Швеція - шведська - Läkemedelsverket (Medical Products Agency)

meda ab - acetylsalicylsyra - tablett - 500 mg - acetylsalicylsyra 500 mg aktiv substans

Швеція - шведська - myHealthbox

bayer ag -

Європейський Союз - шведська - EMA (European Medicines Agency)

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.

Швеція - шведська - Läkemedelsverket (Medical Products Agency)

virbac sa - fipronil - kutan spray, lösning - 2,5 mg/ml - fipronil 2,5 mg aktiv substans - fipronil - hund, katt

Швеція - шведська - Läkemedelsverket (Medical Products Agency)

bode chemie gmbh - isopropylalkohol; mecetroniumetilsulfat; propanol - kutan lösning - glycerol 85% hjälpämne; mecetroniumetilsulfat 2 mg aktiv substans; isopropylalkohol 450 mg aktiv substans; propanol 300 mg aktiv substans - kombinationer

Швеція - шведська - Läkemedelsverket (Medical Products Agency)

institut georges lopez - igl - glutaminsyra; glutation; histidin; kalciumkloriddihydrat; kaliumklorid; laktobionsyra; magnesiumkloridhexahydrat; mannitol; natriumhydroxid - vätska för organförvaring - laktobionsyra 28,664 g aktiv substans; glutaminsyra 2,942 g aktiv substans; natriumhydroxid 4 g aktiv substans; mannitol 10,93 g aktiv substans; glutation 0,921 g aktiv substans; histidin 4,65 g aktiv substans; kaliumklorid 1,118 g aktiv substans; magnesiumkloridhexahydrat 2,642 g aktiv substans; kalciumkloriddihydrat 0,037 g aktiv substans - spädningsvätskor och spolvätskor

Швеція - шведська - Läkemedelsverket (Medical Products Agency)

cis bio international - natriummolybdat(mo-99); natriumperteknetat(tc-99m) - radionuklidgenerator - 2 - 50 gbq - natriumperteknetat(tc-99m) 2 - 50 gbq aktiv substans; natriummolybdat(mo-99) 2,5 - 60 gbq aktiv substans - teknetium(tc-99m)perteknetat

Швеція - шведська - Läkemedelsverket (Medical Products Agency)

ge healthcare b.v. - natriummolybdat(mo-99); natriumperteknetat(tc-99m) - radionuklidgenerator - 2,5-100 gbq - natriumperteknetat(tc-99m) aktiv substans; natriummolybdat(mo-99) 2,5 - 100 gbq aktiv substans - teknetium(tc-99m)perteknetat

Європейський Союз - шведська - EMA (European Medicines Agency)

pierre fabre medicament - vinflunin - carcinoma, transitional cell; urologic neoplasms - antineoplastiska medel - javlor indikeras i monoterapi för behandling av vuxna patienter med avancerat eller metastatiskt övergångscellskarcinom i uroteletten efter misslyckande av en tidigare platinhaltig behandling. effekt och säkerhet av vinflunine har inte studerats på patienter med performance status ≥ 2.

Європейський Союз - шведська - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - nivolumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; mesothelioma; colorectal neoplasms - antineoplastiska medel - melanomaopdivo as monotherapy or in combination with ipilimumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older. relative to nivolumab monotherapy, an increase in progression free survival (pfs) and overall survival (os) for the combination of nivolumab with ipilimumab is established only in patients with low tumour pd-l1 expression. adjuvant treatment of melanomaopdivo as monotherapy is indicated for the adjuvant treatment of adults and adolescents 12 years of age and older with melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection. non-small cell lung cancer (nsclc)opdivo in combination with ipilimumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising egfr mutation or alk translocation. opdivo as monotherapy is indicated for the treatment of locally advanced or metastatic non-small cell lung cancer after prior chemotherapy in adults. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. malignant pleural mesothelioma (mpm)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. renal cell carcinoma (rcc)opdivo as monotherapy is indicated for the treatment of advanced renal cell carcinoma after prior therapy in adults. opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with intermediate/poor risk advanced renal cell carcinoma. opdivo in combination with cabozantinib is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma. classical hodgkin lymphoma (chl)opdivo as monotherapy is indicated for the treatment of adult patients with relapsed or refractory classical hodgkin lymphoma after autologous stem cell transplant (asct) and treatment with brentuximab vedotin. squamous cell cancer of the head and neck (scchn)opdivo as monotherapy is indicated for the treatment of recurrent or metastatic squamous cell cancer of the head and neck in adults progressing on or after platinum based therapy. urothelial carcinomaopdivo as monotherapy is indicated for the treatment of locally advanced unresectable or metastatic urothelial carcinoma in adults after failure of prior platinum containing therapy. adjuvant treatment of urothelial carcinomaopdivo as monotherapy is indicated for the adjuvant treatment of adults with muscle invasive urothelial carcinoma (miuc) with tumour cell pd-l1 expression ≥ 1%, who are at high risk of recurrence after undergoing radical resection of miuc. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)opdivo in combination with ipilimumab is indicated for the treatment of adult patients with mismatch repair deficient or microsatellite instability-high metastatic colorectal cancer after prior fluoropyrimidine based combination chemotherapy. oesophageal squamous cell carcinoma (oscc)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%. opdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%. opdivo as monotherapy is indicated for the treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma after prior fluoropyrimidine- and platinum-based combination chemotherapy. adjuvant treatment of oesophageal or gastro-oesophageal junction cancer (oc or gejc)opdivo as monotherapy is indicated for the adjuvant treatment of adult patients with oesophageal or gastro-oesophageal junction cancer who have residual pathologic disease following prior neoadjuvant chemoradiotherapy. gastric, gastro‑oesophageal junction (gej) or oesophageal adenocarcinomaopdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first‑line treatment of adult patients with her2‑negative advanced or metastatic gastric, gastro‑oesophageal junction or oesophageal adenocarcinoma whose tumours express pd-l1 with a combined positive score (cps) ≥ 5.