Europeiska unionen - svenska - EMA (European Medicines Agency)

novo nordisk a/s - repaglinid - diabetes mellitus, typ 2 - läkemedel som används vid diabetes - repaglinid är indicerat för patienter med typ 2-diabetes (icke-insulinberoende diabetes mellitus (niddm)) vars hyperglykemi kan inte längre kontrolleras tillfredsställande av diet, viktreduktion och motion. repaglinid är också indicerat i kombination med metformin hos patienter med typ 2-diabetes som inte kontrolleras på ett tillfredsställande sätt på metformin ensam. behandling bör initieras som ett komplement till diet och motion för att sänka blodsockret i förhållande till måltider.

Europeiska unionen - svenska - EMA (European Medicines Agency)

novo nordisk a/s - repaglinid - diabetes mellitus, typ 2 - läkemedel som används vid diabetes - repaglinid är indicerat för patienter med typ 2-diabetes (icke-insulinberoende diabetes mellitus (niddm)) vars hyperglykemi kan inte längre kontrolleras tillfredsställande av diet, viktreduktion och motion. repaglinid är också indicerat i kombination med metformin hos patienter med typ 2-diabetes som inte kontrolleras på ett tillfredsställande sätt på metformin ensam. behandling bör initieras som ett komplement till diet och motion för att sänka blodsockret i förhållande till måltider.

Europeiska unionen - svenska - EMA (European Medicines Agency)

merck sharp & dohme b.v. - pembrolizumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; endometrial neoplasms - antineoplastiska medel - melanomakeytruda as monotherapy is indicated for the treatment of adults and adolescents aged 12 years and older with advanced (unresectable or metastatic) melanoma. keytruda as monotherapy is indicated for the adjuvant treatment of adults and adolescents aged 12 years and older with stage iib, iic, or with stage iii melanoma and lymph node involvement who have undergone complete resection. non small cell lung carcinoma (nsclc)keytruda as monotherapy is indicated for the adjuvant treatment of adults with non-small cell lung carcinoma who are at high risk of recurrence following complete resection and platinum based chemotherapy (for selection criteria, see section 5. keytruda as monotherapy is indicated for the first line treatment of metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 50% tumour proportion score (tps) with no egfr or alk positive tumour mutations. keytruda, in combination with pemetrexed and platinum chemotherapy, is indicated for the first-line treatment of metastatic non squamous non small cell lung carcinoma in adults whose tumours have no egfr or alk positive mutations. keytruda, in combination with carboplatin and either paclitaxel or nab paclitaxel, is indicated for the first line treatment of metastatic squamous non small cell lung carcinoma in adults. keytruda  as monotherapy is indicated for the treatment of locally advanced or metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 1% tps and who have received at least one prior chemotherapy regimen. patienter med egfr eller alk-positiv tumör mutationer bör också ha fått riktad terapi innan du tar emot keytruda. classical hodgkin lymphoma (chl)keytruda as monotherapy is indicated for the treatment of adult and paediatric patients aged 3 years and older with relapsed or refractory classical hodgkin lymphoma who have failed autologous stem cell transplant (asct) or following at least two prior therapies when asct is not a treatment option. urothelial carcinomakeytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who have received prior platinum containing chemotherapy. keytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who are not eligible for cisplatin containing chemotherapy and whose tumours express pd l1 with a combined positive score (cps) ≥ 10. head and neck squamous cell carcinoma (hnscc)keytruda, as monotherapy or in combination with platinum and 5 fluorouracil (5 fu) chemotherapy, is indicated for the first line treatment of metastatic or unresectable recurrent head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a cps ≥ 1. keytruda as monotherapy is indicated for the treatment of recurrent or metastatic head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a ≥ 50% tps and progressing on or after platinum containing chemotherapy. renal cell carcinoma (rcc)keytruda, in combination with axitinib, is indicated for the first line treatment of advanced renal cell carcinoma in adults. keytruda  as monotherapy is indicated for the adjuvant treatment of adults with renal cell carcinoma at increased risk of recurrence following nephrectomy, or following nephrectomy and resection of metastatic lesions (for selection criteria, please see section 5. microsatellite instability high (msi-h) or mismatch repair deficient (dmmr) cancerscolorectal cancer (crc)keytruda as monotherapy is indicated for theadults with msi-h or dmmr colorectal cancer in the following settings:first line treatment of metastatic microsatellite instability high (msi h) or mismatch repair deficient (dmmr) colorectal cancer in adults;treatment of unresectable or metastatic colorectal cancer after previous fluoropyrimidine based combination therapy.  non-colorectal cancerskeytruda as monotherapy is indicated for the treatment of the following msi h or dmmr tumours in adults with:advanced or recurrent endometrial carcinoma, who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation;unresectable or metastatic gastric, small intestine, or biliary cancer, who have disease progression on or following at least one prior therapy. oesophageal carcinomakeytruda, in combination with platinum and fluoropyrimidine based chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic carcinoma of the oesophagus or her-2 negative gastroesophageal junction adenocarcinoma, in adults whose tumours express pd l1 with a cps ≥ 10. triple negative breast cancer (tnbc)keytruda, in combination with chemotherapy as neoadjuvant treatment, and then continued as monotherapy as adjuvant treatment after surgery, is indicated for the treatment of adults with locally advanced, or early stage triple negative breast cancer at high risk of recurrence. keytruda, in combination with chemotherapy, is indicated for the treatment of locally recurrent unresectable or metastatic triple negative breast cancer in adults whose tumours express pd l1 with a cps ≥ 10 and who have not received prior chemotherapy for metastatic disease. endometrial carcinoma (ec)keytruda, in combination with lenvatinib, is indicated for the treatment of advanced or recurrent endometrial carcinoma in adults who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation. cervical cancerkeytruda, in combination with chemotherapy with or without bevacizumab, is indicated for the treatment of persistent, recurrent, or metastatic cervical cancer in adults whose tumours express pd l1 with a cps ≥ 1. gastric or gastro-oesophageal junction (gej) adenocarcinomakeytruda, in combination with trastuzumab, fluoropyrimidine and platinum-containing chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic her2-positive gastric or gastro-oesophageal junction adenocarcinoma in adults whose tumours express pd-l1 with a cps ≥ 1.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ge healthcare as - gadoterinsyra - injektionsvätska, lösning - 0,5 mmol/ml - gadoterinsyra 279,32 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ge healthcare as - gadoterinsyra - injektionsvätska, lösning i förfylld spruta - 0,5 mmol/ml - gadoterinsyra 279,32 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

