ইউরোপীয় ইউনিয়ন - ডেনিশ - EMA (European Medicines Agency)

merck sharp & dohme b.v. - sugammadex - neuromuskulær blokade - alle andre terapeutiske produkter - tilbagevendelse af neuromuskulær blokade induceret af rocuronium eller vecuronium. for peadiatric befolkning: sugammadex er kun anbefales til rutinemæssig tilbageførsel af rocuronium-induceret blokade i børn og unge.

ইউরোপীয় ইউনিয়ন - ডেনিশ - EMA (European Medicines Agency)

merck sharp & dohme b.v. - indinavir-sulfat ethanolate - hiv infektioner - antivirale midler til systemisk anvendelse - crixivan er indiceret i kombination med antiretrovirale nukleosidanaloger til behandling af hiv-1-inficerede voksne.

ইউরোপীয় ইউনিয়ন - ডেনিশ - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - follitropin beta - infertility; hypogonadism - køn hormoner og modulatorer af den genitale system, - i den kvindelige:fertavid er indiceret til behandling af kvindelig infertilitet i følgende kliniske situationer:anovulation (herunder polycystisk ovarie sygdom, pcod) hos kvinder, der ikke har responderet på behandling med clomifene citratecontrolled æggestokkene hyperstimulation til at fremkalde udvikling af flere follikler i medicinsk assisteret reproduktion programmer [e. in vitro-fertilisering/ægoplægning (ivf/et), gamete intra-fallopian transfer (gave) og icsi (intracytoplasmic sperm injection). i den mandlige:mangelfuld spermatogenese på grund af hypogona.

ইউরোপীয় ইউনিয়ন - ডেনিশ - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - hepatitis b, rekombinant overflade antigen - hepatitis b; immunization - vacciner - 5 micrograms hbvaxpro is indicated for active immunisation against hepatitis-b-virus infection caused by all known subtypes in individuals from birth through 15 years of age considered at risk of exposure to hepatitis-b virus. den specifikke risiko-kategorier, der skal være vaccineret, skal der fastlægges på grundlag af de officielle anbefalinger. det kan forventes, at hepatitis d-virusset vil også forebygges ved vaccination med hbvaxpro som hepatitis d (forårsaget af delta-agent) ikke forekommer i mangel af hepatitis b infektion. 10 micrograms hbvaxpro is indicated for active immunisation against hepatitis-b-virus infection caused by all known subtypes in individuals 16 years of age or more considered at risk of exposure to hepatitis-b virus. den specifikke risiko-kategorier, der skal være vaccineret, skal der fastlægges på grundlag af de officielle anbefalinger. det kan forventes, at hepatitis d-virusset vil også forebygges ved vaccination med hbvaxpro som hepatitis d (forårsaget af delta-agent) ikke forekommer i mangel af hepatitis b infektion. 40 micrograms hbvaxpro is indicated for the active immunisation against hepatitis-b-virus infection caused by all known subtypes in predialysis and dialysis adult patients. det kan forventes, at hepatitis d-virusset vil også forebygges ved vaccination med hbvaxpro som hepatitis d (forårsaget af delta-agent) ikke forekommer i mangel af hepatitis b infektion.

ইউরোপীয় ইউনিয়ন - ডেনিশ - EMA (European Medicines Agency)

merck sharp dohme ltd - boceprevir - hepatitis c kronisk - antivirale midler til systemisk anvendelse - victrelis er indiceret til behandling af kronisk hepatitis-c (chc) genotype-1 infektion, kombineret med peginterferon alfa og ribavirin hos voksne patienter med kompenseret leversygdom som tidligere ubehandlet, eller der ikke har foregående terapi.

ইউরোপীয় ইউনিয়ন - ডেনিশ - EMA (European Medicines Agency)

merck sharp & dohme b.v. - virus, levende svækket, mæslinger, virus, levende svækkede, kusmaer, virus, levende svækket, rubella, virus, levende svækket, varicella - chickenpox; rubella; measles; mumps; immunization - vacciner - proquad er indiceret til samtidig vaccination mod mæslinger, fåresyge, røde hunde og varicella hos personer fra 12 måneder. proquad kan gives til personer, fra de er 9 måneder, alder under særlige omstændigheder (e. i overensstemmelse med national vaccination tidsplaner, udbrud situationer, eller rejse til et område med høj forekomst af mæslinger.

ডেনমার্ক - ডেনিশ - Lægemiddelstyrelsen (Danish Medicines Agency)

merck sharp & dohme b.v. - hepatitis a virus, stamme cr 326f (inaktiveret) - injektionsvæske, suspension, fyldt injektionssprøjte - 50 e./ml

ইউরোপীয় ইউনিয়ন - ডেনিশ - EMA (European Medicines Agency)

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic syre, sitagliptin fosfat monohydrat - diabetes mellitus, type 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - steglujan er indiceret hos voksne i alderen 18 år og ældre med type 2-diabetes som et supplement til kost og motion til forbedring af glykæmisk kontrol:når metformin og/eller et sulphonylurea (su) og en af de monocomponents af steglujan ikke giver tilstrækkelig glykæmisk kontrol. hos patienter, der allerede behandles med en kombination af ertugliflozin og sitagliptin som særskilte tabletter.

ইউরোপীয় ইউনিয়ন - ডেনিশ - 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 - antineoplastiske midler - 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 tumor mutationer, burde også have modtaget en målrettet behandling, før de modtager 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.

ইউরোপীয় ইউনিয়ন - ডেনিশ - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - temozolomid - glioma; glioblastoma - antineoplastiske midler - temodal hårde kapsler er indiceret til behandling af:voksne patienter med nyligt diagnosticerede glioblastoma multiforme samtidig med strålebehandling og efterfølgende som monoterapi behandling;børn fra en alder af tre år, unge og voksne patienter med ondartet gliom, såsom glioblastoma multiforme eller anaplastisk astrocytom, der viser recidiv eller progression efter standardbehandling.