschaft für klinische spezialpräparate mbh - pamidronatdinatrium, vattenfri - koncentrat till infusionsvätska, lösning - 3 mg/ml - pamidronatdinatrium, vattenfri 3 mg aktiv substans - pamidronat