Danimarka - Daniż - Lægemiddelstyrelsen (Danish Medicines Agency)

stada arzneimittel ag - montelukastnatrium - tyggetabletter - 5 mg

Unjoni Ewropea - Daniż - EMA (European Medicines Agency)

astrazeneca ab - acalabrutinib - leukæmi, lymfocytisk, kronisk, b-celle - antineoplastic agents, protein kinase inhibitors, - calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll). calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (cll) who have received at least one prior therapy.

Unjoni Ewropea - Daniż - EMA (European Medicines Agency)

accord healthcare s.l.u. - tolvaptan - uheldig adh-syndrom - diuretika, - tolvaptan is indicated in adults for the treatment of hyponatremia secondary to the syndrome of inappropriate antidiuretic hormone secretion (siadh).

Danimarka - Daniż - Lægemiddelstyrelsen (Danish Medicines Agency)

stada arzneimittel ag - fluconazol - kapsler, hårde - 150 mg

Danimarka - Daniż - Lægemiddelstyrelsen (Danish Medicines Agency)

stada arzneimittel ag - fluconazol - kapsler, hårde - 200 mg

Danimarka - Daniż - Lægemiddelstyrelsen (Danish Medicines Agency)

stada arzneimittel ag - lacosamid - filmovertrukne tabletter - 50 mg

Unjoni Ewropea - Daniż - EMA (European Medicines Agency)

cis bio international - samarium (153sm) lexidronam pentasodium - pain; cancer - terapeutiske radioaktive lægemidler - quadramet er indiceret til lindring af knoglesmerter hos patienter med flere smertefulde osteoblastic knogle metastaser, der fylder technetium [99mtc]-mærket biphosphonates på knoglescanning. tilstedeværelsen af osteoblastic metastaser, som kan tage op technetium [99mtc]-mærket biphosphonates skal være bekræftet forud for terapi.

Danimarka - Daniż - Lægemiddelstyrelsen (Danish Medicines Agency)

smartpractice denmark aps - alfa-amylcinnamaldehyd, bacitracin, benzocain, benzylparahydroxybenzoat, bronopol, budesonid, butylparahydroxybenzoat, chlorquinaldol, cinchocainhydrochlorid, cinnamaldehyd, cinnamylalkohol, clioquinol, cyclohexylbenzothiazylsulfenamid, diazolidinyl urea, dibenzothiazyldisulfid, dipentamethylenthiuramdisulfid, diphenylguanidin, disulfiram, epoxyresin, ethylendiamindihydrochlorid, ethylparahydroxybenzoat, eugenol, geraniol, guldsodiumthiosulphate, hydrocortisonbutyrat, hydroxycitronellal, imidazolidinyl urea - plaster til provokationstest

Unjoni Ewropea - Daniż - EMA (European Medicines Agency)

viiv healthcare b.v. - dolutegravir sodium, lamivudine, abacavir (as sulfate) - hiv infektioner - antivirale midler til systemisk anvendelse - triumeq is indicated for the treatment of human immunodeficiency virus (hiv) infected adults,  adolescents and children  weighing at least 25 kg who are antiretroviral treatment-naïve or are infected with hiv without documented or clinically suspected resistance to any of the three antiretroviral agents in triumeq.

Unjoni Ewropea - Daniż - EMA (European Medicines Agency)

n.v. organon - alendronsyre, colecalciferol - osteoporose, postmenopausale - narkotika til behandling af knoglesygdomme - behandling af postmenopausal osteoporose hos patienter med risiko for vitamin d-insufficiens. vantavo reducerer risikoen for vertebrale og hoftebrud. behandling af postmenopausal osteoporose hos patienter, der ikke får d-vitamin d-tilskud, og er i risiko for d-vitamin d-insufficiens. vantavo reducerer risikoen for vertebrale og hoftebrud.