Europeiska unionen - svenska - EMA (European Medicines Agency)

roche registration gmbh - atezolizumab - carcinoma, transitional cell; carcinoma, non-small-cell lung; urologic neoplasms; breast neoplasms; small cell lung carcinoma - antineoplastiska medel - urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or - who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancer tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated for the first-line treatment of adult patients with metastatic non-squamous non small cell lung cancer (nsclc). in patients with egfr mutant or alk-positive nsclc, tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated only after failure of appropriate targeted therapies (see section 5. tecentriq, in combination with nab paclitaxel and carboplatin, is indicated for the first line treatment of adult patients with metastatic non-squamous nsclc who do not have egfr mutant or alk positive nsclc (see section 5. tecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq som monoterapi är indicerat för behandling av vuxna patienter med lokalt avancerad eller metastaserad icke-småcellig lungcancer efter tidigare kemoterapi. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. small cell lung cancertecentriq, in combination with carboplatin and etoposide, is indicated for the first-line treatment of adult patients with extensive-stage small cell lung cancer (es-sclc) (see section 5. hepatocellular carcinomatecentriq, in combination with bevacizumab, is indicated for the treatment of adult patients with advanced or unresectable hepatocellular carcinoma (hcc) who have not received prior systemic therapy (see section 5. urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or- who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancertecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq som monoterapi är indicerat för behandling av vuxna patienter med lokalt avancerad eller metastaserad icke-småcellig lungcancer efter tidigare kemoterapi. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. triple-negative breast cancertecentriq in combination with nab-paclitaxel is indicated for the treatment of adult patients with unresectable locally advanced or metastatic triple-negative breast cancer (tnbc) whose tumours have pd-l1 expression ≥ 1% and who have not received prior chemotherapy for metastatic disease.

Europeiska unionen - svenska - EMA (European Medicines Agency)

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - diabetes mellitus, typ 2 - läkemedel som används vid diabetes - for adult patients with type 2 diabetes mellitus:it is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. it is indicated in combination with a sulphonylurea (i. - , trippel kombinationsterapi) som ett komplement till kost och motion hos patienter bristfälligt kontrollerad på deras maximal tolererad dos av metformin och en sulphonylurea. it is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparγ agonist. it is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

cogmill pharma ab - järn(ii)glycinsulfat - enterokapsel, hård - 100 mg - järn(ii)glycinsulfat 567,66 mg aktiv substans; natriumlaurilsulfat hjälpämne - järn(ii)glycinsulfat

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

evolan pharma ab - ketokonazol - schampo - 20 mg/g - ketokonazol 20 mg aktiv substans; bensylalkohol hjälpämne - ketokonazol

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

xvivo perfusion ab - dextran 40; dinatriumfosfatdodekahydrat; glukosmonohydrat; kaliumdivätefosfat; kaliumklorid; magnesiumsulfatheptahydrat; natriumklorid - vätska för organförvaring - dinatriumfosfatdodekahydrat 117 mikrog aktiv substans; magnesiumsulfatheptahydrat 200 mikrog aktiv substans; kaliumklorid 400 mikrog aktiv substans; natriumklorid 8 mg aktiv substans; kaliumdivätefosfat 63 mikrog aktiv substans; dextran 40 50 mg aktiv substans; glukosmonohydrat 1 mg aktiv substans - Övriga icke terapeutiska hjälpmedel

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

bristol-myers squibb ab - adenosin; allopurinol; glutation; hydroxietylstärkelse, 250/0.45; kaliumdivätefosfat; kaliumhydroxid; laktobionsyra; magnesiumsulfatheptahydrat; natriumhydroxid; raffinospentahydrat - vätska för organförvaring - hydroxietylstärkelse, 250/0.45 50 mg aktiv substans; adenosin 1,34 mg aktiv substans; allopurinol 136 mikrog aktiv substans; glutation 922 mikrog aktiv substans; raffinospentahydrat 17,83 mg aktiv substans; magnesiumsulfatheptahydrat 1,23 mg aktiv substans; kaliumdivätefosfat 3,4 mg aktiv substans; kaliumhydroxid 5,611 mg aktiv substans; natriumhydroxid 1,08 mg aktiv substans; laktobionsyra 35,83 mg aktiv substans - spädningsvätskor och spolvätskor

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

salus haus gmbh & co kg - pimpinella anisum (anis) frukt / carum carvi (kummin) frukt / foeniculum vulgare (bitterfänkål) frukt / polygonum aviculare (trampört) ört / tilia cordata (lind) blomma / thymus vulgaris (timjan) ört; vattendestillat; bergtallolja; bitterfänkålsolja; citronolja; eukalyptusolja; pepparmyntolja; stjärnanisolja - sirap - pimpinella anisum (anis) frukt / carum carvi (kummin) frukt / foeniculum vulgare (bitterfänkål) frukt / polygonum aviculare (trampört) ört / tilia cordata (lind) blomma / thymus vulgaris (timjan) ört; vattendestillat 192,53 mg aktiv substans; sackaros hjälpämne; etanol, vattenfri hjälpämne; bitterfänkålsolja 0,15 mg aktiv substans; stjärnanisolja 0,15 mg aktiv substans; eukalyptusolja 0,09 mg aktiv substans; pepparmyntolja 0,09 mg aktiv substans; bergtallolja 0,71 mg aktiv substans; citronolja 0,26 mg aktiv substans - medel mot hosta och förkylning

Europeiska unionen - svenska - EMA (European Medicines Agency)

lantheus eu limited - perflutren - ekokardiografi - kontrastmedia - detta läkemedel är endast för diagnostisk användning. luminity är ett ultraljud kontrast-för att öka agent för användning i patienter i vilka icke-kontrast ekokardiografi var suboptimal (suboptimal anses tyda på att åtminstone två av sex segment i den 4 - eller 2-avdelningen bild av ventrikulär gränsen var inte utvärderingsbara) och som har misstänkt eller etablerad kranskärlssjukdom, för att ge grumling av hjärtats kamrar och förbättring av vänster kammare endocardial border avgränsning vid både vila och stress.

Europeiska unionen - svenska - EMA (European Medicines Agency)

cis bio international  - besilesomab - osteomyelitis; radionuclide imaging - diagnostiska radioaktiva läkemedel - detta läkemedel är endast avsett för diagnostik och den godkända indikationen är scintigrafisk avbildning, tillsammans med andra lämpliga avbildningsmetoder, för fastställandet av lokalisering av inflammation/infektion i perifera ben hos vuxna med misstänkt osteomyelit. scintimun ska inte användas för diagnos av diabetisk fotinfektion.

Europeiska unionen - svenska - EMA (European Medicines Agency)

astrazeneca ab - durvalumab - carcinom, non-small cell lung - antineoplastiska medel - non-small cell lung cancer (nsclc)imfinzi as monotherapy is indicated for the treatment of locally advanced, unresectable non small cell lung cancer (nsclc) in adults whose tumours express pd-l1 on ≥ 1% of tumour cells and whose disease has not progressed following platinum based chemoradiation therapy (see section 5. imfinzi in combination with tremelimumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic nsclc with no sensitising egfr mutations or alk positive mutations. small cell lung cancer (sclc)imfinzi in combination with etoposide and either carboplatin or cisplatin is indicated for the first-line treatment of adults with extensive-stage small cell lung cancer (es-sclc). biliary tract cancer (btc)imfinzi in combination with gemcitabine and cisplatin is indicated for the first line treatment of adults with unresectable or metastatic biliary tract cancer (btc). hepatocellular carcinoma (hcc)imfinzi in combination with tremelimumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc).