Reagila Den europeiske union - dansk - EMA (European Medicines Agency)

reagila

gedeon richter - cariprazinhydrochlorid - skizofreni - psykoleptika - reagila er indiceret til behandling af skizofreni hos voksne patienter.

Pelmeg Den europeiske union - dansk - EMA (European Medicines Agency)

pelmeg

mundipharma corporation (ireland) limited - pegfilgrastim - neutropeni - immunostimulants, - til at reducere varigheden af neutropeni og forekomsten af febril neutropeni på grund af kemoterapi.

Verzenios Den europeiske union - dansk - EMA (European Medicines Agency)

verzenios

eli lilly nederland b.v. - abemaciclib - bryst neoplasmer - antineoplastiske midler - early breast cancerverzenios in combination with endocrine therapy is indicated for the adjuvant treatment of adult patients with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative, node positive early breast cancer at high risk of recurrence (see section 5. in pre or perimenopausal women, aromatase inhibitor endocrine therapy should be combined with a luteinising hormone-releasing hormone (lhrh) agonist. advanced or metastatic breast cancerverzenios is indicated for the treatment of women with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant as initial endocrine-based therapy, or in women who have received prior endocrine therapy. in pre- or perimenopausal women, the endocrine therapy should be combined with a lhrh agonist.

Emgality Den europeiske union - dansk - EMA (European Medicines Agency)

emgality

eli lilly nederland b.v. - galcanezumab - migræneforstyrrelser - analgesics, galcanezumab - emgality er indiceret til forebyggelse af migræne hos voksne, der har mindst 4 migræne dage per måned.

Efavirenz/Emtricitabine/Tenofovir disoproxil "Glenmark" 600+200+245 mg filmovertrukne tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

efavirenz/emtricitabine/tenofovir disoproxil "glenmark" 600+200+245 mg filmovertrukne tabletter

glenmark arzneimittel gmbh - efavirenz, emtricitabin, tenofovirdisoproxilfumarat - filmovertrukne tabletter - 600+200+245 mg

Cegfila (previously Pegfilgrastim Mundipharma) Den europeiske union - dansk - EMA (European Medicines Agency)

cegfila (previously pegfilgrastim mundipharma)

mundipharma corporation (ireland) limited - pegfilgrastim - neutropeni - immunostimulants, - reduktion i varigheden af neutropeni og forekomst af febril neutropeni hos voksne patienter behandlet med cytotoksisk kemoterapi for malignitet (med undtagelse af kronisk myeloid leukæmi og myelodysplastisk syndromer).

Baqsimi Den europeiske union - dansk - EMA (European Medicines Agency)

baqsimi

eli lilly nederland b.v. - glucagon - diabetes mellitus - pancreas hormoner, hormoner glycogenolytic - baqsimi er indiceret til behandling af alvorlig hypoglykæmi hos voksne, unge og børn i alderen 4 år og derover med diabetes mellitus.

Lyumjev (previously Liumjev) Den europeiske union - dansk - EMA (European Medicines Agency)

lyumjev (previously liumjev)

eli lilly nederland b.v. - insulin lispro - diabetes mellitus - narkotika anvendt i diabetes - behandling af diabetes mellitus hos voksne, unge og børn i alderen 1 år og derover. behandling af diabetes mellitus hos voksne.

Retsevmo Den europeiske union - dansk - EMA (European Medicines Agency)

retsevmo

eli lilly nederland b.v. - selpercatinib - carcinoma, non-small-cell lung; thyroid neoplasms - antineoplastiske midler - retsevmo as monotherapy is indicated for the treatment of adults and adolescents 12 years and older with advanced ret-mutant medullary thyroid cancer (mtc)advanced ret fusion-positive non-small cell lung cancer (nsclc) not previously treated with a ret inhibitoradvanced ret fusion-positive thyroid cancer who require systematic therapy following prior treatment.

Mounjaro Den europeiske union - dansk - EMA (European Medicines Agency)

mounjaro

eli lilly nederland b.v. - tirzepatide - diabetes mellitus, type 2 - narkotika anvendt i diabetes - mounjaro is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance or contraindications- in addition to other medicinal products for the treatment of diabetes. for study results with respect to combinations, effects on glycaemic control and the populations studied, see sections 4. 4, 4. 5 og 5.