norbrook laboratories (ireland) limited - flunixinmeglumin - granulat - 250 mg - laktosmonohydrat hjälpämne; sackaros hjälpämne; flunixinmeglumin 415 mg aktiv substans - flunixin - häst

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ceva santé animale - flunixinmeglumin - injektionsvätska, lösning - 50 mg/ml - flunixinmeglumin 50 mg aktiv substans; propylenglykol hjälpämne - flunixin - häst, nöt, svin

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

intervet international b.v. - flunixinmeglumin - pour-on, lösning - 50 mg/ml - flunixinmeglumin 83 mg aktiv substans; propylenglykoldikaprylokaprat hjälpämne; allurarött ac hjälpämne - flunixin - nöt

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

natumin pharma ab - zea mays (majs) pollen och pistill / secale cereale (råg) pollen / dactylis glomerata (hundäxing) pollen / pinus sylvestris (tall) pollen; extrakt - filmdragerad tablett - zea mays (majs) pollen och pistill / secale cereale (råg) pollen / dactylis glomerata (hundäxing) pollen / pinus sylvestris (tall) pollen; extrakt 68 mg aktiv substans - psykoanaleptika

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

natumin pharma ab - secale cereale (råg) / phleum pratense (timotej) / zea mays (majs) pollen; tjockt extrakt (25:1); aceton; (ea5); secale cereale (råg) / phleum pratense (timotej) / zea mays (majs) pollen; torrt extrakt (1,1-1,4:1); aceton 5 %; (p2); extraktet innehåller 45,1 mg hjälpämnen. - filmdragerad tablett - laktosmonohydrat hjälpämne; secale cereale (råg) / phleum pratense (timotej) / zea mays (majs) pollen; tjockt extrakt (25:1); aceton; (ea5) 4 mg aktiv substans; secale cereale (råg) / phleum pratense (timotej) / zea mays (majs) pollen; torrt extrakt (1,1-1,4:1); aceton 5 %; (p2); extraktet innehåller 45,1 mg hjälpämnen. 70 mg aktiv substans - urologiska medel