Sverige - svensk - Läkemedelsverket (Medical Products Agency)

qdoxx pharma ab - felodipin; metoprololsuccinat - depottablett - 5 mg/50 mg - metoprololsuccinat 47,5 mg aktiv substans; laktos (vattenfri) hjälpämne; felodipin 5 mg aktiv substans; makrogolglycerolhydroxistearat hjälpämne - metoprolol och andra antihypertensiva medel

Sverige - svensk - Läkemedelsverket (Medical Products Agency)

qdoxx pharma ab - budesonid; formoterolfumaratdihydrat - inhalationspulver - 80 mikrogram/4,5 mikrogram/inhalation - formoterolfumaratdihydrat 4,5 mikrog aktiv substans; laktosmonohydrat hjälpämne; budesonid 80 mikrog aktiv substans - formoterol och budesonid

Den europeiske union - svensk - EMA (European Medicines Agency)

sanofi pasteur - influenza a virus subtype h1n1 haemagglutinin, recombinant, influenza a virus subtype h3n2 haemagglutinin, recombinant, influenza b virus victoria lineage haemagglutinin, recombinant, influenza b virus yamagata lineage haemagglutinin, recombinant - influensa, människa - vacciner - supemtek is indicated for active immunization for the prevention of influenza disease in adults. supemtek should be used in accordance with official recommendations.

Den europeiske union - svensk - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - nivolumab, relatlimab - melanom - antineoplastic agents, monoclonal antibodies - opdualag is indicated for the first line treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older with tumour cell pd l1 expression < 1%.

Den europeiske union - svensk - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - deucravacitinib - psoriasis - immunsuppressiva - treatment of moderate-to-severe plaque psoriasis in adults.

Sverige - svensk - myHealthbox

bayer ag -

Den europeiske union - svensk - EMA (European Medicines Agency)

beigene ireland ltd - zanubrutinib - waldenstrom macroglobulinemia - antineoplastiska medel - brukinsa as monotherapy is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. brukinsa as monotherapy is indicated for the treatment of adult patients with marginal zone lymphoma (mzl) who have received at least one prior anti-cd20-based therapy. brukinsa as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukemia (cll).

Sverige - svensk - myHealthbox

bayer ag -

Den europeiske union - svensk - EMA (European Medicines Agency)

seagen b.v. - tucatinib - breast neoplasms; neoplasm metastasis - antineoplastiska medel - tukysa is indicated in combination with trastuzumab and capecitabine for the treatment of adult patients with her2‑positive locally advanced or metastatic breast cancer who have received at least 2 prior anti‑her2 treatment regimens.

Sverige - svensk - Läkemedelsverket (Medical Products Agency)

orion corporation - budesonid; formoterolfumaratdihydrat - inhalationspulver - 160 mikrogram/4,5 mikrogram/inhalation - laktosmonohydrat hjälpämne; formoterolfumaratdihydrat 4,5 mikrog aktiv substans; budesonid 160 mikrog aktiv substans